PUBCHEM ID 91618002
UNII 17E01H280E
Preferred Term TERMINOLOSIDE
CAS 125265-68-1
INCHIKEY NNWMHSNRRWMMBI-PJISEHJASA-N
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mol2
Smiles C[C@@H]([C@@H]([C@H]([C@H]1O)O)O)O[C@H]1O[C@H]([C@@H](CO)O[C@H]([C@@H]1O)OC[C@H]([C@H]([C@@H]([C@H]2O)O)O)O[C@H]2OC([C@]2(CCC(C)(C)C3)[C@@H]3C3=CC[C@H]([C@@](C)(C[C@H]4O)[C@@H]([C@@H](C5)O)[C@](C)(CO)[C@H]4O)[C@]5(C)[C@]3(C)CC2)=O)[C@@H]1O
Total Surface Area 652,65
Relative PSA 0,37285
TPSA 335,44
cLogS -4,43
MW 975,127
cLogP -1,1512
H-Acceptors 20
H-Donors 13
Ro5 violations 3
Druglikeness -12,343
DrugScore 0,205309864049189
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 -0,2212
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor I 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 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 1,2252
Tetrahymena Pyriformis Toxicity I High TPT
Tetrahymena Pyriformis Toxicity II 0,9746
Tetrahymena Pyriformis Toxicity High HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity 3,0757
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.