PUBCHEM ID 76971929
UNII J28HWY0T41
Preferred Term LOTILIBCIN HYDROCHLORIDE
CAS
INCHIKEY VBXUDTFBJRKXBU-JCBBIFMDSA-N
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mol2
Smiles CC(C)CCC[C@H](CC(N[C@@H](CO)C(N[C@H]([C@H](C(N)=O)O)C(N[C@@H](CO)C(NCC(N(C)[C@H](Cc1ccccc1)C(N[C@@H](CC(C)C)C(N[C@H](CCCN)C(N[C@@H](CCC(O)=O)C(N[C@H](CC(N)=O)C(N[C@H](Cc1c[nH]c2c1cccc2)C(N[C@H](CCCN)C(N(C)[C@H]1C(C)C)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)=O)OC
Total Surface Area 1191,9
Relative PSA 0,39249
TPSA 609,92
cLogS -5,346
MW 1562,78
cLogP -9,3469
H-Acceptors 38
H-Donors 19
Ro5 violations 3
Druglikeness 5,8986
DrugScore 0,353105422917489
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 -0,264
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor I Non-inhibitor
P-glycoprotein Inhibitor II Inhibitor
Renal Organic Cation Transporter Non-inhibitor
Subcellular localization Lysosome
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 Non-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 1,4681
Tetrahymena Pyriformis Toxicity I High TPT
Tetrahymena Pyriformis Toxicity II 0,4849
Tetrahymena Pyriformis Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity 3,027
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.