Cefamandole (BioDeep_00000001865)
Secondary id: BioDeep_00001868028
human metabolite blood metabolite Chemicals and Drugs Antibiotics Volatile Flavor Compounds
代谢物信息卡片
化学式: C18H18N6O5S2 (462.0780058)
中文名称: 头孢孟多, 头孢孟多锂
谱图信息:
最多检出来源 Homo sapiens(blood) 16.67%
分子结构信息
SMILES: CN1C(=NN=N1)SCC2=C(N3C(C(C3=O)NC(=O)C(C4=CC=CC=C4)O)SC2)C(=O)O
InChI: InChI=1S/C18H18N6O5S2/c1-23-18(20-21-22-23)31-8-10-7-30-16-11(15(27)24(16)12(10)17(28)29)19-14(26)13(25)9-5-3-2-4-6-9/h2-6,11,13,16,25H,7-8H2,1H3,(H,19,26)(H,28,29)/t11-,13-,16-/m1/s1
描述信息
Cefamandole is only found in individuals that have used or taken this drug. It is a broad-spectrum cephalosporin antibiotic. The clinically used form of cefamandole is the formate ester cefamandole nafate, a prodrug which is administered parenterally. Cefamandole is no longer available in the United States.Like all beta-lactam antibiotics, cefamandole binds to specific penicillin-binding proteins (PBPs) located inside the bacterial cell wall, causing the inhibition of the third and last stage of bacterial cell wall synthesis. Cell lysis is then mediated by bacterial cell wall autolytic enzymes such as autolysins; it is possible that cefamandole interferes with an autolysin inhibitor.
J - Antiinfectives for systemic use > J01 - Antibacterials for systemic use > J01D - Other beta-lactam antibacterials > J01DC - Second-generation cephalosporins
D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D002511 - Cephalosporins
D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D047090 - beta-Lactams
D000890 - Anti-Infective Agents > D000900 - Anti-Bacterial Agents > D007769 - Lactams
C254 - Anti-Infective Agent > C258 - Antibiotic > C260 - Beta-Lactam Antibiotic
同义名列表
20 个代谢物同义名
(6R,7R)-7-[(2R)-2-hydroxy-2-phenylacetamido]-3-{[(1-methyl-1H-1,2,3,4-tetrazol-5-yl)sulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; (6R,7R)-7-{[(2R)-2-hydroxy-2-phenylacetyl]amino}-3-{[(1-methyl-1H-tetrazol-5-yl)sulphanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; (6R,7R)-7-{[(2R)-2-hydroxy-2-phenylacetyl]amino}-3-{[(1-methyl-1H-tetrazol-5-yl)sulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; (6R,7R)-7-{[(2R)-2-hydroxy-2-phenylacetyl]amino}-3-{[(1-methyl-1H-tetrazol-5-yl)sulphanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate; (6R,7R)-7-{[(2R)-2-hydroxy-2-phenylacetyl]amino}-3-{[(1-methyl-1H-tetrazol-5-yl)sulfanyl]methyl}-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylate; 7-[(2-hydroxy-2-phenylacetyl)amino]-3-[(1-methyltetrazol-5-yl)sulfanylmethyl]-8-oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid; (6R,7R)-7-(R)-Mandelamido-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-carboxylic acid; (6R,7R)-7-(R)-Mandelamido-3-(((1-methyl-1H-tetrazol-5-yl)thio)methyl)-8-oxo-5-thia-1-azabicyclo(4.2.0)oct-2-ene-carboxylate; Cefamandole nafate; Compound 83405; L-Cefamandole; Cefamandolum; Cephamandole; Cefamandole; Cefamandol; Cephadole; Cefadole; CMD; Cefamandole; Cefamandole sodium
数据库引用编号
23 个数据库交叉引用编号
- ChEBI: CHEBI:3480
- KEGG: C06879
- KEGGdrug: D02344
- PubChem: 456255
- PubChem: 2614
- HMDB: HMDB0015421
- Metlin: METLIN1581
- DrugBank: DB01326
- ChEMBL: CHEMBL1146
- Wikipedia: Cefamandole
- MeSH: Cefamandole
- chemspider: 401748
- CAS: 30034-03-8
- CAS: 34444-01-4
- PMhub: MS000001327
- PubChem: 9096
- PDB-CCD: SMX
- NIKKAJI: J17.432G
- RefMet: Cefamandole
- KNApSAcK: 3480
- KEGG: C13968
- PubChem: 854209
- KNApSAcK: 34614
分类词条
相关代谢途径
Reactome(0)
BioCyc(0)
PlantCyc(0)
代谢反应
0 个相关的代谢反应过程信息。
Reactome(0)
BioCyc(0)
WikiPathways(0)
Plant Reactome(0)
INOH(0)
PlantCyc(0)
COVID-19 Disease Map(0)
PathBank(0)
PharmGKB(0)
2 个相关的物种来源信息
- 7461 - Apis cerana: 10.1371/JOURNAL.PONE.0175573
- 9606 - Homo sapiens: -
在这里通过桑基图来展示出与当前的这个代谢物在我们的BioDeep知识库中具有相关联信息的其他代谢物。在这里进行关联的信息来源主要有:
- PubMed: 来源于PubMed文献库中的文献信息,我们通过自然语言数据挖掘得到的在同一篇文献中被同时提及的相关代谢物列表,这个列表按照代谢物同时出现的文献数量降序排序,取前10个代谢物作为相关研究中关联性很高的代谢物集合展示在桑基图中。
- NCBI Taxonomy: 通过文献数据挖掘,得到的代谢物物种来源信息关联。这个关联信息同样按照出现的次数降序排序,取前10个代谢物作为高关联度的代谢物集合展示在桑吉图上。
- Chemical Taxonomy: 在物质分类上处于同一个分类集合中的其他代谢物
- Chemical Reaction: 在化学反应过程中,存在为当前代谢物相关联的生化反应过程中的反应底物或者反应产物的关联代谢物信息。
点击图上的相关代谢物的名称,可以跳转到相关代谢物的信息页面。
文献列表
- Qian Wang, Xuyang Liu, Ming Su, Zhihong Shi, Hanwen Sun. Study on the interaction characteristics of cefamandole with bovine serum albumin by spectroscopic technique.
