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Rimonabant (SR141716) Cannabinoid Receptor antagonista

Name: Rimonabant (SR141716)
Brand: Selleck Chemicals
SKU: S3021
Rating: 5 (8 reviews)

Cat. No.S3021

Rimonabant (SR141716) es un antagonista selectivo del CB1 con una IC50 de 13,6 nM y una EC50 de 17,3 nM en membranas de HEK 293 transfectadas con hCB1, y también es un inhibidor dual de las acil CoA:colesterol aciltransferasas (ACAT) 1 y 2 que inhibe la MmpL3 micobacteriana.

Rimonabant (SR141716) Cannabinoid Receptor antagonista Chemical Structure

Estructura química

Peso molecular: 463.79

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Control de calidad

Lote: Pureza: 99.67%

99.67

Dianas relacionadas	CXCR Hedgehog/Smoothened PKA Adrenergic Receptor AChR 5-HT Receptor Histamine Receptor Dopamine Receptor Ras KRas
Otros Cannabinoid Receptor Inhibidores	AM1241 AM251 BML-190 Otenabant (CP-945598) HCl 6-Iodopravadoline (AM630) Org 27569 GW842166X CID16020046 WIN 55, 212-2 mesylate Yangonin

Cultivo celular, tratamiento y concentración de trabajo

Líneas celulares	Tipo de ensayo	Concentración	Tiempo de incubación	Descripción de la actividad	PMID
CHO cells	Function assay			Ability to displace [3H]-SR- 141716A binding to human CB1 receptor expressed in CHO cell membranes, Ki=8.9 nM	10465552
CHO	Function assay			Antagonistic activity towards cannabinoid receptor 1 expressed as [3H]Arachidonic acid release in CHO cells, Kd=0.002512μM	14736243
CHO	Function assay			Displacement of CP-55940 binding from recombinant human cannabinoid receptor 1 expressed in CHO cells, Ki=0.025μM	14736243
CHO	Function assay			Affinity to displace CP-55940 binding from Cannabinoid receptor 2 of human expressed in CHO cells, Ki=1.58μM	14736243
CHO	Function assay			Inhibitory concentration against human recombinant cannabinoid receptor type 1 expressed in Chinese Hamster Ovary (CHO) cells, IC50=0.006μM	15713403
CHO	Function assay			In vitro cannabinoid receptor 1 antagonism of [3H]arachidonic acid release by CHO cells, Kd=0.002512μM	15771428
CHO	Function assay			In vitro displacement of CP-55940 binding to human CB1 receptor expressed in CHO cells, Ki=0.025μM	15771428
CHO	Function assay			In vitro displacement of CP-55940 binding to human CB2 receptor expressed in CHO cells, Ki=1.58μM	15771428
CHO	Function assay			Inhibition of [3H]SR-141,716A binding to human CB1 receptor expressed in CHO cells, Ki=0.0054μM	15801840
CHO	Function assay			Antagonistic activity against cannabinoid receptor 1 measured by CP-55940 induced arachnoid acid release in CHO cells, Kd=0.002512μM	16140010
CHO	Function assay			Displacement of specific CP-55940 binding in CHO cells stably transfected with human cannabinoid receptor 1, Ki=0.025μM	16140010
CHO	Function assay			Displacement of specific CP-55940 binding in CHO cells stably transfected with human cannabinoid receptor 2, Ki=1.58μM	16140010
CHOK1	Function assay			Functional activity at human CB1 receptor transfected in CHOK1 cells by [35SGTP]gammaS assay, Ki=0.001μM	16263283
HEK293	Function assay			Displacement of [3H]SR-141716 from human CB1 receptor transfected in HEK293 cells, Ki=0.0021μM	16263283
CHO	Function assay			Displacement of [3H]SR141716A from human CB1 receptor expressed in CHO cells, Ki=0.0054μM	16279809
HEK293	Function assay			Displacement of [3H]SR-141716 from human CB1 receptor expressed in HEK293 cells, Kd=0.0018μM	17004712
HEK293	Function assay			Displacement of [3H]CP-55940 from human CB1 receptor expressed in HEK293 cells, Ki=0.0071μM	17004712
HEK293	Function assay			Displacement of [3H]WIN-55212-2 from human CB1 receptor expressed in HEK293 cells, Ki=0.018μM	17004712
CHO	Function assay			Inhibition of [3H]CP-55940 binding to human recombinant CB1 receptor in CHO cells, IC50=0.0061μM	17181138
CHO	Function assay			Inhibition of [3H]CP-55940 binding to human recombinant CB2 receptor in CHO cells, IC50=0.6μM	17181138
CHO	Function assay			Displacement of [3H]CP-55940 from human recombinant CB1 receptor expressed in CHO cells, IC50=0.0061μM	17293109
CHO	Function assay			Displacement of [3H]CP-55940 from human recombinant CB2 receptor expressed in CHO cells, IC50=0.6033μM	17293109
HEK293	Function assay			Displacement of [3H]CP-559440 from human CB1 receptor expressed in HEK293 cells, Ki=0.0011μM	17383180
HEK293	Function assay			Displacement of [3H]CP-55940 from human recombinant CB1 receptor expressed in HEK293 cells, Ki=0.016μM	17942307
HEK293	Function assay			Displacement of [3H]CP-55940 from human recombinant CB2 receptor expressed in HEK293 cells, Ki=1.64μM	17942307
HEK293	Function assay			Displacement of [3H]CP-55940 from human recombinant CB1 receptor expressed in HEK293 cells, Ki=0.047μM	17979261
