PUBCHEM ID 121494086
UNII JD0HM3LMNW
Preferred Term BLEOMYCIN B2 HYDROCHLORIDE
CAS 55658-44-1
INCHIKEY ZNLSDKREHVABLV-WEJIAYKGSA-N
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mol2
Smiles C[C@H]([C@H]([C@H](C)NC([C@@H]([C@@H](c1cnc[nH]1)O[C@H]([C@@H]([C@@H]1O)O[C@@H]([C@@H]([C@@H]2OC(N)=O)O)O[C@@H](CO)[C@@H]2O)O[C@H](CO)[C@@H]1O)NC(c1nc([C@@H](CC(N)=O)NC[C@H](C(N)=O)N)nc(N)c1C)=O)=O)O)C(N[C@H]([C@H](C)O)C(NCCc1nc(-c2nc(C(NCCCCN=C(N)N)=O)cs
Total Surface Area 1019,1
Relative PSA 0,54542
TPSA 747,95
cLogS -2,065
MW 1425,52
cLogP -11,204
H-Acceptors 41
H-Donors 22
Ro5 violations 3
Druglikeness 4,4188
DrugScore 0,484493455534026
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant none
Blood-Brain Barrier BBB-
Human Intestinal Absorption HIA-
Caco-2 Permeability I Caco2-
Caco-2 Permeability II -0,1297
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor I Non-inhibitor
P-glycoprotein Inhibitor II Non-inhibitor
Renal Organic Cation Transporter Non-inhibitor
Subcellular localization Mitochondria
CYP450 2C9 Substrate Non-substrate
CYP450 2D6 Substrate Non-substrate
CYP450 3A4 Substrate Substrate
CYP450 1A2 Inhibitor Non-inhibitor
CYP450 2C9 Inhibitor Non-inhibitor
CYP450 2D6 Inhibitor Non-inhibitor
CYP450 2C19 Inhibitor Non-inhibitor
CYP450 3A4 Inhibitor Inhibitor
CYP Inhibitory Promiscuity Low CYP Inhibitory Promiscuity
Human Ether-a-go-go-Related Gene Inhibition I Weak inhibitor
Human Ether-a-go-go-Related Gene Inhibition II Inhibitor
AMES Toxicity AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity I High FHMT
Fish Toxicity II 1,4604
Tetrahymena Pyriformis Toxicity I High TPT
Tetrahymena Pyriformis Toxicity II 0,5226
Tetrahymena Pyriformis Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity 2,5708
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.