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Ertapenem

HCID 150610
노트반응

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기본 정보이름 및 식별자물성안전 및 규제화학 및 산업관련 반응화합물 노트
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기본 정보

CAS
153773-82-1
표준 SMILES
C[C@@H](O)[C@H]1C(=O)N2C(C(=O)O)=C(S[C@@H]3CN[C@H](C(=O)Nc4cccc(C(=O)O)c4)C3)[C@H](C)[C@H]12
InChIKey
JUZNIMUFDBIJCM-ANEDZVCMSA-N
분자식
C22H25N3O7S
평균 분자량
475.523 g/mol
단동위원소 질량
475.14132114

이름 및 식별자

우선 이름
Ertapenem
IUPAC
(4R,5S,6S)-3-({(3S,5S)-5-[(3-Carboxyphenyl)carbamoyl]pyrrolidin-3-yl}sulfanyl)-6-(1-hydroxyethyl)-4-methyl-7-oxo-1-azabicyclo[3.2.0]hept-2-ene-2-carboxylic acid
영어명
Ertapenem
분자식
C22H25N3O7S
분자량
475.51

이름 및 동의어

Ertapenem hydrochlorideMK-0826EOS-61119ERTAPENEMErtapenem D4Ertapenem PowderErtapenem MonomerErtapenem USP/EP/BPERTAPENEM(FORR&DONLY)ErtapenemDiscontinued See E635000

데이터베이스 식별자

CAS
153773-82-1、153832-46-3
PubChem CID
150610
DTXSID
DTXSID50165456
ChEMBL
CHEMBL1359
ChEBI
CHEBI:404903
UNII
G32F6EID2H
EC Number
836-232-1
Nikkaji
J2.766.498I

물성

물리화학적 성질

끓는 점
813.9 · 813.9±65.0 °C(Predicted)
밀도
1.55 · 1.55±0.1 g/cm3(Predicted)
저장 조건
2 · 2-8°C
용해도
메탄올,DMSO에 용해됨
산도 계수 (pKa)
4.03 · 4.03±0.10(Predicted)
물리적 상태
포말 모양
색상
갈색
InChIKey
JUZNIMUFDBIJCM-ANEDZVCMSA-N
SMILES
N12[C@@]([H])([C@@H]([C@H](O)C)C1=O)[C@@H](C)C(S[C@H]1C[C@@H](C(NC3=CC=CC(C(O)=O)=C3)=O)NC1)=C2C(O)=O

안전 및 규제

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

안전 데이터

유해 물질 데이터
153832-46-3(Hazardous Substances Data)

화학 및 산업

응용 분야 · 3건

개요Ertapenem is another synthetic carbapenem with a rather complex side chain at C-3. It is used once daily parenterally, with special application against anaerobes. As with meropenem, the 4-β-methyl group confers stability toward dehydropeptidase-1 It is not active against pseudomonads or acinetobacteria and, therefore, should not be substituted for imipenem or meropenem. It is relatively strongly bound to serum proteins, so it has a prolonged half-life, making it more convenient to use than the other carbapenems when its spectrum warrants this. Its reported indications include complicated intra-abdominal and complicated skin/skin structure infections caused by sensitive organisms (for intra-abdominal: Escheri chia coli, Clostri di um clostri doforme, Bacteroi des fragilis, and Peptostreptococcus sp; for skin/skin structures: Staphylococcus aureus (methicillin-susceptible strains), Streptococcus pyogenes, E.coli, or Peptostreptococcus sp.). It can be administered once daily.

용도Ertapenem is a long-acting parenteral cabapenem. Ertapenem has bactericidal activity against a variety of gram-negative pathogens, some gram positive strains, and Haemopilus influenzae. Ertapenem has shown to inactivate L,D-transpeptidase, an enzyme responsible for in vitro cross-linking of Mycobacterium tuberculosis peptidoglycan.

일반 설명Ertapenem (Invanz, for injection) is a synthetic 1-β-methylcarbapenem that is structurally related to β-lactam antibiotics,particularly the thienamycin group. Its mechanism ofaction is the same as that of other β-lactam antibiotics. Thestructure resists β-lactamases and dehydropeptidases.Ertapenem is indicated for the treatment of moderate tosevere infections caused by susceptible strains causing complicatedintra-abdominal infections such as Escherichia,Clostridium, Peptostreptococcus, and Bacteroides. Theantibiotic is also indicated for complicated skin and skinstructure infections including diabetic foot infections (withoutosteomyelitis). Treatable strains include Staphylococcus(MSSA), Streptococcus, Escherichia, Klebsiella, Proteus,and Bacteroides. Ertapenem is also indicated for community-acquired pneumonia caused by S. pneumoniae,Haemophilus infljuenzae, and M. catarrhalis. Complicatedurinary tract infections and acute pelvic infections round outthe indications for ertapenem.

공급사100 곳

北京华美互利生物化工

관련 반응

5건
반응 기록 만들기
HRID 2067708 반응식
HRID 2067708생성물로uspto-grants-2012_10
HRID 2067709 반응식
HRID 2067709반응물로uspto-grants-2012_10
HRID 2067710 반응식
HRID 2067710반응물로uspto-grants-2012_10
HRID 2067711 반응식
HRID 2067711반응물로uspto-grants-2012_10
HRID 2068129 반응식
HRID 2068129반응물로uspto-grants-2012_10

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추가 설명 · 1건

정의ChEBI: Meropenem in which the one of the two methyl groups attached to the amide nitrogen is replaced by hydrogen while the other is replaced by a 3-carboxyphenyl group. The sodium salt is used for the treatment of moderate to severe susceptible infections includ ng intra-abdominal and acute gynaecological infections, pneumonia, and infections of the skin and of the urinary tract.