CHOK1	Function assay			Displacement of [3H]WIN-552122 from human recombinant CB2 receptor expressed in CHOK1 cells, Ki=1.99μM	17979261
HEK293	Function assay			Displacement of radioligand from human CB1 receptor expressed in HEK293 cells, Ki=0.0018μM	18083560
HEK293 EBNA	Function assay			Inverse agonist activity at human CB1 receptor expressed in HEK293 EBNA cells by [35S]GTPgammaS incorporation assay, EC50=0.004μM	18083560
HEK293	Function assay			Displacement of radioligand from human CB2 receptor expressed in HEK293 cells, Ki=0.554μM	18083560
CHOK1	Function assay			Antagonist activity at human CB1 receptor expressed in CHOK1 cells by luciferase assay, IC50=0.12μM	18243711
CHOK1	Function assay			Displacement of [3H]WIN-55212-2 from human CB2 receptor expressed in CHOK1 cells, IC50=1.76μM	18243711
HEK	Function assay			Displacement of [3H]CP-55940 from human recombinant CB1 receptor expressed in HEK cells, Ki=0.012μM	18293908
HEK	Function assay			Displacement of [3H]CP-55940 from human recombinant CB2 receptor expressed in HEK cells, Ki=0.79μM	18293908
HEK293	Function assay			Displacement of [3H]CP-55940 from human CB1R expressed in HEK293 cells, Ki=0.006μM	18335976
CHO	Function assay			Displacement of [3H]WIN-55212-2 from human cannabinoid CB2 receptor expressed in CHO cells, IC50=1.76μM	18337096
CHO	Function assay			Displacement of [3H]CP-55940 from human CB1 receptor expressed in CHO cells, Ki=0.025μM	18342403
CHO	Function assay			Displacement of [3H]WIN-55212-2 from human CB2 receptor expressed in CHO cells, Ki=1.58μM	18342403
HEK293	Function assay			Displacement of [3H]CP-55940 from human CB1 receptor expressed in HEK293 cells, Ki=0.0024μM	18363352
CHO	Function assay			Displacement of [3H]CP-55940 from human CB2 receptor expressed in CHO cells, Ki=0.56μM	18363352
SF9	Function assay			Antagonist activity at rat CB1 receptor in SF9 cells assessed as inhibition of CP-55940-stimulated GTPgammaS binding, Ki=0.00031μM	18448340
SF9	Function assay			Antagonist activity at human CB1 receptor expressed in SF9 cells assessed as inhibition of CP-55940-stimulated GTPgammaS binding, Ki=0.00043μM	18448340
SF9	Function assay			Inverse agonist at human CB1 receptor expressed in SF9 cells assessed as decrease in GTPgammaS level, IC50=0.00135μM	18448340
SF9	Function assay			Antagonist activity at human CB2 receptor in SF9 cells assessed as inhibition of CP-55940-stimulated GTPgammaS binding, Ki=0.815μM	18448340
HEK293	Function assay			Displacement of [3H]CP-55940 form human recombinant CB1 receptor expressed in HEK293 cells by liquid scintillation counting, Ki=0.04μM	18511157
CHO-K1	Function assay			Displacement of [3H]SR141716 from human CB1 receptor expressed in CHO-K1 cells, Ki=0.00118μM	18512901
HEK293	Function assay			Antagonist activity at human CB1 receptor expressed in HEK293 cells assessed as inhibition of CP-55940-stimulated [35S]GTPgammaS binding, Kd=0.00257μM	18512901
HEK293	Function assay			Displacement of [3H]CP-55940 from human CB1 receptor expressed in HEK293 cells, Ki=0.00618μM	18512901
CHO-K1	Function assay			Displacement of [3H]CP-55940 from human CB2 receptor expressed in CHO-K1 cells, Ki=0.313μM	18512901
HEK	Function assay			Displacement of [3H]CP-55940 from human recombinant CB1 receptor expressed in HEK cells, Ki=0.008μM	18579386
HEK	Function assay			Displacement of [3H]CP-55940 from human recombinant CB2 receptor expressed in HEK cells, Ki=0.79μM	18579386
HEK293	Function assay			Displacement of [3H]CP-55940 from human CB1 receptor expressed in HEK293 cells, Ki=0.012μM	18680276
HEK293	Function assay			Displacement of [3H]CP-55940 from human CB2 receptor expressed in HEK293 cells, Ki=0.79μM	18680276
HEK293	Function assay			Displacement of [3H]CP-55940 from human CB1 receptor expressed in HEK293 cells, IC50=0.015μM	18712856
HEK293	Function assay			Antagonist activity at human CB1 receptor expressed in HEK293 cells assessed as inhibition of Eu-GTP binding, EC50=0.0182μM	18712856
HEK293	Function assay			Displacement of [3H]CP-55940 from human CB2 receptor expressed in HEK293 cells, IC50=1.9398μM	18712856
HEK293	Function assay			Inverse agonist activity at human CB1 receptor expressed in HEK293 cells assessed as decrease in [35S]gammaGTP binding relative to control	18712856
CHO	Function assay			Antagonist activity at human CB1 receptor in CHO cells assessed as GTPgammaS binding, Kb=0.000698μM	18800770
CHOK1	Function assay			Displacement of [3H]WIN-55212-2 from human CB2 receptor expressed in CHOK1 cells by liquid scintillation spectrometry, IC50=1.76μM	18954042
