CMPD101

CAS
865608-11-3
Catalog Number
ACM865608113
Category
Inhibitors
Molecular Weight
466.47
Molecular Formula
C24H21F3N6O

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Specification

Description
CMPD101 is a novel, potent and selective G-protein coupled receptor kinase 2 and 3 (GRK2/GRK3) inhibitor (IC50 values are 35 and 32 nM at GRK2 and GRK3 respectively). CMPD101 exhibits selectivity for GRK2/3 over GRK1/5 and reduces DAMGO-induced desensitization and internalization of μ-opioid receptors. CMPD101 has been shown to potentiate phosphatidylinositol 4,5-bisphosphate (PIP2) depletion and slow agonist-induced desensitization of protease-activated receptor 2 (PAR2).
Synonyms
CMPD101; CMPD 101; CMPD-101; Takeda101; Takeda-101; Takeda 101
IUPAC Name
3-[[[4-Methyl-5-(4-pyridinyl)-4H-1,2,4-triazol-3-yl]methyl]amino]-N-[[2-(trifluoromethyl)phenyl]methyl]benzamide
Canonical SMILES
O=C(NCC1=CC=CC=C1C(F)(F)F)C2=CC=CC(NCC3=NN=C(C4=CC=NC=C4)N3C)=C2
InChI
InChI=1S/C24H21F3N6O/c1-33-21(31-32-22(33)16-9-11-28-12-10-16)15-29-19-7-4-6-17(13-19)23(34)30-14-18-5-2-3-8-20(18)24(25,26)27/h2-13,29H,14-15H2,1H3,(H,30,34)
InChI Key
WFOVEDJTASPCIR-UHFFFAOYSA-N
Solubility
Soluble in DMSO, not in water
Appearance
Solid powder
Shelf Life
>2 years if stored properly
Storage
Dry, dark and at 0-4 °C for short term (days to weeks) or -20 °C for long term (months to years).
Biological Target
CMPD101 is a small-molecule inhibitor of GRK2/3 with IC50 of 18 nM and 5.4 nM, respectively.
Drug Formulation
This drug may be formulated in DMSO
Elemental Analysis
C, 61.80; H, 4.54; F, 12.22; N, 18.02; O, 3.43
Exact Mass
466.17289
HS Tariff Code
2934.99.9001
In Vitro Activity
In conclusion, CMPD101 inhibits adrenergic, neurogenic, and non-adrenergic smooth muscle contractions in the human prostate.
In Vivo Activity
TBD
Shipping
Shipped under ambient temperature as non-hazardous chemical. This product is stable enough for a few weeks during ordinary shipping and time spent in Customs.
Stock Solution Storage
0-4 °C for short term (days to weeks), or -20 °C for long term (months).
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