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1988 Dec; 7(6):396-9. doi:
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The Journal of reproductive medicine.
1988 Dec; 33(12):939-44. doi:
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Orvosi hetilap.
1988 Nov; 129(47):2531-3. doi:
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Drug intelligence & clinical pharmacy.
1988 Nov; 22(11):864-8. doi:
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The Australian and New Zealand journal of surgery.
1988 Sep; 58(9):733-5. doi:
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The Journal of antimicrobial chemotherapy.
1988 Aug; 22(2):266-8. doi:
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Journal of clinical pharmacology.
1988 Jul; 28(7):655-9. doi:
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Biopharmaceutics & drug disposition.
1988 May; 9(3):251-7. doi:
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Antimicrobial agents and chemotherapy.
1988 Apr; 32(4):485-7. doi:
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Helvetica chirurgica acta.
1988 Apr; 54(6):763-70. doi:
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Clinical orthopaedics and related research.
1988 Mar; ?(228):117-22. doi:
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British medical journal (Clinical research ed.).
1988 Feb; 296(6619):433. doi:
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The Journal of pediatrics.
1988 Feb; 112(2):291-4. doi:
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Chemotherapy.
1988; 34(3):185-90. doi:
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Antimicrobial agents and chemotherapy.
1988 Jan; 32(1):128-30. doi:
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The Annals of thoracic surgery.
1988 Jan; 45(1):24-7. doi:
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Drug intelligence & clinical pharmacy.
1988 Jan; 22(1):58-61. doi:
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Archives of orthopaedic and traumatic surgery. Archiv fur orthopadische und Unfall-Chirurgie.
1988; 107(4):228-30. doi:
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Japanese journal of pharmacology.
1987 Nov; 45(3):303-15. doi:
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Orthopedics.
1987 Oct; 10(10):1405-9. doi:
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Chemioterapia : international journal of the Mediterranean Society of Chemotherapy.
1987 Apr; 6(2):95-8. doi:
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Surgery, gynecology & obstetrics.
1987 Mar; 164(3):207-12. doi:
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Antimicrobial agents and chemotherapy.
1987 Feb; 31(2):292-4. doi:
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International journal of clinical pharmacology research.
1987; 7(3):225-7. doi:
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Clinical therapeutics.
1987; 10(1):82-91. doi:
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International journal of clinical pharmacology research.
1987; 7(1):45-9. doi:
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International journal of clinical pharmacology research.
1987; 7(6):481-4. doi:
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Acta microbiologica Hungarica.
1987; 34(1):39-44. doi:
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Archives of orthopaedic and traumatic surgery. Archiv fur orthopadische und Unfall-Chirurgie.
1987; 106(3):135-9. doi:
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Orthopedics.
1986 Dec; 9(12):1657-60. doi:
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Drug intelligence & clinical pharmacy.
1986 Nov; 20(11):869-73. doi:
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Antimicrobial agents and chemotherapy.
1986 Oct; 30(4):565-9. doi:
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Zeitschrift fur Urologie und Nephrologie.
1986 Oct; 79(10):545-8. doi:
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The Journal of antimicrobial chemotherapy.
1986 Oct; 18(4):521-9. doi:
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Drugs.
1986 Sep; 32(3):222-59. doi:
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Clinical pharmacology and therapeutics.
1986 Aug; 40(2):209-18. doi:
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The Journal of antimicrobial chemotherapy.
1986 Aug; 18(2):203-11. doi:
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Biopharmaceutics & drug disposition.
1986 Jul; 7(4):335-46. doi:
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American journal of ophthalmology.
1986 Jun; 101(6):684-7. doi:
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Archives of internal medicine.
1986 Jun; 146(6):1125-8. doi:
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The Journal of infectious diseases.
1986 Jun; 153(6):1069-74. doi:
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