PUBCHEM ID 91864495
UNII 17ZS80333G
Preferred Term SOLNATIDE
CAS 259206-53-6
INCHIKEY
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mol2
Smiles C[C@H]([C@@H](C(N(CCC1)[C@@H]1C(N[C@@H](CCC(O)=O)C(NCC(N[C@@H](C)C(N[C@@H](CCC(O)=O)C(N[C@@H](C)C(N[C@@H](CCCCN)C(N(CCC1)[C@@H]1C(N[C@@H](Cc1c[nH]c2c1cccc2)C(N[C@@H](Cc(cc1)ccc1O)C(N[C@@H](CSSC[C@@H](C(NCC(N[C@@H](CCC(N)=O)C(N[C@@H](CCCNC(N)=N)C(N[C@H]1CC
Total Surface Area 1417,7
Relative PSA 0,46349
TPSA 861,1
cLogS -5,503
MW 1923,11
cLogP -12,947
H-Acceptors 50
H-Donors 27
Ro5 violations 3
Druglikeness -1,6569
DrugScore 0,199671953720284
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 -0,6172
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 1,4449
Tetrahymena Pyriformis Toxicity I High TPT
Tetrahymena Pyriformis Toxicity II 0,449
Tetrahymena Pyriformis Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity 2,8107
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.