CHO	Function assay			Displacement of [3H]WIN-55212-2 from human CB2 receptor expressed in CHO cells, IC50=1.76μM	19022666
HEK293	Function assay			Displacement of [3H]CP-55940 from human CB2 receptor expressed in HEK293 cells, IC50=0.0019μM	19095444
HEK293	Function assay			Displacement of [3H]CP-55940 from human CB1 receptor expressed in HEK293 cells, IC50=0.015μM	19095444
HEK293	Function assay			Antagonist activity at human CB1 receptor expressed in HEK293 cells assessed as inhibition of Eu-GTP binding, EC50=0.0182μM	19095444
CHO-K1	Function assay			Antagonist activity against human CB1 receptor expressed in CHO-K1 cells by [35S]GTPgamma binding assay, Ki=0.00019μM	19102698
HEK293	Function assay			Displacement of [3H]SR141716A from human CB1 receptor expressed in HEK293 cells, Ki=0.0009μM	19102698
CHOK1	Function assay			Displacement of [3H]WIN-55212-2 from human recombinant cannabinoid CB2 receptor expressed in CHOK1 cells by liquid scintillation spectrometry, IC50=1.76μM	19269817
CHOK1	Function assay			Antagonist activity at human cannabinoid CB1 receptor expressed in CHOK1 cells assessed as cAMP activity, EC50=0.24μM	19328683
CHOK1	Function assay			Antagonist activity at human cannabinoid CB2 receptor expressed in CHOK1 cells assessed as cAMP activity, EC50=31.21μM	19328683
HEK293	Function assay			Displacement of [3H]SR141716 from human recombinant CB1 receptor expressed in HEK293 cells, Ki=0.001995μM	19338356
HEK293	Function assay			Displacement of [3H]SR141716 from human recombinant CB2 receptor expressed in HEK293 cells, Ki=0.39811μM	19338356
CHOK1	Function assay		10 mins	Antagonist activity at human CB1 receptor expressed in CHOK1 cells assessed as inhibition of CP-55940-induced response after 10 mins by GTPgamma[35S] binding assay, Ki=0.0016μM	19351113
HEK293	Function assay			Displacement of [3H]rimonabant from human CB1 receptor expressed in HEK293 cells by liquid scintillation counting, Ki=0.0019μM	19520572
HEK293	Function assay			Displacement of [3H]CP-55940 from human recombinant CB1R expressed in HEK293 cells, IC50=0.0132μM	19530697
HEK293	Function assay			Inverse agonist activity at human recombinant CB1R expressed in HEK293 cells assessed as inhibition of CP-55940-stimulated Eu-GTP binding, EC50=0.0157μM	19530697
HEK293	Function assay			Displacement of [3H]CP-55940 from human recombinant CB2R expressed in HEK293 cells, IC50=1.6311μM	19530697
HEK293	Function assay	10 uM		Intrinsic activity at human recombinant CB1R expressed in HEK293 cells assessed as Eu-GTP binding at 10 uM relative to basal level	19530697
HEK	Function assay			Displacement of [3H]CP-55940 from human recombinant CB1 receptor expressed in HEK cells, Ki=0.012μM	19595596
HEK	Function assay			Displacement of [3H]CP-55940 from human recombinant CB2 receptor expressed in HEK cells, Ki=0.79μM	19595596
CHO-K1	Function assay			Antagonist activity at human CB1 receptor transfected in CHO-K1cells by GTPgamma[35S] binding assay, Ki=0.0016μM	19683918
CHO	Function assay			Binding affinity to human CB2 receptor expressed in CHO cells by luciferase reporter gene assay, IC50=0.0925μM	19850473
CHOK1	Function assay			Displacement of [3H]WIN-552122 from human CB2 receptor expressed in CHOK1 cells, IC50=1.76μM	19850473
CHO-K1	Function assay			Antagonist activity at human recombinant CB1 receptor expressed in CHO-K1 cells assessed as inhibition of CP-55940-stimulated GTPgammaS binding, IC50=0.0045μM	19954978
CHO-K1	Function assay			Inverse agonist activity at human CB1 receptor expressed in CHO-K1 cells by GTPgammaS binding assay, IC50=0.0029μM	20015647
CHO-K1	Function assay			Antagonist activity at human CB1 receptor expressed in CHO-K1 cells assessed as inhibition of CP-55940-induced GTPgammaS binding, IC50=0.0045μM	20015647
COS7	Function assay			Displacement of [3H]CP-55940 from human CB1 receptor expressed in COS7 cells, IC50=0.0051μM	20015647
CHO	Function assay			Inverse agonist activity at human recombinant CB1 receptor expressed in CHO cells by luciferase reporter gene assay, IC50=0.108μM	20045337
CHO	Function assay		60 mins	Inverse agonist activity at human cannabinoid CB1 receptor expressed in CHO cells assessed as inhibition of forskolin-stimulated cAMP accumulation after 60 mins, EC50=0.00011μM	20047779
CHO	Function assay		3 hrs	Displacement of [3H]CP-55940 from human recombinant cannabinoid CB1 receptor expressed in CHO cells after 3 hrs by liquid scintillation counting, Ki=0.00074μM	20047779
CHO	Function assay		10 mins	Antagonist activity at human cannabinoid CB1 receptor expressed in CHO cells coexpressing Galpha15/16 assessed as inhibition of CP-55940-induced Ca2+ release after 10 mins by micro plate reader, IC50=0.0032μM	20047779
