기본 정보
- 표준 SMILES
CO[C@H]1[C@@H](O)[C@H](N)[C@@H](O[C@H]2O[C@H]([C@H](C)N)CC[C@H]2N)[C@H](O)[C@@H]1N(C)C(=O)CN- InChIKey
BIDUPMYXGFNAEJ-APGVDKLISA-N- 분자식
- C17H35N5O6
- 평균 분자량
- 405.5 g/mol
- 단동위원소 질량
- 405.25873384
개요
Astromicin is an amino cyclitol glycoside that is L-chiro-inositol in which the hydroxy groups at positions 1, 4, and 6 are replaced by aminoacetyl)methylamino, amino, and methoxy groups, respectively, and in which the hydroxy group at position 3 is converted to the corresponding 2,6-diamino-2,3,4,6,7-pentadeoxy-beta-L-lyxo-heptopyranoside. The major component of fortimicin, obtained from Micromonospora olivasterospora. It is administered (as the sulfate salt) by intramuscular injection or intravenous infusion for the treatment of severe systemic infections due to sensitive Gram-negative organisms. It has a role as a metabolite and an antibacterial agent. It is an amino cyclitol glycoside, an aminoglycoside antibiotic, a diol, a monocarboxylic acid amide and a primary amino compound.
이름 및 식별자
- 우선 이름
- Astromicin
- IUPAC
- 2-amino-N-[(1S,2R,3R,4S,5S,6R)-4-amino-3-[(2R,3R,6S)-3-amino-6-[(1S)-1-aminoethyl]oxan-2-yl]oxy-2,5-dihydroxy-6-methoxycyclohexyl]-N-methylacetamide
- 영어명
- FORTIMICIN
- 분자식
- C17H35N5O6
- 분자량
- 405.49
이름 및 동의어
이름 더 보기
데이터베이스 식별자
- CAS
55779-06-1- PubChem CID
- 5284517
- DTXSID
DTXSID2022624- ChEMBL
CHEMBL3084803- ChEBI
CHEBI:37923- UNII
- 7JHD84H15J
- Nikkaji
- J34.182G
물성
구조 계산 물성
- XLogP
- -4.4
- 극성 표면적
- 193 Ų
- 수소 결합 공여자 수
- 6
- 수소 결합 수용자 수
- 10
- 회전 가능 결합 수
- 6
- 무거운 원자 수
- 28
- 형식 전하
- 0
- 복잡도
- 528
실험 및 물리화학적 성질
물리화학적 성질
- 녹는점
- 200 ° · >200° (dec)
- 끓는 점
- 526.82 °C · 526.82°C (rough estimate)
- 밀도
- 1.0897 · 1.0897 (rough estimate)
- 굴절률
- 1.76 · 1.7600 (estimate)
- 산도 계수 (pKa)
- 13.16 · 13.16±0.70(Predicted)
안전 및 규제
안전 데이터
- 독성
- LD50 (of the sulfate salt) in mice (mg/kg): 380 i.v.; 400 s.c. (Nara, 1977)
화학 및 산업
상·하류 제품 정보
상류 원료
공급사9 곳
추가 설명
정의ChEBI: An amino cyclitol glycoside that is L-chiro-inositol in which the hydroxy groups at positions 1, 4, and 6 are replaced by aminoacetyl)methylamino, amino, and methoxy groups, respectively, and in which the hydroxy group at posi ion 3 is converted to the corresponding 2,6-diamino-2,3,4,6,7-pentadeoxy-beta-L-lyxo-heptopyranoside. The major component of fortimicin, obtained from Micromonospora olivasterospora. It is adm nistered (as the sulfate salt) by intramuscular injection or intravenous infusion for the treatment of severe systemic infections due to sensitive Gram-negative organisms.
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