WAY-658513
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    WARNING: This product is for research use only, not for human or veterinary use.

Hodoodo CAT#: H556209

CAS#: 692870-25-0

Description: WAY-658513 is a multiple kinase inhbitor. WAY658513 was shown to inhibit ROCK I, ERK2, GSK3, and PKA with Ki <1 μM. WAY-658513 was first reported in patent WO2004041813


Chemical Structure

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WAY-658513
CAS# 692870-25-0

Theoretical Analysis

Hodoodo Cat#: H556209
Name: WAY-658513
CAS#: 692870-25-0
Chemical Formula: C16H11ClFN3OS
Exact Mass: 347.03
Molecular Weight: 347.792
Elemental Analysis: C, 55.26; H, 3.19; Cl, 10.19; F, 5.46; N, 12.08; O, 4.60; S, 9.22

Price and Availability

Size Price Availability Quantity
200mg USD 1650 2 Weeks
1g USD 4250 2 Weeks
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Synonym: WAY-658513; WAY 658513; WAY658513;

IUPAC/Chemical Name: Benzeneacetamide, 2-chloro-6-fluoro-N-[4-(4-pyridinyl)-2-thiazolyl]-

InChi Key: BPGUVXHQHDKSTA-UHFFFAOYSA-N

InChi Code: InChI=1S/C16H11ClFN3OS/c17-12-2-1-3-13(18)11(12)8-15(22)21-16-20-14(9-23-16)10-4-6-19-7-5-10/h1-7,9H,8H2,(H,20,21,22)

SMILES Code: O=C(NC1=NC(C2=CC=NC=C2)=CS1)CC3=C(F)C=CC=C3Cl

Appearance: To be determined

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: To be determined

Shelf Life: >2 years if stored properly

Drug Formulation: To be determined

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 347.79 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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Preparation of thienyl- and thiazolecarboxamides as inhibitors of ROCK, ERK, GSK, and AGC protein kinases
By: Cao, Jingrong; Gao, Huai; Green, Jeremy; Marhefka, Craig
World Intellectual Property Organization, WO2004041813 A1 2004-05-21 | Language: English, Database: CAplus