CHO	Function assay		3 hrs	Displacement of [3H]CP-55940 from human recombinant cannabinoid CB2 receptor expressed in CHO cells after 3 hrs by liquid scintillation counting, Ki=0.126μM	20047779
CHO	Function assay			Antagonist activity at human CB1 receptor expressed in CHO cells assessed as inhibition of CP-55940-induced [3H]arachidonic acid release, Kd=0.002512μM	20363132
CHO	Function assay			Displacement of [3H]CP-55940 from human CB1 receptor expressed in CHO cells, Ki=0.025μM	20363132
CHO	Function assay			Displacement of [3H]CP-55940 from human CB2 receptor expressed in CHO cells, Ki=1.58μM	20363132
CHO-K1	Function assay		1 hr	Displacement of [3H]WIN-55212-2 from human CB2 receptor expressed in CHO-K1 cells after 1 hr by liquid scintillation counting, IC50=1.76μM	20673729
HEK	Function assay			Displacement of [3H]CP-55940 from human CB1 receptor expressed in HEK cells, Ki=0.012μM	20718492
HEK	Function assay			Displacement of [3H]CP-55940 from human CB2 receptor expressed in HEK cells, Ki=0.79μM	20718492
CHO	Function assay			Agonist activity at human CB1 receptor expressed in CHO cells co-expressing Galpha16 protein assessed as mobilization of intracellular calcium, Ke=0.0011μM	20845959
HEK293	Function assay			Displacement of [3H]SR141716 from human CB1 receptor expressed in HEK293 cells, Ki=0.00118μM	20845959
HEK293	Function assay			Displacement of [3H]CP55940 from human CB1 receptor expressed in HEK293 cells, Ki=0.00618μM	20845959
CHOK1	Function assay			Displacement of [3H]CP55940 from human CB2 receptor expressed in CHOK1 cells, Ki=0.313μM	20845959
HEK	Function assay			Displacement of [3H]CP-55,940 from recombinant human CB1 receptor transfected in HEK cells, Ki=0.012μM	20943290
HEK	Function assay			Displacement of [3H]CP-55,940 from recombinant human CB2 receptor transfected in HEK cells, Ki=0.79μM	20943290
CHO	Function assay			Displacement of [3H]SR141716A from human CB1 receptor expressed in CHO cells, Ki=0.0009333μM	21334892
Sf9	Function assay			Displacement of [3H]CP55940 from human recombinant CB2 receptor expressed in Sf9 cells, Ki=0.85114μM	21334892
CHO	Function assay			Antagonist activity at CB1 receptor transfected in CHO cells expressing apoaequorin as a reporter for G-protein-coupled receptor-mediated calcium signaling by bioluminescence assay, IC50=0.004μM	21376588
HEK293	Function assay			Noncompetitive inhibition of MRP1-mediated E2-17betaG transport in human MRP1 expressing HEK293 cells by Dixon plot, Ki=1.4μM	21511945
HEK293	Function assay			Noncompetitive inhibition of MRP4-mediated E2-17betaG transport in human MRP4 expressing HEK293 cells by Dixon plot, Ki=4μM	21511945
HEK293	Function assay			Induction of MRP2-mediated E2-17betaG transport in human MRP2 expressing HEK293 cells in presence of 2 uM E2-17betaG	21511945
HEK293	Function assay			Inhibition of MRP3-mediated E2-17betaG transport in human MRP3 expressing HEK293 cells in presence of 15 uM E2-17betaG	21511945
HEK293	Function assay			Inhibition of MRP1-mediated E2-17betaG transport in human MRP1 expressing HEK293 cells in presence of 0.6 to 5 uM E2-17betaG	21511945
HEK293	Function assay			Inhibition of MRP4-mediated E2-17betaG transport in human MRP4 expressing HEK293 cells in presence of 0.6 to 5 uM E2-17betaG	21511945
HEK	Function assay			Displacement of [3H]CP-55940 from human recombinant CB1 receptor expressed in HEK cells, Ki=0.012μM	21702498
HEK	Function assay			Displacement of [3H]CP-55940 from human recombinant CB2 receptor expressed in HEK cells, Ki=0.79μM	21702498
CHO	Function assay		1 hr	Displacement of [3H]CP55940 from human cannabinoid CB2 receptor expressed in CHO cells at pH 7.4 after 1 hr by liquid scintillation counting, IC50=1.98μM	21741835
HEK293	Function assay		5 mins	Inhibition of human ERG expressed in HEK293 cells assessed as inhibition of potassium channel current after 5 mins by patch clamp assay, IC50=2.79μM	21741835
CHO	Function assay		90 mins	Displacement of [3H]BMS-725519 from human CB1 receptor expressed in CHO cells after 90 mins by scintillation counting, Ki=0.00073μM	21962575
CHO-K1	Function assay			Antagonist activity at human CB1 receptor expressed in CHO-K1 cells co-expressing Galphaq16 assessed as inhibition of CP55940-induced intracellular calcium mobilization by fluorometry, Ke=0.0011μM	22372835
CHO-K1	Function assay			Displacement of [3H]CP55940 from human CB1 receptor expressed in CHO-K1 cells, Ki=0.0062μM	22372835
CHO-K1	Function assay			Displacement of [3H]CP55940 from CB2 receptor expressed in CHO-K1 cells, Ki=0.313μM	22372835
HEK	Function assay			Displacement of [3H]CP-55,940 from human recombinant CB1 receptor transfected in HEK cells, Ki=0.012μM	22548457
