Welcome to LookChem.com Sign In|Join Free

CAS

  • or

165669-36-3

Post Buying Request

165669-36-3 Suppliers

Recommended suppliersmore

  • Product
  • FOB Price
  • Min.Order
  • Supply Ability
  • Supplier
  • Contact Supplier

165669-36-3 Usage

General Description

1H-Pyrrolo[2,3-c]pyridin-7-amine(9CI) is a chemical compound with the molecular formula C9H8N2. It is a heterocyclic compound that contains a pyrrolopyridine ring system. This chemical is also known as aminomethylpyridine and is commonly used in the synthesis of various pharmaceutical compounds and organic materials. It has potential applications in the field of medicinal chemistry and drug discovery due to its ability to modify and interact with biological systems. The compound has attracted interest in recent years for its potential as a building block for the construction of various bioactive molecules and pharmaceutical agents. Additionally, 1H-Pyrrolo[2,3-c]pyridin-7-amine(9CI) has also been studied for its potential antitumor and antimicrobial activities. Overall, this compound is a valuable and versatile building block with potential applications in the fields of organic and medicinal chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 165669-36-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,5,6,6 and 9 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 165669-36:
(8*1)+(7*6)+(6*5)+(5*6)+(4*6)+(3*9)+(2*3)+(1*6)=173
173 % 10 = 3
So 165669-36-3 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3/c8-7-6-5(1-3-9-6)2-4-10-7/h1-4,9H,(H2,8,10)

165669-36-3SDS

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 1H-pyrrolo[2,3-c]pyridin-7-amine

1.2 Other means of identification

Product number -
Other names 7-Amino-6-azaindole

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:165669-36-3 SDS

165669-36-3Relevant articles and documents

Selective Inhibitors of Helicobacter pylori Methylthioadenosine Nucleosidase and Human Methylthioadenosine Phosphorylase

Harijan, Rajesh K.,Hoff, Oskar,Ducati, Rodrigo G.,Firestone, Ross S.,Hirsch, Brett M.,Evans, Gary B.,Schramm, Vern L.,Tyler, Peter C.

, p. 3286 - 3296 (2019)

Bacterial 5′-methylthioadenosine/S-adenosylhomocysteine nucleosidase (MTAN) hydrolyzes adenine from its substrates to form S-methyl-5-thioribose and S-ribosyl-l-homocysteine. MTANs are involved in quorum sensing, menaquinone synthesis, and 5′-methylthioadenosine recycling to S-adenosylmethionine. Helicobacter pylori uses MTAN in its unusual menaquinone pathway, making H. pylori MTAN a target for antibiotic development. Human 5′-methylthioadenosine phosphorylase (MTAP), a reported anticancer target, catalyzes phosphorolysis of 5′-methylthioadenosine to salvage S-adenosylmethionine. Transition-state analogues designed for HpMTAN and MTAP show significant overlap in specificity. Fifteen unique transition-state analogues are described here and are used to explore inhibitor specificity. Several analogues of HpMTAN bind in the picomolar range while inhibiting human MTAP with orders of magnitude weaker affinity. Structural analysis of HpMTAN shows inhibitors extending through a hydrophobic channel to the protein surface. The more enclosed catalytic sites of human MTAP require the inhibitors to adopt a folded structure, displacing the phosphate nucleophile from the catalytic site.

Integrin expression inhibitors

-

, (2008/06/13)

The present invention provides an integrin expression inhibitor, and an agent for treating arterial sclerosis, psoriasis, cancer, retinal angiogenesis, diabetic retinopathy or inflammatory diseases, an anticoagulant, or a cancer metastasis suppressor on the basis of an integrin inhibitory action. Namely, it provides an integrin expression inhibitor comprising, as an active ingredient, a sulfonamide compound represented by the following formula (I), a pharmacologically acceptable salt thereof or a hydrate of them. In the formula, B means a C6-C10 aryl ring or 6- to 10-membered heteroaryl ring which may have a substituent and in which a part of the ring may be saturated; K means a single bond, —CH═CH— or —(CR4bR5b)mb— (wherein R4b and R5b are the same as or different from each other and each means hydrogen atom or a C1-C4 alkyl group; and mb means an integer of 1 or 2); R1 means hydrogen atom or a C1-C6 alkyl group; Z means a single bond or —CO—NH—; and R means a C6-C10 aryl ring or 6- to 10-membered heteroaryl ring which may have a substituent and in which a part of the ring may be saturated, respectively.

Post a RFQ

Enter 15 to 2000 letters.Word count: 0 letters

Attach files(File Format: Jpeg, Jpg, Gif, Png, PDF, PPT, Zip, Rar,Word or Excel Maximum File Size: 3MB)

1

What can I do for you?
Get Best Price

Get Best Price for 165669-36-3