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마페니드아세테이트

Mafenide Acetate

HCID 25590
노트반응
기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
부분 구조 검색유사 구조 찾기

기본 정보

CAS
13009-99-9
표준 SMILES
CC(=O)O.NCc1ccc(S(N)(=O)=O)cc1
InChIKey
UILOTUUZKGTYFQ-UHFFFAOYSA-N
분자식
C9H14N2O4S
평균 분자량
246.29 g/mol
단동위원소 질량
246.06742793

개요

Mafenide acetate is a carboxylic acid.

이름 및 식별자

우선 이름
Mafenide Acetate
IUPAC
acetic acid;4-(aminomethyl)benzenesulfonamide
현지명
마페니드아세테이트
영어명
Mafenide acetate
분자식
C9H14N2O4S
분자량
246.28

이름 및 동의어

MAFENIDE ACETATE13009-99-9SulfamilonBenzenesulfonamide, 4-(aminomethyl)-, monoacetateRQ6LP6Z0WYalpha-Amino-p-toluenesulfonamide monoacetate4-(Aminomethyl)benzenesulfonamide monoacetateDTXSID00156334RefChem:55527DTXCID0078825NSC346324-(AMINOMETHYL)BENZENESULFONAMIDE ACETATE
이름 더 보기
마페니드아세테이트MAFENIDEMefamideMARFANILmaphenideacetateSulfamylon AcetateMafenidine AcetateMAFENAMIDE ACETATESulfamimeron acetate
Mafenide (Acetate)MFCD00072089Benzenesulfonamide, 4-(aminomethyl)-, acetate (1:1)acetic acid;4-(aminomethyl)benzenesulfonamideMafatateMafenide acetate (JAN/USP)MAFENIDE ACETATE [MI]HMS2231M06

데이터베이스 식별자

CAS
13009-99-9
PubChem CID
25590
DTXSID
DTXSID00156334
ChEMBL
CHEMBL1201161

물성

구조 계산 물성

극성 표면적
132 Ų
수소 결합 공여자 수
3
수소 결합 수용자 수
6
회전 가능 결합 수
2
무거운 원자 수
16
형식 전하
0
복잡도
255

실험 및 물리화학적 성질

Solubility>36.9 [ug/mL] (The mean of the results at pH 7.4)
Human Drugs · 2건

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

물리화학적 성질

녹는점
151 · 151-152°C
저장 조건
2 · Inert atmosphere,2-8°C
용해도
1 mg/mL · DMSO: 용해성1mg/mL
물리적 상태
고체
색상
하얀색
InChI
InChI=1S/C7H10N2O2S.C2H4O2/c8-5-6-1-3-7(4-2-6)12(9,10)11;1-2(3)4/h1-4H,5,8H2,(H2,9,10,11);1H3,(H,3,4)
InChIKey
UILOTUUZKGTYFQ-UHFFFAOYSA-N
SMILES
C1(=CC=C(CN)C=C1)S(=O)(=O)N.C(=O)(O)C

화학적 성질

Mafenide acetate, USP is a white, crystalline powder which is freely soluble in water.

안전 및 규제

안전 정보는 참고용이며, 공급업체의 물질안전보건자료(SDS), 관련 법규 및 전문가 평가를 대체하지 않습니다.

GHS 분류

GHS Classification · 4건

Warning

H302 (100%): Harmful if swallowed [Warning Acute toxicity, oral]

P261, P264, P264+P265, P270, P271, P280, P301+P317, P302+P352, P304+P340, P305+P351+P338, P319, P321, P330, P332+P317, P337+P317, P362+P364, P403+P233, P405, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 2 reports by companies from 2 notifications to the ECHA C&L Inventory. Each notification may be associated with multiple companies.

유해성 정보

Hazard Classes and CategoriesAcute Tox. 4 (100%)

안전 데이터

wgk
3
독성
LD50 in rats, mice (mg/kg): 2040, 1580 i.v. (Skulan, Hoppe)
HS 번호
2935904000
위험 등급
IRRITANT
스토리지 클래스
11 - Combustible Solids

화학 및 산업

약리 정보

FDA Pharmacological Classification · 2건

MAFENIDE ACETATE

Methylated Sulfonamides [EXT]; Methylated Sulfonamide Antibacterial [EPC]

MeSH Pharmacological Classification · 3건

Substances used on humans and other animals that destroy harmful microorganisms or inhibit their activity. They are distinguished from DISINFECTANTS, which are used on inanimate objects.

A class of compounds that reduces the secretion of H+ ions by the proximal kidney tubule through inhibition of CARBONIC ANHYDRASES.

Substances that inhibit the growth or reproduction of BACTERIA.

응용 분야 · 2건

개요Mafenide Acetate, also known sulfamylon acetate, is a topical sulphonamide antimicrobial agent with activity against a wide range of microorganisms commonly associated with burn wound infections, including Pseudomonas aeruginosa and Staphylococcus aureus. It is primarily used for the prevention and treatment of burn wound infections. As a carbonic anhydrase inhibitor, sulfamylon acetate may cause metabolic acidosis and peripheral vasodilation. Therefore, its concomitant use with hyperbaric oxygen therapy should be carefully assessed. In burn patients requiring hyperbaric oxygen therapy, silver sulfadiazine may be considered as an alternative topical antimicrobial agent.

일반 설명4-(Aminomethyl)benzenesulfonamide acetate (Sulfamylon)is a homologue of the sulfanilamide molecule. It is not atrue sulfanilamide-type compound, as it is not inhibited byPABA. Its antibacterial action involves a mechanism thatdiffers from that of true sulfanilamide-type compounds. This compound is particularly effective against Clostridiumwelchii in topical application and was used duringWorld War II by the German army for prophylaxis ofwounds. It is not effective orally. It is currently used aloneor with antibiotics in the treatment of slow-healing, infectedwounds.Some patients treated for burns with large quantities ofthis drug have developed metabolic acidosis. To overcomethis adverse effect, a series of new organic salts was prepared. The acetate in an ointment base proved to be themost efficacious.

상·하류 제품 정보

관련 반응

1건
반응 기록 만들기
HRID 68234 반응식
HRID 68234생성물로uspto-grants-2014_09

화합물 노트

불러오는 중…

이 페이지에서기본 정보개요이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
ChEBI
CHEBI:31792
UNII
RQ6LP6Z0WY
EC Number
235-855-0

상류 원료

암모니아(가스)클로로술폰산N-벤질아세트아미드

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