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Home > Encyclopedia > 2-acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid

2-acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid

2-acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid structure

2-acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid 

structure
  • CAS No:

    67776-06-1

  • Formula:

    C7H12N2O4S

  • Chemical Name:

    2-acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid

  • Synonyms:

    N-(ACETYLOXY)-3-NITROSOTHIOVALINE;SNAP;(+/-)-S-NITROSO-N-ACETYLPENICILLAMINE;S-NITROSO-N-ACETYL-D,L-PENICILLAMINE;S-Nitroso-N-acetyl-DL-penicillamine,N-Acetyl-3-(nitrosothio)-DL-valine, S-Nitroso-N-acetylpenicillamine, SNAP;(R)-2-acetaMido-3-Methyl-3-(nitrosothio)butanoic acid;SNAP [S-Nitroso-N-acetylpenicillaMine];Anti-SNAP25, C-Terminal antibody produced in rabbit

  • Categories:

    Biochemical Engineering  >  Amino Acids and Derivatives

Description

S-Nitroso-N-acetyl-DL-penicillamine (SNAP) is a nitric oxide donor and acts as a stable inhibitor of platelet aggregation[1][2][3][4].


A sulfur-containing alkyl thionitrite that is one of the NITRIC OXIDE DONORS.


SNAP is an S-nitrosothiol which serves as a NO donor and a potent vasodilator. Its stability in solution varies from seconds to hours depending on temperature, buffer composition and metal content. At pH 6-8 and 37°C, the half-life of SNAP is approximately six hours in the presence of transition metal ion chelators.


2-acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid is green crystalline solid

2-acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid Basic Attributes

220.25

220.25

312630

green

Characteristics

121

1.13

green powder

1.4261 (rough estimate)

150.5°C

1.5400 (estimate)

H2O: ≥2mg/mLDMSO: ≥20mg/mL, clear (faint green to very dark green)

−20°C

3.06±0.10(Predicted)

-20°C

Safety Information

NONH for all modes of transport

3

Xi

26-36

YV9383000

Xi

P261-P305 + P351 + P338

36/37/38

|Warning|H315 (100%): Causes skin irritation [Warning Skin corrosion/irritation]|P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, and P501|Aggregated GHS information provided by 38 companies from 1 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

Drug Information

A diverse group of agents, with unique chemical structures and biochemical requirements, which generate NITRIC OXIDE. These compounds have been used in the treatment of cardiovascular diseases and the management of acute myocardial infarction, acute and chronic congestive heart failure, and surgical control of blood pressure. (Adv Pharmacol 1995;34:361-81) (See all compounds classified as Nitric Oxide Donors.)|Compounds or agents that combine with an enzyme in such a manner as to prevent the normal substrate-enzyme combination and the catalytic reaction. (See all compounds classified as Enzyme Inhibitors.)|Drugs used to cause dilation of the blood vessels. (See all compounds classified as Vasodilator Agents.)

N-Acetyl-S-Nitrosopenicillamine

2-acetamido-3-methyl-3-(nitrososulfanyl)butanoic acid Use and Manufacturing

Produced concentration-related relaxations of mouse anococcygeus, in a range similar to that already found for NO and other nitrovasodilators. A potent relaxant of non-vascular smooth muscle. Serves as an NO donor.

Computed Properties

Molecular Weight:220.25
XLogP3:-0.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:4
Exact Mass:220.05177804
Monoisotopic Mass:220.05177804
Topological Polar Surface Area:121
Heavy Atom Count:14
Complexity:254
Undefined Atom Stereocenter Count:1
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes

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