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Sulotroban

HCID 51550
NotesReactions
Basic informationOverviewNames & identifiersPropertiesChemistry & industryRelated reactionsCompound notes
Substructure searchFind similar structures

Basic information

CAS
72131-33-0
Standard SMILES
O=C(O)COc1ccc(CCNS(=O)(=O)c2ccccc2)cc1
InChIKey
XTNWJMVJVSGKLR-UHFFFAOYSA-N
Molecular formula
C16H17NO5S
Average molar mass
335.4 g/mol
Monoisotopic mass
335.08274382

Overview

Sulotroban is a small molecule drug. Sulotroban has a monoisotopic molecular weight of 335.08 Da.

Names & identifiers

Preferred name
Sulotroban
IUPAC
2-[4-[2-(benzenesulfonamido)ethyl]phenoxy]acetic acid
English name
Sulotroban
Molecular formula
C16H17NO5S
Molecular weight
335.37

Names & synonyms

SULOTROBAN72131-33-0BM-13177SKF-95587SulotrobanumSK&F 95587BM 13.177SK&F-95587SKF 95587Acetic acid, (4-(2-((phenylsulfonyl)amino)ethyl)phenoxy)-(p-(2-Benzenesulfonamidoethyl)phenoxy)acetic acidSKF95587
Show more names
Sulotraban4-[2-[(Phenylsulfonyl)amino]ethyl]phenoxyacetic acidAcetic acid, 2-[4-[2-[(phenylsulfonyl)aMino]ethyl]phenoxy]-
4-(2-(benzenesulfonamido)ethyl)phenoxyacetic acid74574CO5A6BM13177BM-13.177DTXSID80222440RefChem:932400DTXCID80144931BM 13177

Database identifiers

CAS
72131-33-0
PubChem CID
51550
DTXSID
DTXSID80222440
ChEMBL
CHEMBL8273
UNII
74574CO5A6
Nikkaji
J21.727A

Properties

Computed structural properties

XLogP
2.4
Topological polar surface area
101 Ų
Hydrogen bond donors
2
Hydrogen bond acceptors
6
Rotatable bonds
8
Heavy atoms
23
Formal charge
0
Complexity
459

Physicochemical properties

Boiling point
551.7 · 551.7±60.0 °C(Predicted)
Density
1.328 · 1.328±0.06 g/cm3(Predicted)
form
Solid
pka
3.19 · 3.19±0.10(Predicted)
FDA UNII
74574 CO5A6 · 74574CO5A6

Chemistry & industry

Pharmacology

MeSH Pharmacological Classification · 3 items

Agents used for the treatment or prevention of cardiac arrhythmias. They may affect the polarization-repolarization phase of the action potential, its excitability or refractoriness, or impulse conduction or membrane responsiveness within cardiac fibers. Anti-arrhythmia agents are often classed into four main groups according to their mechanism of action: sodium channel blockade, beta-adrenergic blockade, repolarization prolongation, or calcium channel blockade.

Fibrinolysin or agents that convert plasminogen to FIBRINOLYSIN.

Drugs or agents which antagonize or impair any mechanism leading to blood platelet aggregation, whether during the phases of activation and shape change or following the dense-granule release reaction and stimulation of the prostaglandin-thromboxane system.

Applications

UsesGlomerulonephritis treatment.

Suppliers6 total

Hangzhou Sage Chemical Co., Ltd.+86057186818502 13588463833 · [email protected]
上海寰川实业有限公司021-61478794 · [email protected]
上海陶术生物科技股份有限公司+1-781-999-5354; +1-00000000000 · [email protected]
上海一飞生物科技有限公司021-65675885 18964387627 · [email protected]
TargetMol中国(陶术生物)15002134094 · [email protected]
上海阿摩尔生物科技有限公司13370042665 18916960931 · [email protected]

Related reactions

2 records
New reaction record
HRID 945782 reaction equation
HRID 945782As reactantValidation data from https://doi.org/10.1039/C8SC04228D
HRID 1709269 reaction equation
HRID 1709269As reactantuspto-grants-1990_08

Compound notes

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