JWH 200-d5

JWH 200-d5 Suppliers list
Company Name: Cayman Chemical Company  
Tel: (800) 364-9897
Email: cayman@caymanchem.com
Products Intro: Product Name:JWH 200-d5
CAS:1651833-51-0
Package:>=99% deuterated product Remarks:10903
Company Name: Absin Bioscience Inc.  
Tel: 021-38015121
Email: chenjw@absin.cn
Products Intro: Product Name:JWH 200-d5 (exempt preparation)
CAS:1651833-51-0
Company Name: Shanghai Hao Zhun Biological Technology Co., Ltd.  
Tel: 15800340161
Email: info@zzsrm.com
Products Intro: Product Name:JWH 200-d5 (exempt preparation)
CAS:1651833-51-0
Purity:99% deuterated forms (d1-d5)
Company Name: Shanghai Haoran Biotechnology Co., Ltd.  
Tel: 021-54046791
Email: 470003480@QQ.COM
Products Intro: Product Name:JWH 200-d5 (exempt preparation)
CAS:1651833-51-0
Company Name: Shanghai Jijin Chemical Technology Co., Ltd.  
Tel: 400-002-6926 15900443528
Email: jijinhuaxue@sina.com
Products Intro: Product Name:JWH 200-d5 (exempt preparation)
CAS:1651833-51-0
JWH 200-d5 Basic information
Product Name:JWH 200-d5
Synonyms:JWH 200-d5;JWH 200-d5 (exempt preparation)
CAS:1651833-51-0
MF:C25H24N2O2
MW:384.48
EINECS:
Product Categories:
Mol File:1651833-51-0.mol
JWH 200-d5 Structure
JWH 200-d5 Chemical Properties
solubility Acetonitrile: 14 mg/ml; DMF: 25 mg/ml; DMF:PBS(pH 7.2)(1:6): 0.1 mg/ml; DMSO: 20 mg/ml; Methanol: 2 mg/ml; Methyl Acetate: 5 mg/ml
form A crystalline solid
Safety Information
MSDS Information
JWH 200-d5 Usage And Synthesis
DescriptionJWH 200-d5 contains five deuterium atoms at the 2', 4' ,5', 6', and 7' positions. It is intended for use as an internal standard for the quantification of JWH 200 by GC- or LC-mass spectrometry. JWH 200 is an aminoalkylindole that acts as a cannabinoid (CB) receptor ligand. It binds to the CB1 receptor with high-affinity (IC50 = 7.8-42 nM).1,2 The effects of JWH 200 in locomotor activity, tail-flick latency, hypothermia, and ring-immobility tests are comparable or superior to Δ9-THC or WIN 55,212.3 It potently inhibits the contraction of electrically-stimulated mouse vas deferens (IC50 = 3.7-6.0 nM).4,5
References1. Eissenstat, M.A., Bell, M.R., D'Ambra, T.E., et al. Aminoalkylindoles: Structure-activity relationships of novel cannabinoid mimetics J. Med. Chem. 38,3094-3105(1995).
2. Huffman, J.W., Mabon, R., Wu, M.J., et al. 3-indolyl-1-naphthylmethanes: New cannabimimetic indoles provide evidence for aromatic stacking interactions with the CB1 cannabinoid receptor Bioorgan. Med. Chem. 11(4),539-549(2003).
3. Compton, D.R., Gold, L.H., Ward, S.J., et al. Aminoalkylindole analogs: Cannabimimetic activity of a class of compounds structurally distinct from D 9-tetrahydrocannabinol J. Pharmacol. Exp. Ther. 263(3),1118-1126(1992).
4. Pacheco, M., Childers, S.R., Arnold, R., et al. Aminoalkylindoles: Actions on specific G-protein-linked receptors J. Pharmacol. Exp. Ther. 257(1),170-183(1991).
5. Bell, M.R., D'Ambra, T.E., Kumar, V., et al. Antinociceptive (aminoalkyl) indoles J. Med. Chem. 34,1099-1110(1991).
JWH 200-d5 Preparation Products And Raw materials
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