pterosin C 3-O-glucoside

Details

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Internal ID 69c9bd9d-c067-44d7-a53b-a9532e74322d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (2S,3S)-3-hydroxy-2,5,7-trimethyl-6-[2-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyethyl]-2,3-dihydroinden-1-one
SMILES (Canonical) CC1C(C2=C(C1=O)C(=C(C(=C2)C)CCOC3C(C(C(C(O3)CO)O)O)O)C)O
SMILES (Isomeric) C[C@H]1[C@@H](C2=C(C1=O)C(=C(C(=C2)C)CCO[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)C)O
InChI InChI=1S/C20H28O8/c1-8-6-12-14(16(23)10(3)15(12)22)9(2)11(8)4-5-27-20-19(26)18(25)17(24)13(7-21)28-20/h6,10,13,15,17-22,24-26H,4-5,7H2,1-3H3/t10-,13+,15-,17+,18-,19+,20+/m0/s1
InChI Key VKDMMOFAMUXTQZ-VTNBQNSRSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C20H28O8
Molecular Weight 396.40 g/mol
Exact Mass 396.17841785 g/mol
Topological Polar Surface Area (TPSA) 137.00 Ų
XlogP -0.20
Atomic LogP (AlogP) -0.47
H-Bond Acceptor 8
H-Bond Donor 5
Rotatable Bonds 5

Synonyms

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pterosin C 3-O-glucoside
MLS002473106
CHEMBL1892637
HMS2196F17
AKOS040733991
NCGC00247488-01
SMR001397208

2D Structure

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2D Structure of pterosin C 3-O-glucoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5000 50.00%
Caco-2 - 0.7634 76.34%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7429 74.29%
Subcellular localzation Mitochondria 0.7054 70.54%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8125 81.25%
OATP1B3 inhibitior + 0.9321 93.21%
MATE1 inhibitior - 0.9412 94.12%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7570 75.70%
P-glycoprotein inhibitior - 0.8134 81.34%
P-glycoprotein substrate - 0.8347 83.47%
CYP3A4 substrate + 0.5755 57.55%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8569 85.69%
CYP3A4 inhibition - 0.9274 92.74%
CYP2C9 inhibition - 0.8416 84.16%
CYP2C19 inhibition - 0.8457 84.57%
CYP2D6 inhibition - 0.9386 93.86%
CYP1A2 inhibition - 0.6457 64.57%
CYP2C8 inhibition - 0.6102 61.02%
CYP inhibitory promiscuity - 0.8264 82.64%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7455 74.55%
Eye corrosion - 0.9921 99.21%
Eye irritation - 0.9411 94.11%
Skin irritation - 0.7932 79.32%
Skin corrosion - 0.9534 95.34%
Ames mutagenesis - 0.6854 68.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5865 58.65%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.6824 68.24%
skin sensitisation - 0.9037 90.37%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6563 65.63%
Acute Oral Toxicity (c) III 0.6190 61.90%
Estrogen receptor binding + 0.5824 58.24%
Androgen receptor binding - 0.5440 54.40%
Thyroid receptor binding + 0.6263 62.63%
Glucocorticoid receptor binding - 0.4730 47.30%
Aromatase binding - 0.5976 59.76%
PPAR gamma - 0.6648 66.48%
Honey bee toxicity - 0.8421 84.21%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6500 65.00%
Fish aquatic toxicity + 0.6883 68.83%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.21% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.27% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 92.80% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.62% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.98% 89.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.33% 86.92%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.58% 99.17%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.37% 96.21%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.01% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.88% 95.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.54% 90.71%

Cross-Links

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PubChem 44201982
NPASS NPC156393