✉ info@591daili.com☎ +86-18553102138
📞 WhatsApp中文
591daili 济南圣和化工
Home › Product Catalog › Nafamostat Mesylate

Nafamostat Mesylate

CAS 82956-11-4C21H25N5O8S2MW 539.6

Nafamostat Mesylate (CAS 82956-11-4) — formula C21H25N5O8S2, molecular weight 539.6; category organic chemicals.

Specifications

CAS Number82956-11-4
Molecular FormulaC21H25N5O8S2
Molecular Weight539.6
CategoryOrganic Chemicals

Purchase Profile

What this product is

Nafamostat Mesylate is a carbon-based organic compound with CAS registry number 82956-11-4 and molecular formula C21H25N5O8S2 (molecular weight 539.6), belonging to the organic chemicals segment of chemical raw materials.

Identification

CAS number: 82956-11-4

Its molecular formula C21H25N5O8S2 comprises 21 C, 25 H, 5 N, 8 O, 2 S atoms.

Also known as: Nafamostat Mesylate

Category: organic chemicals

Frequently Asked Questions

What is the CAS number of Nafamostat Mesylate?

The CAS registry number of Nafamostat Mesylate is 82956-11-4.

What is the molecular formula and molecular weight of Nafamostat Mesylate?

Molecular formula C21H25N5O8S2, molecular weight 539.6.

What other names is Nafamostat Mesylate known by?

It is also registered under: Nafamostat Mesylate.

Which category does Nafamostat Mesylate belong to?

Category: Organic Chemicals.

PubChem Public Data

Public-database records for Nafamostat Mesylate (CAS 82956-11-4), reproduced here for independent cross-checking.

Safety classification and hazard statements

Reported hazard statementsH361 (95.3%)

H361 (95.3%): Suspected of damaging fertility or the unborn child [Warning Reproductive toxicity]

P203, P280, P318, P405, and P501 (click each P-code to see the statement)

How this substance is indexed

CAS Registry Number82956-11-4
PubChem CID5311180
分子式C21H25N5O8S2
IUPAC 名称(6-carbamimidoylnaphthalen-2-yl) 4-(diaminomethylideneamino)benzoate;methanesulfonic acid
UNII(FDA)1D2T74921W

Documented uses

  • Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects.
  • Agents that prevent BLOOD CLOTTING.
  • Compounds which inhibit or antagonize biosynthesis or actions of proteases (ENDOPEPTIDASES).
  • Serine proteinase inhibitors which inhibit trypsin. They may be endogenous or exogenous compounds.
  • Exogenous or endogenous compounds which inhibit SERINE ENDOPEPTIDASES.
  • Compounds that negatively regulate the cascade process of COMPLEMENT ACTIVATION. Uncontrolled complement activation and resulting cell lysis is potentially dangerous for the host.

Names this substance appears under

Nafamostat mesylate; 82956-11-4; nafamostat mesilate; FUT-175; Nafamstat Mesilate; Ronastat; Nafamostat dimethanesulfonate; 1D2T74921W; Benzoic acid, 4-[(aminoiminomethyl)amino]-, 6-(aminoiminomethyl)-2-naphthalenyl ester, dimethanesulfonate; DTXSID7046128; FUT 175; 6-Amidino-2-naphthyl 4-guanidinobenzoate dimethanesulfonate; CKD-314; Benzoic acid, 4-((aminoiminomethyl)amino)-, 6-(aminoiminomethyl)-2-naphthalenyl ester, dimethanesulfonate; RefChem:164397; FUT175

Computed molecular descriptors

分子量539.6
氢键供体数6
氢键受体数10
可旋转键数5
精确质量539.11445512
单同位素质量539.11445512
拓扑极性表面积266
重原子数36
形式电荷0
复杂度645

Database abstract

Nafamostat Mesylate · CAS 82956-11-4 · C21H25N5O8S2. UNII 1D2T74921W.

Source: PubChem / Wikidata; the batch COA governs where values differ.

You may also need

Get a quote for Nafamostat Mesylate

Supplier: Jinan Shenghe Chemical Co., Ltd. · Reply within one business day.

Email Inquiry WhatsApp
鲁ICP备19031700号-1