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      Bleomycin
 Brand Names/Synonyms
- BLM 
 - Blenoxane 
 - Bleo 
 - Bleocin 
 - Bleomicin 
 - Bleomicina [INN-Spanish] 
 - Bleomycin (USAN) 
 - Bleomycin sulfate 
 - Bleomycine [INN-French] 
 - Bleomycins 
 - Bleomycinum [INN-Latin] 
  
 Brand Name MixturesNot Available
 Chemical IUPAC Name3-[[2-[2-[2-[2-[4-[2-[6-amino-2-[1-(2-amino-2-carbamoyl-ethyl)amino-2-carbamoyl- ethyl]-5-methyl-pyrimidin-4-yl]carbonylamino-3-[3-[4-carbamoyloxy-3,5-dihydroxy- 6-(hydroxymethyl)tetrahydropyran-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl) tetrahydropyran-2-yl]oxy-3-(3H-imidazol-4-yl)propanoyl]amino-3-hydroxy- 2-methyl-pentanoyl]amino-3-hydroxy-butanoyl]aminoethyl]-1,3-thiazol-4-yl] -1,3-thiazol-4-yl]carbonylamino]propyl-dimethyl-sulfonium
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				         (µ¿¹°½ÇÇè°ú ÀÓ»ó ½ÃÇè¿¡¼ À§Ç輺 º¸°íµÊ. -Briggs G, et al. Drugs in Pregnancy and Lactation 7th edit. )
				        
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    | Mechanism of Action | 
    
       Bleomycin¿¡ ´ëÇÑ Mechanism_Of_Action Á¤º¸ Although the exact mechanism of action of bleomycin is unknown, available evidence would seem to indicate that the main mode of action is the inhibition of DNA synthesis with some evidence of lesser inhibition of RNA and protein synthesis. 
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       Bleomycin¿¡ ´ëÇÑ Pharmacology Á¤º¸ Bleomycin is an antibiotic which has been shown to have antitumor activity. Bleomycin selectively inhibits the synthesis of deoxyribonucleic acid (DNA). The guanine and cytosine content correlates with the degree of mitomycin-induced cross-linking. At high concentrations of the drug, cellular RNA and protein synthesis are also suppressed. Bleomycin has been shown in vitro to inhibit B cell, T cell, and macrophage proliferation and impair antigen presentation, as well as the secretion of interferon gamma, TNFa, and IL-2. The antibiotic antitumor drugs are cell cycle-nonspecific except for Bleomycin (which has major effects in G2 and M phases). 
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    | Metabolism | 
    
       Bleomycin¿¡ ´ëÇÑ Metabolism Á¤º¸ # Phase_1_Metabolizing_Enzyme:Cytochrome P450 1A1 (CYP1A1) 
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    | Protein Binding | 
    
       Bleomycin¿¡ ´ëÇÑ ´Ü¹é°áÇÕ Á¤º¸ 1% 
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    | Half-life | 
    
       Bleomycin¿¡ ´ëÇÑ ¹Ý°¨±â Á¤º¸ 115 minutes 
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    | Absorption | 
    
       Bleomycin¿¡ ´ëÇÑ Absorption Á¤º¸ Systemic absorption is approximately 45%. 
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       Bleomycin HClÀÇ ¾à¹°µ¿·ÂÇÐÀÚ·á 
-  ÃÖ°íÇ÷Áß³óµµ µµ´Þ½Ã±â : IM : 60ºÐ
  
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 -  ¼Ò½Ç : ½Å¹è¼³ (Ȱ¼ºÇü ´ë»çü·Î¼ 50-70 %)
 
 -  Ç÷¾×Åõ¼®À¸·Î Á¦°ÅµÇÁö ¾ÊÀ½
   
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    | Biotransformation | 
    
       Bleomycin¿¡ ´ëÇÑ Biotransformation Á¤º¸ Hepatic 
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    | Toxicity | 
    
       Bleomycin¿¡ ´ëÇÑ Toxicity Á¤º¸ Excessive exposure may cause fever, chills, nausea, vomiting, mental, confusion, and wheezing. Bleomycin may cause irritation to eyes, skin and respiratory tract. It may also cause a darkening or thickening of the skin. It may cause an allergic reaction. 
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    | Drug Interactions | 
    
       Bleomycin¿¡ ´ëÇÑ Drug_Interactions Á¤º¸ Not Available 
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    CYP450  Drug Interaction | 
    
      [CYP450 TableÁ÷Á¢Á¶È¸] 
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    | Food Interaction | 
    
       Bleomycin¿¡ ´ëÇÑ Food Interaction Á¤º¸ Not Available 
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    | Drug Target | 
    