HEK	Function assay			Displacement of [3H]CP-55,940 from human recombinant CB2 receptor transfected in HEK cells, Ki=0.79μM	22548457
CHO	Function assay		2 hrs	Displacement of [3H]CP55,940 from human CB1 receptor expressed in CHO cells after 2 hrs by liquid scintillation counter, Ki=0.0126μM	22916707
CHO	Function assay		2 hrs	Displacement of [3H]CP55,940 from human CB2 receptor expressed in CHO cells after 2 hrs by liquid scintillation counter, Ki=0.9μM	22916707
CHO	Function assay			Inverse agonist activity against CB1 receptor expressed in human CHO cells assessed as effect on forskolin-stimulated cAMP level, IC50=0.051μM	22959249
CHO	Function assay		1 hr	Displacement of [3H]CP55940 from human CB1 receptor expressed in CHO cells incubated for 1 hr, Ki=0.0106μM	23072339
CHO	Function assay	> 0.1 nM	1 hr	Inverse agonist activity at human recombinant CB1 receptor transfected in CHO cells assessed as reduction of [35S]GTPgammaS binding at > 0.1 nM after 1 hr by liquid scintillation spectrometry	23357307
N1E-115	Function assay	1 uM	5 mins	Inverse agonist activity at CB1 receptor in mouse N1E-115 cells assessed as inhibition of WIN 55,212-2-induced ERK1/2 phosphorylation at 1 uM treated 5 mins prior to WIN 55,212-2 challenge by Western blot analysis	23357307
CHO	Function assay			Antagonist activity at human GPR18 transfected in CHO cells assessed as delta9-THC-induced beta-arrestin recruitment incubated 60 mins prior to delta9-THC addition by beta-arrestin translocation assay, IC50=10.1μM	23679955
HEK	Function assay		1 hr	Antagonist activity at human CB1 receptor overexpressed in HEK cells assessed as [35S]GTPgamma binding after 1 hr by liquid scintillation counting analysis, EC50=0.0015μM	24175572
CHOK1	Function assay		1 hr	Displacement of [3H]CP55940 from human CB1 receptor expressed in CHOK1 cells after 1 hr by liquid scintillation counting analysis, Ki=0.0059μM	24175572
CHO	Function assay		45 mins	Antagonist activity at human CB1 receptor stably expressed in CHO cells co-expressing co-expressing Ga15/16 assessed as calcium current after 45 mins by fluo-4 AM assay, IC50=0.013μM	24445310
CHO	Function assay		45 mins	Antagonist activity at CB2 receptor (unknown origin) stably expressed in CHO cells co-expressing co-expressing Ga15/16 assessed as calcium current after 45 mins by fluo-4 AM assay, IC50=9.8μM	24445310
CHO-K1	Function assay		10 mins	Antagonist activity at human CB1 receptor expressed in CHO-K1 cells assessed as inhibition of CP-55940-induced [35S]GTPgammaS binding incubated for 10 mins prior to CP-55940-challenge measured after 1 hr by beta counting, Ki=0.0016μM	24900484
HEK293	Function assay		60 mins	Displacement of [3H]SR141716A form human CB1 receptor expressed in HEK293 cells after 60 mins by beta counting, Ki=0.0018μM	24900484
CHO-K1	Function assay		60 mins	Displacement of [3H]CP-55940 from human CB2 receptor expressed in CHO-K1 cells after 60 mins by beta counting, Ki=0.522μM	24900484
CHO	Function assay		2 hrs	Displacement of [3H]CP55,940 from recombinant human CB1 receptor expressed in CHO cells after 2 hrs by liquid scintillation counting, Ki=0.0126μM	24900561
CHO	Function assay		2 hrs	Displacement of [3H]CP55,940 from recombinant human CB2 receptor expressed in CHO cells after 2 hrs by liquid scintillation counting, Ki=0.9μM	24900561
CHO	Function assay		90 mins	Agonist activity at GPR55 (unknown origin) expressed in CHO cells assessed as inhibition of LPI-induced beta-arrestin translocation after 90 mins by luminescence assay, EC50=2.01μM	24900561
RD-HGA16	Function assay			Antagonist activity at CB1-OX1 heterodimer (unknown origin) expressed in RD-HGA16 cells assessed as inhibition of orexin A-induced calcium mobilization by fluorometric imaging plate reader analysis, Ke=0.001μM	24944734
RD-HGA16	Function assay			Antagonist activity at CB1 receptor (unknown origin) expressed in RD-HGA16 cells assessed as inhibition of CP55940-induced calcium mobilization by fluorometric imaging plate reader analysis, Ke=0.0011μM	24944734
Sf9	Function assay		20 mins	Inverse agonist activity at human CB1 receptor expressed in Sf9 cells coexpressing Gbeta1gamma2 and RSG4 assessed as degradation of [gamma-33P]GTP after 20 mins by steady-state GTPase assay, EC50=0.05μM	25096297
Sf9	Function assay		20 mins	Inverse agonist activity at human CB1 receptor expressed in Sf9 cells coexpressing Gbeta1gamma2 and RSG4 assessed as degradation of [gamma-33P]GTP after 20 mins by steady-state GTPase assay, EC50=0.05012μM	25096297
CHO	Function assay			Antagonist activity against CB1R (unknown origin) CHO cells stably expressing Galpha16 assessed as inhibition of CP55940-induced increase in intracellular calcium level pre-treated 10 mins before CP55940 stimulation by microplate reader based assay, IC50=0.0135μM	26151231
