CID 163002683

Details

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Internal ID 130b5255-e68e-4fd2-9063-7207a6da9b25
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name
SMILES (Canonical) CC(=O)OCC12C(CCCC13CO3)C4(CCC5(CC(=O)OC5)OC4(C(C2OC(=O)C)OC(=O)C)C)C
SMILES (Isomeric) CC(=O)OCC12C(CCCC13CO3)C4(CCC5(CC(=O)OC5)OC4(C(C2OC(=O)C)OC(=O)C)C)C
InChI InChI=1S/C26H36O10/c1-15(27)31-14-26-18(7-6-8-25(26)13-33-25)22(4)9-10-24(11-19(30)32-12-24)36-23(22,5)20(34-16(2)28)21(26)35-17(3)29/h18,20-21H,6-14H2,1-5H3
InChI Key VQKBYMQKRVMNCA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H36O10
Molecular Weight 508.60 g/mol
Exact Mass 508.23084734 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP 1.40
Atomic LogP (AlogP) 2.24
H-Bond Acceptor 10
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 163002683

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9387 93.87%
Caco-2 - 0.6140 61.40%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7797 77.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8299 82.99%
OATP1B3 inhibitior + 0.9739 97.39%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior + 0.9326 93.26%
P-glycoprotein inhibitior + 0.7470 74.70%
P-glycoprotein substrate - 0.7145 71.45%
CYP3A4 substrate + 0.6600 66.00%
CYP2C9 substrate - 0.8095 80.95%
CYP2D6 substrate - 0.8590 85.90%
CYP3A4 inhibition - 0.8760 87.60%
CYP2C9 inhibition - 0.8761 87.61%
CYP2C19 inhibition - 0.7975 79.75%
CYP2D6 inhibition - 0.9439 94.39%
CYP1A2 inhibition - 0.8825 88.25%
CYP2C8 inhibition + 0.6113 61.13%
CYP inhibitory promiscuity - 0.9048 90.48%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5882 58.82%
Eye corrosion - 0.9844 98.44%
Eye irritation - 0.8844 88.44%
Skin irritation - 0.7199 71.99%
Skin corrosion - 0.9101 91.01%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7191 71.91%
Micronuclear - 0.6400 64.00%
Hepatotoxicity - 0.6724 67.24%
skin sensitisation - 0.8895 88.95%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.6480 64.80%
Acute Oral Toxicity (c) I 0.3804 38.04%
Estrogen receptor binding + 0.8742 87.42%
Androgen receptor binding + 0.7078 70.78%
Thyroid receptor binding + 0.5683 56.83%
Glucocorticoid receptor binding + 0.7941 79.41%
Aromatase binding + 0.7800 78.00%
PPAR gamma + 0.7233 72.33%
Honey bee toxicity - 0.7458 74.58%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5950 59.50%
Fish aquatic toxicity + 0.9553 95.53%

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 97.10% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.64% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.79% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.31% 94.45%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.39% 96.77%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.07% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.95% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.72% 85.14%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.17% 95.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.74% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.94% 82.69%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 87.88% 91.65%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.19% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.78% 86.33%
CHEMBL340 P08684 Cytochrome P450 3A4 85.55% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.85% 100.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.32% 92.62%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.01% 95.89%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.80% 97.28%
CHEMBL5255 O00206 Toll-like receptor 4 81.55% 92.50%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 80.17% 93.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Scutellaria alpina

Cross-Links

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PubChem 163002683
LOTUS LTS0271407
wikiData Q105291331