      
      [Drug Target]
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    | SNP Á¤º¸ | 
    
      Name:Bleomycin (DB00290)
 Interacting Gene/Enzyme:Bleomycin hydrolase (Gene symbol = BLMH) Swissprot Q13867
 SNP(s):rs10500565 (A Allele)
 Effect:Improved response to bleomycin
 Reference(s):de Haas EC, Zwart N, Meijer C, Nuver J, Boezen HM, Suurmeijer AJ, Hoekstra HJ, van der Steege G, Sleijfer DT, Gietema JA: Variation in bleomycin hydrolase gene is associated with reduced survival after chemotherapy for testicular germ cell cancer. J Clin Oncol. 2008 Apr 10;26(11):1817-23. [PubMed] 
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    | Description | 
    
       Bleomycin¿¡ ´ëÇÑ Description Á¤º¸ A complex of related glycopeptide antibiotics from Streptomyces verticillus consisting of bleomycin A2 and B2. It inhibits DNA metabolism and is used as an antineoplastic, especially for solid tumors. [PubChem] 
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    | Drug Category | 
    
       Bleomycin¿¡ ´ëÇÑ Drug_Category Á¤º¸ Antibiotics, AntineoplasticAntimetabolites 
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    | Smiles String Canonical | 
    
       Bleomycin¿¡ ´ëÇÑ Smiles_String_canonical Á¤º¸ CC(O)C(NC(=O)C(C)C(O)C(C)NC(=O)C(NC(=O)C1=C(C)C(N)=NC(=N1)C(CC(N)=O)NCC(N)C(N)=O)C(OC1OC(CO)C(O)C(O)C1OC1OC(CO)C(O)C(OC(N)=O)C1O)C1=CN=CN1)C(=O)NCCC1=NC(=CS1)C1=NC(=CS1)C(=O)NCCC[S+](C)C 
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    | Smiles String Isomeric | 
    
       Bleomycin¿¡ ´ëÇÑ Smiles_String_isomeric Á¤º¸ C[C@@H](O)[C@H](NC(=O)[C@@H](C)[C@H](O)[C@@H](C)NC(=O)[C@@H](NC(=O)C1=C(C)C(N)=NC(=N1)[C@H](CC(N)=O)NC[C@H](N)C(N)=O)[C@@H](O[C@@H]1O[C@@H](CO)[C@H](O)[C@@H](O)[C@@H]1O[C@@H]1O[C@@H](CO)[C@H](O)[C@@H](OC(N)=O)[C@@H]1O)C1=CN=CN1)C(=O)NCCC1=NC(=CS1)C1=NC(=CS1)C(=O)NCCC[S+](C)C 
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    | InChI Identifier | 
    
       Bleomycin¿¡ ´ëÇÑ InChI_Identifier Á¤º¸ InChI=1/C55H83N17O21S3/c1-20-33(69-46(72-44(20)58)25(12-31(57)76)64-13-24(56)45(59)82)50(86)71-35(41(26-14-61-19-65-26)91-54-43(39(80)37(78)29(15-73)90-54)92-53-40(81)42(93-55(60)88)38(79)30(16-74)89-53)51(87)66-22(3)36(77)21(2)47(83)70-34(23(4)75)49(85)63-10-8-32-67-28(18-94-32)52-68-27(17-95-52)48(84)62-9-7-11-96(5)6/h14,17-19,21-25,29-30,34-43,53-54,64,73-75,77-81H,7-13,15-16,56H2,1-6H3,(H13-,57,58,59,60,61,62,63,65,66,69,70,71,72,76,82,83,84,85,86,87,88)/p+1/t21-,22+,23+,24-,25-,29?,30?,34-,35-,36-,37?,38?,39?,40?,41-,42?,43?,53?,54?/m0/s1/fC55H84N17O21S3/h62-63,65-66,70-71H,57-60H2/q+1 
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    | Chemical IUPAC Name | 
    
       Bleomycin¿¡ ´ëÇÑ Chemical_IUPAC_Name Á¤º¸ 3-[[2-[2-[2-[[(2S,3R)-2-[[(2S,3S,4R)-4-[[(2S,3R)-2-[[6-amino-2-[(1S)-3-amino-1-[[(2S)-2,3-diamino-3-oxopropyl]amino]-3-oxopropyl]-5-methylpyrimidine-4-carbonyl]amino]-3-[3-[4-carbamoyloxy-3,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,5-dihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-3-(3H-imidazol-4-yl)propanoyl]amino]-3-hydroxy-2-methylpentanoyl]amino]-3-hydroxybutanoyl]amino]ethyl]-1,3-thiazol-4-yl]1,3-thiazole-4-carbonyl]amino]propyl-dimethylsulfanium 
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