PUBCHEM ID 71587124
UNII 173PDB321U
Preferred Term ENRAMYCIN B HYDROCHLORIDE
CAS 34765-98-5
INCHIKEY
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mol2
Smiles CC[C@H](C)CCCC/C=C/C=C\C(N[C@@H](CC(O)=O)C(N[C@@H]([C@@H](C)OC([C@H](c(cc1)ccc1O)NC([C@@H](C)NC([C@H](C[C@H]1NC(N)=NC1)NC(CNC([C@H](c(cc1Cl)cc(Cl)c1O)NC([C@@H](CO)NC([C@H](c(cc1)ccc1O)NC([C@@H](C[C@H]1NC(N)=NC1)NC([C@H](CCCNC(N)=O)NC([C@H]([C@H](C)O)NC([C
Total Surface Area 1749,4
Relative PSA 0,40878
TPSA 922,33
cLogS -10,113
MW 2369,36
cLogP -9,1321
H-Acceptors 57
H-Donors 34
Ro5 violations 3
Druglikeness -7,3024
DrugScore 0,125832391276558
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 0,2717
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 Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity I High FHMT
Fish Toxicity II 1,2654
Tetrahymena Pyriformis Toxicity I High TPT
Tetrahymena Pyriformis Toxicity II 0,6362
Tetrahymena Pyriformis Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity 2,7791
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.