CHO	Function assay			Antagonist activity against CB2R (unknown origin) CHO cells stably expressing Galpha16 assessed as inhibition of CP55940-induced increase in intracellular calcium level pre-treated 10 mins before CP55940 stimulation by microplate reader based assay, IC50=9.1μM	26151231
HEK293	Function assay			Immediate antagonist/Inverse agonist activity at hemagglutinin-tagged human CB1 receptor expressed in HEK293 cells assessed as reversal of 1 uM CP55,940-induced inhibition of 5 uM forskolin-induced cAMP accumulation by kinetic cAMP assay	26203658
HEK293	Function assay		90 mins	Displacement of [3H]-CP-55940 from human recombinant CB1 receptor expressed in HEK293 cells after 90 mins by Competition binding assay, Kieq=0.012μM	26756097
HEK293	Function assay		90 mins	Displacement of [3H]-CP-55940 from human recombinant CB2 receptor expressed in HEK293 cells after 90 mins by Competition binding assay, Kieq=0.79μM	26756097
CHO-K1	Function assay			Antagonist activity at human CB1 receptor expressed in CHO-K1 cells assessed as inhibition of CP55940-induced intracellular calcium mobilization by Calcein-4 AM-staining based FLIPR assay, Ke=0.0011μM	26827137
CHO	Function assay		90 secs	Inverse agonist activity at human CB1 receptor expressed in CHO cells assessed as increase in intracellular calcium mobilization after 90 secs by Calcein-4 AM-staining based FLIPR assay, EC50=0.005μM	26827137
SJ-GBM2	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SJ-GBM2 cells	29435139
A673	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for A673 cells	29435139
SK-N-MC	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-MC cells	29435139
BT-37	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-37 cells	29435139
SK-N-SH	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for SK-N-SH cells	29435139
NB1643	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for NB1643 cells	29435139
LAN-5	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for LAN-5 cells	29435139
BT-12	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for BT-12 cells	29435139
OHS-50	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for OHS-50 cells	29435139
RD	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Primary screen for RD cells	29435139
A673	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for A673 cells)	29435139
SK-N-MC	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for SK-N-MC cells	29435139
DAOY	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for DAOY cells	29435139
TC32	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for TC32 cells	29435139
U-2 OS	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for U-2 OS cells	29435139
Rh41	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Rh41 cells	29435139
Saos-2	qHTS assay			qHTS of pediatric cancer cell lines to identify multiple opportunities for drug repurposing: Confirmatory screen for Saos-2 cells	29435139
CHOK1	Function assay		90 mins	Inverse agonist activity at C-terminally prolink-tagged mouse CB2 receptor expressed in CHOK1 cells harboring beta-galactosidase enzyme fused beta-arrestin assessed as increase in beta-arrestin recruitment after 90 mins by chemiluminescent assay, EC50=0.015μM	29939744
HEK293	Function assay			Antagonist activity at human CB1 receptor expressed in HEK293 cells by GTPgammaS binding assay, Ke=0.0002μM	30077609
HEK293	Function assay		90 secs	Inverse agonist activity at human CB1 receptor expressed in HEK293 cells co-expressing Galphaq16 assessed as inhibition of calcium mobilization after 90 secs by calcein-4 AAM dye-based FLIPR assay, EC50=0.586μM	30077609
HEK293	Function assay		30 mins	Inverse agonist activity at human CB1 receptor expressed in HEK293 cells assessed as inhibition of forskolin-induced cAMP accumulation after 30 mins by HTRF assay, EC50=0.0041μM	30339387
CHO	Function assay			Displacement of [3H]-CP55940 from human recombinant cannabinoid CB1 receptor expressed in CHO cells by radioligand binding assay, Ki=0.143μM	31609608
CHO	Function assay			Agonist activity at human GPR55 expressed in CHO cells assessed as induction of LPI-induced beta-arrestin recruitment by beta-galactosidase enzyme fragment complementation method, EC50=2.01μM	ChEMBL
CHO	Function assay			Agonist activity at human GPR18 expressed in CHO cells assessed as induction of beta-arrestin recruitment by beta-galactosidase enzyme fragment complementation method, EC50=10.1μM	ChEMBL
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Información química, almacenamiento y estabilidad

