PUBCHEM ID 73350610
UNII 390H5GUO40
Preferred Term .MU.-CONOTOXIN K IIIA
CAS 884469-67-4
INCHIKEY
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mol2
Smiles NCCCC[C@@H](C(N[C@@H](Cc1c[nH]c2c1cccc2)C(N[C@@H](CSSC[C@@H](C(N[C@@H](CSSC[C@@H](C(N[C@@H](CSSC[C@@H](C(N[C@@H](CO)C(N[C@H]1CO)=O)=O)NC([C@H](CC(N)=O)N2)=O)C(N)=O)=O)NC([C@H](CCCNC(N)=N)NC([C@H](CO)NC([C@H](Cc3cnc[nH]3)NC([C@H](CC(O)=O)NC([C@H](CCCNC(N)=
Total Surface Area 1357,9
Relative PSA 0,55133
TPSA 992,78
cLogS -4,765
MW 1884,18
cLogP -16,877
H-Acceptors 50
H-Donors 31
Ro5 violations 3
Druglikeness 4,3415
DrugScore 0,387117053014921
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 -0,8944
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 Non-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 1,7345
Tetrahymena Pyriformis Toxicity I High TPT
Tetrahymena Pyriformis Toxicity II 0,3401
Tetrahymena Pyriformis Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity 2,5863
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.