PUBCHEM ID 76972805
UNII JB87J72236
Preferred Term LANATOSIDE D
CAS 11030-31-2
INCHIKEY CMJNCFRBMBTRSY-WRBNHJDJSA-N
Download mol2, pdbqt
mol2
Smiles C[C@H]([C@H]([C@H](C1)O)O[C@@H](C[C@@H]2O)O[C@H](C)[C@H]2O[C@@H](C[C@@H]2OC(C)=O)O[C@H](C)[C@H]2O[C@@H]([C@@H]([C@H]2O)O)O[C@H](CO)[C@H]2O)O[C@H]1O[C@@H](CC1)C[C@@H](CC2)[C@@]1(C)[C@@H](C[C@H]([C@]1(C)[C@H]([C@H](C3)O)C(CO4)=CC4=O)O)[C@@H]2[C@]13O
Total Surface Area 679,27
Relative PSA 0,35918
TPSA 308,51
cLogS -5,398
MW 1001,12
cLogP -0,3092
H-Acceptors 21
H-Donors 9
Ro5 violations 3
Druglikeness -0,99515
DrugScore 0,222510400809831
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 -0,6853
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor I Inhibitor
P-glycoprotein Inhibitor II 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 1,0238
Tetrahymena Pyriformis Toxicity I High TPT
Tetrahymena Pyriformis Toxicity II 0,9307
Tetrahymena Pyriformis Toxicity High HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity I
Rat Acute Toxicity 5,0099
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.