PUBCHEM ID 56843427
UNII 0C5T02KI0E
Preferred Term .MU.-CONOTOXIN G IIIA
CAS 129129-65-3
INCHIKEY
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mol2
Smiles C[C@H]([C@@H](C(N(C[C@@H](C1)O)[C@@H]1C(N(C[C@@H](C1)O)[C@@H]1C(N[C@@H](CCCCN)C(N[C@@H](CCCCN)C(N[C@@H](CSSC[C@@H](C(N[C@@H](C)C(N)=O)=O)NC([C@H](CSSC[C@@H]1NC([C@H](CSSC[C@@H](C(N[C@@H](CCCCN)C(N(C[C@@H](C2)O)[C@@H]2C(N[C@@H](CCC(N)=O)C(N[C@H]2CCCNC(N)=N
Total Surface Area 1904,4
Relative PSA 0,51913
TPSA 1337,1
cLogS -5,261
MW 2609,08
cLogP -26,323
H-Acceptors 70
H-Donors 41
Ro5 violations 3
Druglikeness -0,92266
DrugScore 0,23041108134953
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 -0,7405
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 Low FHMT
Fish Toxicity II 1,8007
Tetrahymena Pyriformis Toxicity I High TPT
Tetrahymena Pyriformis Toxicity II 0,2483
Tetrahymena Pyriformis Toxicity Low HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity III
Rat Acute Toxicity 2,7782
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.