WAY 629 hydrochloride
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Hodoodo CAT#: H574440

CAS#: 57756-44-2

Description: WAY 629 hydrochloride is a 5-HT2C agonist that stimulates intracellular Ca2+ mobilization in CHO cells expressing human 5-HT2C receptors.


Chemical Structure

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WAY 629 hydrochloride
CAS# 57756-44-2

Theoretical Analysis

Hodoodo Cat#: H574440
Name: WAY 629 hydrochloride
CAS#: 57756-44-2
Chemical Formula: C15H19ClN2
Exact Mass: 262.12
Molecular Weight: 262.780
Elemental Analysis: C, 68.56; H, 7.29; Cl, 13.49; N, 10.66

Price and Availability

Size Price Availability Quantity
10mg USD 330 2 Weeks
50mg USD 1060 2 Weeks
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Synonym: WAY 629 hydrochloride, WAY 629 HCl

IUPAC/Chemical Name: 1,2,3,4,8,9,10,11-Octahydro[1,4]diazepino[6,7,1-jk]carbazole hydrochloride

InChi Key: PZXUJERSOFOWES-UHFFFAOYSA-N

InChi Code: InChI=1S/C15H18N2.ClH/c1-2-7-14-12(5-1)13-6-3-4-11-10-16-8-9-17(14)15(11)13;/h3-4,6,16H,1-2,5,7-10H2;1H

SMILES Code: [H]Cl.N1(CCNC2)C3=C(C4=C1C2=CC=C4)CCCC3

Appearance: Solid powder

Purity: >98% (or refer to the Certificate of Analysis)

Shipping Condition: 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.

Storage Condition: Dry, dark and at 0 - 4 C for short term (days to weeks) or -20 C for long term (months to years).

Solubility: Soluble in DMSO

Shelf Life: >3 years if stored properly

Drug Formulation: This drug may be formulated in DMSO

Stock Solution Storage: 0 - 4 C for short term (days to weeks), or -20 C for long term (months).

HS Tariff Code: 2934.99.9001

More Info:

Biological target:
In vitro activity:
In vivo activity:

Preparing Stock Solutions

The following data is based on the product molecular weight 262.78 Batch specific molecular weights may vary from batch to batch due to the degree of hydration, which will affect the solvent volumes required to prepare stock solutions.

Recalculate based on batch purity %
Concentration / Solvent Volume / Mass 1 mg 5 mg 10 mg
1 mM 1.15 mL 5.76 mL 11.51 mL
5 mM 0.23 mL 1.15 mL 2.3 mL
10 mM 0.12 mL 0.58 mL 1.15 mL
50 mM 0.02 mL 0.12 mL 0.23 mL
Formulation protocol:
In vitro protocol:
In vivo protocol:

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1. Sabb et al (2004) Cycloalkyl[b][1,4]benzodiazepinoindoles are agonists at the human 5-HT2C receptor. Bioorg.Med.Chem.Lett. 14 2603 PMID: 15109661

2. Dunlop et al (2004) Identification of cycloalkyl[b][1,4]benzodiazepinoindoles as novel 5-HT2C receptor agonists. Fund.Clin.Pharmacol. 18 145