基本信息
- 标准SMILES
CC1=C\[C@@H](O)CC(=O)Cc2nc(co2)C(=O)N2CCC=C2C(=O)O[C@H](C(C)C)[C@H](C)/C=C/C(=O)NC\C=C\1- InChIKey
DAIKHDNSXMZDCU-FQTGFAPKSA-N- 分子式
- C28H35N3O7
- 平均分子量
- 525.6 g/mol
- 单同位素质量
- 525.24750046
概述
Pristinamycin IIA is a macrolide that is (together with pristinamycin IA) a component of pristinamycin, an oral streptogramin antibiotic produced by Streptomyces pristinaespiralis. Pristinamycin exhibits bactericidal activity against Gram positive organisms including methicillin-resistant Staphylococcus aureus. It has a role as a Mycoplasma genitalium metabolite and an antibacterial drug. It is a secondary carboxamide, a tertiary carboxamide, a pyrroline, a lactam, a macrolide antibiotic, a macrolide, a secondary alcohol, a cyclic ketone, a member of 1,3-oxazoles and an enamide.
名称与标识
- 首选名称
- Virginiamycin M1
- IUPAC
- (10R,11R,12E,17E,19E,21S)-21-hydroxy-11,19-dimethyl-10-propan-2-yl-9,26-dioxa-3,15,28-triazatricyclo[23.2.1.03,7]octacosa-1(27),6,12,17,19,25(28)-hexaene-2,8,14,23-tetrone
- 中文名
- 维吉尼亚霉素M1
- 英文名
- VIRGINIAMYCIN M1
- 分子式
- C28H35N3O7
- 分子量
- 525.59
名称与别名
展开更多名称
数据库标识
- CAS
21411-53-0- PubChem CID
- 5459319
- DTXSID
DTXSID30873800- ChEMBL
CHEMBL1236670- ChEBI
CHEBI:9997- UNII
- 8W4UOL59AZ
- EC Number
- 244-376-6
性质
结构计算性质
- XLogP
- 2.5
- 极性表面积
- 139 Ų
- 氢键供体
- 2
- 氢键受体
- 8
- 可旋转键
- 1
- 重原子
- 38
- 形式电荷
- 0
- 复杂度
- 1,030
实验与物化性质
物理化学性质
- 熔点
- 165 · 165-167℃
- 比旋光度
- 20 · D20 -218° ( c = 0.34 in ethanol)
- 沸点
- 825.2 · 825.2±65.0 °C(Predicted)
- 密度
- 1.26 · 1.26±0.1 g/cm3(Predicted)
- 储存条件
- 2 · 2-8°C
- 溶解度
- 10 mg/mL · chloroform/methanol: soluble10mg/mL
- 酸度系数(pKa)
- 13.18 · 13.18±0.70(Predicted)
- 形态
- powder
- 颜色
- yellow to tan
- 稳定性
- Light Sensitive
- InChIKey
- DAIKHDNSXMZDCU-QHKJSJJMSA-N
- SMILES
- CC(C)[C@H]1OC(=O)C2=CCCN2C(=O)c3coc(CC(=O)C[C@H](O)C=C(C)C=CCNC(=O)C=C[C@H]1C)n3
安全与法规
安全数据
- wgk
- 3
- 存储类别
- 11 - Combustible Solids
- 海关编码
- 29419090
化学与工业
药理信息
Mechanism of Action
Virginiamycin M1 is a macrocyclic lactone antibiotic that acts syngeristically with the structurally unrelated cyclic depsipeptides more commonly known as the virginiamycins B (ostreogrycin B or streptogramin B) and S to inhibit peptide elongation. This is achieved by blocking formation of a peptide bond between the growing peptide chain (peptidyl-tRNA) linked to the 50S ribosome and aminoacyl-tRNA. Virginiamycin M1 has proven to be highly active against Gram positive bacteria, particularly methicillin-resistant S. aureus.
试剂价格
- HY-N6686 · 1 mg
- 维吉尼亚霉素M1Virginiamycin M1 — 920元
- HY-N6686 · 5mg
- 维吉尼亚霉素M1Virginiamycin M1 — 2022元
供应商50 家
相关反应
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