PUBCHEM ID 56840638
UNII AL5667FY0W
Preferred Term TYLVALOSIN TARTRATE
CAS 63428-13-7
INCHIKEY OLLSDNUHBJHKJS-XKORHJEPSA-N
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mol2
Smiles CC[C@@H]([C@H](CO[C@H]([C@H]([C@H]1OC)OC)O[C@@H](C)[C@@H]1O)/C=C(\C)/C=C/C([C@@H](C)C[C@@H](CC=O)[C@H]([C@H](C)[C@H](C1)OC(C)=O)O[C@H]([C@H]([C@@H]2N(C)C)O)O[C@@H](C)[C@@H]2O[C@H](C[C@]2(C)O)O[C@H](C)[C@H]2OC(CC(C)C)=O)=O)OC1=O
Total Surface Area 793,73
Relative PSA 0,27472
TPSA 250,81
cLogS -5,759
MW 1042,26
cLogP 4,1373
H-Acceptors 20
H-Donors 3
Ro5 violations 2
Druglikeness 6,0966
DrugScore 0,168535722488538
Mutagenic none
Tumorigenic none
Reproductive Effective none
Irritant high
Blood-Brain Barrier BBB-
Human Intestinal Absorption HIA+
Caco-2 Permeability I Caco2-
Caco-2 Permeability II 0,6585
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 Non-inhibitor
AMES Toxicity Non AMES toxic
Carcinogens Non-carcinogens
Fish Toxicity I High FHMT
Fish Toxicity II 1,0194
Tetrahymena Pyriformis Toxicity I High TPT
Tetrahymena Pyriformis Toxicity II 0,7129
Tetrahymena Pyriformis Toxicity High HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity 2,4295
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.