Peso molecular	463.79	Fórmula	C₂₂H₂₁Cl₃N₄O	Almacenamiento (Desde la fecha de recepción)	3 años-20°Cpolvo
Nº CAS	168273-06-1	Descargar SDF		Almacenamiento de soluciones madre	1 año-80°Cen disolvente 1 mes-20°Cen disolvente
Sinónimos	N/A			Smiles	CC1=C(N(N=C1C(=O)NN2CCCCC2)C3=C(C=C(C=C3)Cl)Cl)C4=CC=C(C=C4)Cl

Solubilidad

In vitro
Lote:

DMSO : 92 mg/mL (198.36 mM)
(El DMSO contaminado con humedad puede reducir la solubilidad. Usar DMSO fresco y anhidro.)

Ethanol : 50 mg/mL

Water : Insoluble

Calculadora de Molaridad

Masa	Concentración	Volumen	Peso molecular
=	×	×

Calculadora de Dilución Calculadora de Peso Molecular

In vivo Lote:
Homogeneous suspension	CMC-NA	≥5mg/ml	Taking the 1 mL working solution as an example, add 5 mg of this product to 1 ml of CMC-Na solution, mix evenly to obtain a homogeneous suspension with a final concentration of 5 mg/ml.
Homogeneous suspension	CMC-NA	≥5mg/ml	Taking the 1 mL working solution as an example, add 5 mg of this product to 1 ml of CMC-Na solution, mix evenly to obtain a homogeneous suspension with a final concentration of 5 mg/ml.
Clear solution	5%DMSO 1 40%PEG300 2 5%Tween80 3 ddH2O Validado por los laboratorios Selleck. Si necesita ajustes en esta formulación, contacte con nuestro equipo de ventas para pruebas personalizadas.	5.000mg/ml (10.78mM)	Taking the 1 mL working solution as an example, add 50 μL of 100 mg/ml clarified DMSO stock solution to 400 μL of PEG300, mix evenly to clarify it; add 50 μL of Tween80 to the above system, mix evenly to make it clear; then continue to add 500 μL of ddH2O to adjust the volume to 1 mL. The mixed solution should be used immediately for optimal results.
Homogeneous suspension	CMC-NA	≥5mg/ml	Taking the 1 mL working solution as an example, add 5 mg of this product to 1 ml of CMC-Na solution, mix evenly to obtain a homogeneous suspension with a final concentration of 5 mg/ml.
Homogeneous suspension	CMC-NA	≥5mg/ml	Taking the 1 mL working solution as an example, add 5 mg of this product to 1 ml of CMC-Na solution, mix evenly to obtain a homogeneous suspension with a final concentration of 5 mg/ml.

Calculadora de formulación in vivo (Solución clara)

Paso 1: Introduzca la información a continuación (Recomendado: Un animal adicional para tener en cuenta la pérdida durante el experimento)

Dosis: mg/kg Peso promedio de los animales: g Volumen de dosificación por animal:μL Número de animales:

Paso 2: Introduzca la formulación in vivo (Esto es solo la calculadora, no la formulación. Por favor, contáctenos primero si no hay una formulación in vivo en la sección de Solubilidad.)

% DMSO + % + % Tween 80 + % ddH₂O

%DMSO+ %

Resultados del cálculo:

Concentración de trabajo: mg/ml;

Método para preparar el líquido maestro de DMSO: mg fármaco predissuelto en μL DMSO ( Concentración del líquido maestro mg/mL, Por favor, contáctenos primero si la concentración excede la solubilidad del DMSO del lote del fármaco. )

Método para preparar la formulación in vivo: Tomar μL DMSO líquido maestro, luego añadirμL PEG300, mezclar y clarificar, luego añadirμL Tween 80, mezclar y clarificar, luego añadir μL ddH₂O, mezclar y clarificar.

Método para preparar la formulación in vivo: Tomar μL DMSO líquido maestro, luego añadir μL Aceite de maíz, mezclar y clarificar.

Nota: 1. Por favor, asegúrese de que el líquido esté claro antes de añadir el siguiente disolvente.
2. Asegúrese de añadir el (los) disolvente(s) en orden. Debe asegurarse de que la solución obtenida, en la adición anterior, sea una solución clara antes de proceder a añadir el siguiente disolvente. Se pueden utilizar métodos físicos como el vórtice, el ultrasonido o el baño de agua caliente para ayudar a la disolución.

