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SNAP

CAS No.
79032-48-7
Chemical Name:
SNAP
Synonyms
SNAP;SNAP(D);S-Nitroso-acetyl penicillamine;S-NITROSO-N-ACETYLPENICILLAMINE;N-ACETYL-3-(NITROSOTHIO)-D-VALINE;N-Acetyl-S-nitroso-D-penicillaMine;S-NITRO-N-ACETYL-D,L-PENACILLAMINE;S-nitroso-N-acetyl-D-penicillamine;D-Valine, N-acetyl-3-(nitrosothio)-;S-Nitroso-N-acetyl-D-b,b-dimethylcysteine
CBNumber:
CB5736261
Molecular Formula:
C7H12N2O4S
Molecular Weight:
220.25
MDL Number:
MFCD00153852
MOL File:
79032-48-7.mol
Last updated:2023-06-30 15:45:59

SNAP Properties

Density 1.36±0.1 g/cm3(Predicted)
storage temp. −20°C
solubility H2O: ≥2 mg/mL
form powder
pka 3.06±0.10(Predicted)
color green
FDA UNII 6E47VKF8B8

SAFETY

Risk and Safety Statements

Hazard Codes  Xi
Risk Statements  36/37/38
Safety Statements  26-36
WGK Germany  3

SNAP price More Price(5)

Manufacturer Product number Product description CAS number Packaging Price Updated Buy
TRC N522050 S-Nitroso-N-acetyl-D-β,β-dimethylcysteine 79032-48-7 10mg $130 2021-12-16 Buy
American Custom Chemicals Corporation AAA0006365 N-ACETYL-3-(NITROSOTHIO)-D-VALINE 95.00% 79032-48-7 10MG $142.8 2021-12-16 Buy
ApexBio Technology B6368 SNAP 79032-48-7 50mg $471 2021-12-16 Buy
ApexBio Technology B6368 SNAP 79032-48-7 10mg $108 2021-12-16 Buy
Product number Packaging Price Buy
N522050 10mg $130 Buy
AAA0006365 10MG $142.8 Buy
B6368 50mg $471 Buy
B6368 10mg $108 Buy

SNAP Chemical Properties,Uses,Production

Chemical Properties

Green Crystalline Solid

Uses

The D-isomer of SNAP. Serves as an NO donor.

Definition

ChEBI: A nitroso compound that is N-acetyl-D-penicillamine in which the sulfanyl hydrogen is replaced by a nitroso group.

General Description

Nitric oxide donor that begins to evolve nitric oxide immediately upon solubilization in aqueous buffers (t1/2 = 10 h). Mimics the actions of nitric oxide, including the relaxation of isolated bovine coronary artery rings (EC50 = 130 nM). Markedly activates soluble guanylate cyclase. Also reported to cause the reversible inactivation of protein kinase C activity. Induces apoptosis in mouse thymocytes. Note: 1 set = 4 x 5 mg.

Biological Activity

A stable analog of endogenous S-nitroso compounds. A source of NO in vivo which unlike organic O-nitrates does not induce tolerance. Decomposes slowly in solution with a t ?of 37h.

Biochem/physiol Actions

EC50 = 130 nM in relaxation of isolated bovine coronary artery rings

storage

Store at -20°C

SNAP Preparation Products And Raw materials

Raw materials

Preparation Products

Global( 34)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 32161 58
J & K SCIENTIFIC LTD. 010-82848833 400-666-7788 jkinfo@jkchemical.com China 96815 76
3B Pharmachem (Wuhan) International Co.,Ltd. 821-50328103-801 18930552037 3bsc@sina.com China 15839 69
Chemsky(shanghai)International Co.,Ltd. 021-50135380 shchemsky@sina.com China 32321 50
EMMX Biotechnology LLC 888-539-0666 info@emmx.com United States 8447 60
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9806 58
Shanghai Rechem science Co., Ltd. 21-31433387 15618786686 sales@rechemscience.com China 2988 58
Henan Weituxi Chemical Technology Co., Ltd. 0371-63284658 18135795563 2885349392@qq.com China 10003 58
Jiangsu Hongmin Pharmaceutical Co., Ltd. 18221292452 fannieliu@glschina.com China 6798 58
MedBioPharmaceutical Technology Inc 021-69568360 18916172912 order@med-bio.cn China 8140 58
S-Nitroso-acetyl penicillamine 2-acetamido-3-methyl-3-(nitrosothio)butyric acid 2-acetamido-3-methyl-3-nitrososulfanylbutanoic acid 2-acetamido-3-methyl-3-nitrososulfanyl-butanoic acid N-Acetyl-S-nitroso-D-penicillaMine N-ACETYL-3-(NITROSOTHIO)-D-VALINE SNAP SNAP(D) S-NITRO-N-ACETYL-D,L-PENACILLAMINE S-NITROSO-N-ACETYL-D-BETA,BETA-DIMETHYLCYSTEINE S-NITROSO-N-ACETYLPENICILLAMINE S-NITROSO-N-ACETYLPENICILLAMINE (SNAP) P OTENT VASODILATOR S-Nitroso-N-acetyl-D-b,b-dimethylcysteine S-nitroso-N-acetyl-D-penicillamine S-Nitroso-N-acetyl-D-β,β-dimethylcysteine D-Valine, N-acetyl-3-(nitrosothio)- 79032-48-7 Nitric Oxide Metabolism Enzymes, Inhibitors, and Substrates BioChemical Biochemicals and Reagents Cell Signaling Enzymes Application Index NO Donors Nitric Oxide Reagents Nitric Oxide