PUBCHEM ID 71773169
UNII 1SU114WXBX
Preferred Term REBAUDIOSIDE D
CAS 63279-13-0
INCHIKEY RPYRMTHVSUWHSV-CUZJHZIBSA-N
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mol2
Smiles C[C@@](CCC1)([C@@H](CC[C@@](C2)(C(C3)=C)O[C@H]([C@H]([C@@H]4O[C@H]([C@H]([C@@H]5O)O)O[C@@H](CO)[C@@H]5O)O[C@H]([C@H]([C@@H]5O)O)O[C@@H](CO)[C@@H]5O)O[C@@H](CO)[C@@H]4O)[C@@]23CC2)[C@@H]2[C@@]1(C)C(O[C@H]([C@H]([C@@H]1O)O[C@H]([C@H]([C@@H]2O)O)O[C@@H](CO)[
Total Surface Area 736,75
Relative PSA 0,4557
TPSA 453,28
cLogS -2,567
MW 1129,16
cLogP -5,8914
H-Acceptors 28
H-Donors 17
Ro5 violations 3
Druglikeness -9,1928
DrugScore 0,24006202606333
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 -0,671
P-glycoprotein Substrate Substrate
P-glycoprotein Inhibitor I 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 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 0,9089
Tetrahymena Pyriformis Toxicity I High TPT
Tetrahymena Pyriformis Toxicity II 0,8858
Tetrahymena Pyriformis Toxicity High HBT
Biodegradation Not ready biodegradable
Acute Oral Toxicity I
Rat Acute Toxicity 3,7314
Carcinogenicity (Three-class) Non-required
These data are only available for scientific research purposes.