Mecanismo de acción

Características	Efficacious to induce weight reduction and improvements in cardiometabolic risk factors, however was withdrawn in 2009 due to severe depressive disorder and anxiety.
Targets/IC₅₀/Ki	ACAT1 ACAT2 MmpL3 hCB1 (Cell-free assay) 13.6 nM hCB2 (Cell-free assay) 1.64 μM
In vitro	Rimonabant (SR141716) reduce de forma dosis-dependiente la actividad de la ACAT en macrófagos Raw264.7 con una IC50 de 2,9 μM y en macrófagos peritoneales aislados. Inhibe la actividad de la ACAT en células CHO-ACAT1 y CHO-ACAT2 intactas y en ensayos libres de células con una eficiencia aproximadamente igual, con una IC50 de 1,5 μM y 2,2 μM para CHO-ACAT1 y CHO-ACAT2, respectivamente. De acuerdo con la inhibición de la ACAT, este tratamiento con el compuesto bloquea los procesos dependientes de la ACAT en macrófagos, la apoptosis inducida por oxisterol y la formación de células espumosas inducida por LDL acetilado. Antagoniza los efectos inhibidores de los agonistas del Cannabinoid Receptor tanto en las contracciones del conducto deferente de ratón como en la actividad de la adenilil ciclasa en membranas de cerebro de rata de forma concentración-dependiente. El compuesto reduce significativamente el crecimiento celular e induce la muerte celular de células de cáncer colorrectal humano (DLD-1, CaCo-2 y SW620). Es capaz de alterar la distribución del ciclo celular en todas las líneas celulares probadas. En particular, Rimonabant produce una detención del ciclo celular en G2/M en células DLD-1 sin inducir apoptosis o necrosis.
Ensayo de quinasa	Ensayo de unión a radioligandos
Ensayo de quinasa	Se purifican las células HEK 293 transfectadas de forma estable con CB1 y CB2 humanos y la membrana celular. Se incuban 0,2-8 μg de la membrana purificada con 0,75 nM de [³H] CP55,940 y Rimonabant (SR141716) en el tampón de incubación (50 mM Tris-HCl, 5 mM MgCl₂, 1 mM EDTA, 0,3% BSA, pH 7,4). La unión no específica se define en presencia de 1 μM de CP55,940. Las reacciones se incuban durante una hora y media a 30 °C en Multiscreen. Las reacciones se terminan mediante filtración múltiple y se lavan cuatro veces con tampón de lavado helado (50 mM Tris, pH 7,4, 0,25% BSA). La radiactividad unida a los filtros se mide mediante Topcount. La IC50 se determina como la concentración de este compuesto necesaria para inhibir el 50% de la unión de [³H] CP55,940 y se calcula mediante regresión no lineal.
In vivo	Rimonabant (SR141716) se administra por vía intraperitoneal u oral y antagoniza potente y dosis-dependientemente los efectos farmacológicos y conductuales clásicos de los agonistas del Cannabinoid Receptor. En el modelo de ratón de carcinogénesis de colon inducida por azoximetano, disminuyó significativamente la formación de focos de criptas aberrantes (ACF), que precede al cáncer colorrectal. Este compuesto (10 mg/kg por sonda) se administra durante 2 semanas a ratas Zucker obesas macho de 3 meses como modelo de intolerancia a la glucosa y durante 10 semanas a ratas Zucker obesas macho de 6 meses como modelo de síndrome metabólico. Los niveles séricos de RANTES (Regulated upon Activation, Normal T cell Expressed, and Secreted) y MCP-1 (proteína quimioatrayente de monocitos-1) aumentan en ratas Zucker obesas en comparación con las delgadas y se reducen significativamente con el tratamiento a largo plazo con este, lo que ralentiza el aumento de peso en ratas con síndrome metabólico. Los neutrófilos y monocitos aumentan significativamente en ratas Zucker obesas jóvenes y viejas en comparación con las delgadas y se reducen con este compuesto. El fibrinógeno unido a plaquetas se mejora significativamente en ratas Zucker obesas en comparación con las delgadas de ambas edades, y se reduce con este. Las plaquetas de ratas obesas son más sensibles a la agregación inducida por trombina y a la adhesión al fibrinógeno, los cuales son atenuados por la terapia con Rimonabant.
Referencias	[1] https://pubmed.ncbi.nlm.nih.gov/18802648/ [2] https://pubmed.ncbi.nlm.nih.gov/20609360/ [3] https://pubmed.ncbi.nlm.nih.gov/8070571/ [4] https://pubmed.ncbi.nlm.nih.gov/19479993/ [5] https://pubmed.ncbi.nlm.nih.gov/18469848/ [6] https://pubmed.ncbi.nlm.nih.gov/17213845/ [7] https://pubmed.ncbi.nlm.nih.gov/30682372/

Aplicaciones

Métodos	Biomarcadores	Imágenes	PMID
Western blot	CD44 / Lgr5 / CD133 / EpCAM β-catenin p-LRP6 / LRP6 / Lgr5		29354056
Immunofluorescence	β-catenin Lgr5		29354056

Información del ensayo clínico

(datos de https://clinicaltrials.gov, actualizado el 2024-05-22)

Número NCT	Reclutamiento	Condiciones	Patrocinador/Colaboradores	Fecha de inicio	Fases
NCT00750347	Completed	Pain	University Hospital Clermont-Ferrand	September 2008	Phase 1
NCT00656487	Completed	Cannabis Dependence\|Cannabis Withdrawal	The Scripps Research Institute\|National Institute on Drug Abuse (NIDA)	April 30 2008	Phase 2
NCT00546325	Completed	Diabetes Mellitus Type 2	Sanofi	October 2007	Phase 3
NCT00525681	Completed	Renal Transplantation	University of Oslo School of Pharmacy	September 2007	Phase 4
NCT00584389	Terminated	Obesity	University of Surrey\|European Foundation for the Study of Diabetes\|Royal Surrey County Hospital NHS Foundation Trust	July 2007	Phase 4
NCT01041170	Completed	Cannabis\|Dependence	National Institute on Drug Abuse (NIDA)\|National Institutes of Health Clinical Center (CC)	April 16 2006	Phase 1

Soporte técnico

Instrucciones de manipulación

Tel: +1-832-582-8158 Ext:3

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