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ヘタシリン

Hetacillin

HCID 443387
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
3511-16-8
標準SMILES
CC1(C)S[C@@H]2[C@H](N3C(=O)[C@@H](c4ccccc4)NC3(C)C)C(=O)N2[C@H]1C(=O)O
InChIKey
DXVUYOAEDJXBPY-NFFDBFGFSA-N
分子式
C19H23N3O4S
平均分子量
389.5 g/mol
単同位体質量
389.1409274

概要

Hetacillin is a penicillin. It has a role as an antibacterial drug. It is a conjugate acid of a hetacillin(1-).

名称と識別子

優先名称
Hetacillin
IUPAC
(2S,5R,6R)-6-[(4R)-2,2-dimethyl-5-oxo-4-phenylimidazolidin-1-yl]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
現地名
ヘタシリン
英語名
7-(2,2-Dimethyl-5-oxo-4-phenyl-imidazolidin-1-yl)-3,3-dimethyl-6-oxo-2-thia-5-azabicyclo[3.2.0]heptane-4-carboxylic acid
分子式
C19H23N3O4S
分子量
389.47

名称と別名

hetacillin3511-16-8HetacilinaHetacillineHetacillinumVersapenPhenazacillinHetacillin acidBL-P 804BRL-804(2S,5R,6R)-6-[(4R)-2,2-dimethyl-5-oxo-4-phenylimidazolidin-1-yl]-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acidTN4JSC48CV
名称をさらに表示
ヘタシリンペンプレヌームエタシリン(2S,5R,6R)-6-[(4R)-2,2-ジメチル-5-オキソ-4-フェニルイミダゾリジン-1-イル]-3,3-ジメチル-7-オキソ-4-チア-1-アザビシクロ[3.2.0]ヘプタン-2-カルボン酸ベルサペン(2S,5β)-6α-[(4R)-2,2-ジメチル-5-オキソ-4-フェニル-1-イミダゾリジニル]-3,3-ジメチル-7-オキソ-4-チア-1-アザビシクロ[3.2.0]ヘプタン-2β-カルボン酸ビモシリンフェナザシリンPenplenumHetacillin USP/EP/BP6-(2,2-dimethyl-5-oxo-4-phenylimidazolidin-1-yl)penicillanic acid6-[2,2-Dimethyl-5-oxo-4-phenyl-1-imidazolidinyl] penicillanic acid
BL-P-804BLP-804CHEBI:5683DTXSID4023121N,N'-Isopropylidene-A-amino-benzyl penicillin6-(2,2-Dimethyl-5-oxo-4-phenyl-1-imidazolidinyl)-3,3-dimethyl-7-oxo-4-thia-1-azabicyclo(3.2.0)heptane-2-carboxylic acid6beta-[(4R)-2,2-dimethyl-5-oxo-4-phenylimidazolidin-1-yl]penicillanic acidHetacin

データベース識別子

CAS
3511-16-8
PubChem CID
443387
DTXSID
DTXSID4023121
ChEMBL
CHEMBL1201116
ChEBI
CHEBI:5683
UNII
TN4JSC48CV
EC Number
222-512-5
Nikkaji
J7.741K

物性

構造計算による物性

XLogP
-0.6
極性表面積
115 Ų
水素結合供与体数
2
水素結合受容体数
6
回転可能結合数
3
重原子数
27
形式電荷
0
複雑度
688

実験および物理化学的性質

DrugsPharmaceuticals -> Listed in ZINC15
LogP1.3
Solubility5.12e-01 g/L
Human Drugs · 2 件

FDA approved drugs -> Active ingredient

FDA approved drugs -> Active ingredient

Melting Point190 °C
Physical DescriptionSolid
Collision Cross Section189.39 Ų [M+H]+ [CCS Type: TW; Method: calibrated with polyalanine and drug standards]

物理化学的性質

融点
189.2 · 189.2-191.0°
比旋光度
25 · D25 +366° (pyridine)
沸点
648.4 · 648.4±55.0 °C(Predicted)
比重(密度)
1.43 · 1.43±0.1 g/cm3(Predicted)
貯蔵温度
-20 °C · Hygroscopic, -20°C Freezer, Under inert atmosphere
溶解性
DMSO(微量)、メタノール(微量)、ピリジン(微量)
外見
個体
酸解離定数(Pka)
2.45 · 2.45±0.50(Predicted)
色
ホワイトからオフホワイト
安定性
吸湿性、溶液中で不安定

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

Danger

H317 (100%): May cause an allergic skin reaction [Warning Sensitization, Skin]

P233, P260, P261, P271, P272, P280, P284, P302+P352, P304+P340, P321, P333+P317, P342+P316, P362+P364, P403, and P501 (click each P-code to see the statement)

Aggregated GHS information provided per 40 reports by companies from 1 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 CategoriesSkin Sens. 1 (100%)

安全データ

危険有害性情報
コード 危険有害性情報 危険有害性クラス 区分 注意喚起語 シンボル P コード H317

化学と産業

薬理情報

ATC Code · 2 件

J - Antiinfectives for systemic use

QJ - Antiinfectives for systemic use

Pharmacodynamics · 1 件

Hetacillin is a penicillin beta-lactam antibiotic used in the treatment of bacterial infections caused by susceptible, usually gram-positive, organisms. The name "penicillin" can either refer to several variants of penicillin available, or to the group of antibiotics derived from the penicillins. Hetacillin has in vitro activity against gram-positive and gram-negative aerobic and anaerobic bacteria. The bactericidal activity of Hetacillin results from the inhibition of cell wall synthesis and is mediated through Hetacillin binding to penicillin binding proteins (PBPs).

Mechanism of Action · 1 件

Hetacillin is a semisynthetic penicillin prodrug which itself has no antibacterial activity, but is converted in the body to ampicillin and has actions and uses similar to those of ampicillin. Hetacillin is prepared by reacting ampicillin with acetone. Ampicillin rapidly decomposes because of the intramolecular attack of the side chain amino group on the lactam ring. _In vitro_ studies have shown that hetacillin is resistant to beta lactamase activity. However, this effect is transient, as the hydrolysis product, ampicillin, is readily inactivated by beta lactamase. Hetacillin locks up the offending amino group and prevents the decomposition of Hetacillin. Once hydrolyzed to ampicillin (and acetone), ampicillin binds to the penicillin binding proteins found in susceptible bacteria. This inhibits the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins.

Metabolism/MetabolitesHydrolyzed to active ampicillin via esterases
Cellular LocationsMembrane
応用分野 · 2 件

説明Hetacillin was synthesized by Bristol-Myers Laboratories in 1964. It shows activity as strong as that of ampicillin against a variety of gram-positive and gram-negative bacteria. Hetacillin shows almost the same pharmacokinetic properties as ampicillin when administered orally and a later serum peak when given by intramuscular administration. When administered either orally or intramuscularly, it is hydrolyzed in vivo into ampicillin. Therefore, the clinical applications of hetacillin are the same as those of ampicillin.

使用Antibacterial.

上流・下流製品情報

上流原料

アセトン

サプライヤー23 社

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関連反応

1 件
反応記録を作成
HRID 1855929 の反応式
HRID 1855929反応物としてuspto-grants-1980_08

化合物ノート

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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