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CHEMBRDG-BB 5280909, also known as ML-354, is an indole-based, proteinase-activated receptor 4 (PAR4) antagonist with an IC50 of 140 nM. It demonstrates 71-fold selectivity for PAR4 over PAR1 in isolated human platelets.

89159-60-4

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89159-60-4 Usage

Uses

Used in Pharmaceutical Industry:
CHEMBRDG-BB 5280909 is used as a selective protease activated receptor 4 (PAR-4) antagonist for its antithrombotic effects, potentially offering a targeted approach to treating conditions related to blood clotting and vascular health.

Biochem/physiol Actions

ML354 is a potent and selective PAR4 (protease activated receptor-4) antagonist.

IC 50

140 nm

references

[1]. wen, w., young, s., duvernay, m., schulte, m., nance, k., & melancon, b. et al. substituted indoles as selective protease activated receptor 4 (par-4) antagonists: discovery and sar of ml354. bioorganic & medicinal chemistry letters. 2014; 24(19): 4708-4713.

Check Digit Verification of cas no

The CAS Registry Mumber 89159-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,1,5 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 89159-60:
(7*8)+(6*9)+(5*1)+(4*5)+(3*9)+(2*6)+(1*0)=174
174 % 10 = 4
So 89159-60-4 is a valid CAS Registry Number.
InChI:InChI=1/C16H14N2O3/c1-17-14-8-7-12(18(20)21)9-13(14)16(15(17)10-19)11-5-3-2-4-6-11/h2-9,19H,10H2,1H3

89159-60-4 Well-known Company Product Price

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  • Sigma

  • (SML1439)  ML354  ≥98% (HPLC)

  • 89159-60-4

  • SML1439-5MG

  • 858.78CNY

  • Detail
  • Sigma

  • (SML1439)  ML354  ≥98% (HPLC)

  • 89159-60-4

  • SML1439-25MG

  • 3,473.73CNY

  • Detail

89159-60-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name (1-methyl-5-nitro-3-phenylindol-2-yl)methanol

1.2 Other means of identification

Product number -
Other names 1-methyl-2-hydroxymethyl-3-phenyl-5-nitroindole

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:89159-60-4 SDS

89159-60-4Relevant academic research and scientific papers

A NEW APPROACH TO THE SYNTHESIS OF 2-AMINOMETHYL-3-PHENYL-5-NITROINDOLE

Krichevskii, E. S.,Romanova, O. B.,Grinev, A. N.

, p. 1302 - 1305 (2007/10/02)

Bromination of 2-methyl-3-phenyl-5-nitroindoles has given previously unknown 2-bromoethyl-3-phenyl-5-nitroindoles, which were converted by the Delepine reaction into 2-aminomethyl-3-phenyl-5-nitroindoles.One of these (1-methyl-2-aminomethyl-3-phenyl-5-nitroindole) was also obtained by reductive amination of 1-methyl-2-formyl-3-phenyl-5-nitroindole by the Leuckart-Wallach reaction.

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