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酢酸マフェニド

Mafenide Acetate

HCID 25590
ノート反応
基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
部分構造検索類似構造を探す

基本情報

CAS
13009-99-9
標準SMILES
CC(=O)O.NCc1ccc(S(N)(=O)=O)cc1
InChIKey
UILOTUUZKGTYFQ-UHFFFAOYSA-N
分子式
C9H14N2O4S
平均分子量
246.29 g/mol
単同位体質量
246.06742793

概要

Mafenide acetate is a carboxylic acid.

名称と識別子

優先名称
Mafenide Acetate
IUPAC
acetic acid;4-(aminomethyl)benzenesulfonamide
現地名
酢酸マフェニド
英語名
Mafenide acetate
分子式
C9H14N2O4S
分子量
246.28

名称と別名

MAFENIDE ACETATE13009-99-9SulfamilonBenzenesulfonamide, 4-(aminomethyl)-, monoacetateRQ6LP6Z0WYalpha-Amino-p-toluenesulfonamide monoacetate4-(Aminomethyl)benzenesulfonamide monoacetateDTXSID00156334RefChem:55527DTXCID0078825NSC346324-(AMINOMETHYL)BENZENESULFONAMIDE ACETATE
名称をさらに表示
4-(アミノメチル)ベンゼンスルホンアミド·酢酸酢酸マフェニド4-(アミノメチル)ベンゼンスルホンアミド酢酸塩酢酸4-(アミノメチル)ベンゼンスルホンアミド酢酸マフェニド (JAN)4-(アミノメチル)ベンゼンスルホンアミド・酢酸MAFENIDEMefamideMARFANILmaphenideacetateSulfamylon AcetateMafenidine AcetateMAFENAMIDE ACETATESulfamimeron acetate
Mafenide (Acetate)MFCD00072089Benzenesulfonamide, 4-(aminomethyl)-, acetate (1:1)acetic acid;4-(aminomethyl)benzenesulfonamideMafatateMafenide acetate (JAN/USP)MAFENIDE ACETATE [MI]HMS2231M06

データベース識別子

CAS

物性

構造計算による物性

極性表面積
132 Ų
水素結合供与体数
3
水素結合受容体数
6
回転可能結合数
2
重原子数
16
形式電荷
0
複雑度
255

実験および物理化学的性質

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

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

物理化学的性質

融点
151 · 151-152°C
貯蔵温度
2 · Inert atmosphere,2-8°C
溶解性
1 mg/mL · DMSO:可溶1mg/mL
外見
個体
色
白い
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
CAS データベース
13009 · 13009-99-9(CAS DataBase Reference)

化学的性質

化学的特性Mafenide acetate, USP is a white, crystalline powder which is freely soluble in water.

安全と法規制

安全情報は参考情報です。供給元の安全データシート(SDS)、適用法令、専門家による評価に代わるものではありません。

GHS分類

GHS Classification · 4 件

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.

危険有害性情報

Hazard Classes and CategoriesAcute Tox. 4 (100%)

安全データ

wgk
3
毒性
LD50 in rats, mice (mg/kg): 2040, 1580 i.v. (Skulan, Hoppe)
hs_code
2935904000
hazard_class
IRRITANT
ストレージクラス
11 - Combustible Solids

化学と産業

薬理情報

FDA Pharmacological Classification · 2 件

MAFENIDE ACETATE

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

MeSH Pharmacological Classification · 3 件

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.

応用分野 · 2 件

説明Mafenide 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.

一般的な説明4-(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.

上流・下流製品情報

関連反応

1 件
反応記録を作成
HRID 68234 の反応式
HRID 68234生成物としてuspto-grants-2014_09

化合物ノート

読み込み中…

このページの内容基本情報概要名称と識別子物性安全と法規制化学と産業関連反応化合物ノート
13009-99-9
PubChem CID
25590
DTXSID
DTXSID00156334
ChEMBL
CHEMBL1201161
ChEBI
CHEBI:31792
UNII
RQ6LP6Z0WY
EC Number
235-855-0

上流原料

アンモニアクロロスルホン酸N-ベンジルアセトアミド

サプライヤー100 社

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