CID 163043481

Details

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Internal ID 981c8864-3f7c-464c-8fb2-4e704b365ef3
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name
SMILES (Canonical) CC(C)C(=O)OC1CC2(C(CCC3(O2)CC(=O)OC3)(C4C1(C5(CCC4)CO5)COC(=O)C)C)C
SMILES (Isomeric) CC(C)C(=O)OC1CC2(C(CCC3(O2)CC(=O)OC3)(C4C1(C5(CCC4)CO5)COC(=O)C)C)C
InChI InChI=1S/C26H38O8/c1-16(2)21(29)33-19-11-23(5)22(4,9-10-24(34-23)12-20(28)31-13-24)18-7-6-8-25(14-32-25)26(18,19)15-30-17(3)27/h16,18-19H,6-15H2,1-5H3
InChI Key XNHRPVTVTBEJMF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H38O8
Molecular Weight 478.60 g/mol
Exact Mass 478.25666817 g/mol
Topological Polar Surface Area (TPSA) 101.00 Ų
XlogP 2.90
Atomic LogP (AlogP) 3.34
H-Bond Acceptor 8
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 163043481

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9440 94.40%
Caco-2 - 0.5717 57.17%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8101 81.01%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8578 85.78%
OATP1B3 inhibitior + 0.9705 97.05%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.8264 82.64%
P-glycoprotein inhibitior + 0.6321 63.21%
P-glycoprotein substrate - 0.6058 60.58%
CYP3A4 substrate + 0.6740 67.40%
CYP2C9 substrate - 0.8095 80.95%
CYP2D6 substrate - 0.8590 85.90%
CYP3A4 inhibition - 0.8726 87.26%
CYP2C9 inhibition - 0.8062 80.62%
CYP2C19 inhibition - 0.7462 74.62%
CYP2D6 inhibition - 0.9345 93.45%
CYP1A2 inhibition - 0.8950 89.50%
CYP2C8 inhibition + 0.5608 56.08%
CYP inhibitory promiscuity - 0.9175 91.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5867 58.67%
Eye corrosion - 0.9839 98.39%
Eye irritation - 0.8638 86.38%
Skin irritation - 0.7557 75.57%
Skin corrosion - 0.9122 91.22%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3662 36.62%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5946 59.46%
skin sensitisation - 0.8553 85.53%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity + 0.6743 67.43%
Acute Oral Toxicity (c) III 0.4043 40.43%
Estrogen receptor binding + 0.8816 88.16%
Androgen receptor binding + 0.7167 71.67%
Thyroid receptor binding + 0.6158 61.58%
Glucocorticoid receptor binding + 0.8124 81.24%
Aromatase binding + 0.8145 81.45%
PPAR gamma + 0.7343 73.43%
Honey bee toxicity - 0.7186 71.86%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9668 96.68%

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 97.69% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.46% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.23% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.82% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.21% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.36% 97.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 92.35% 96.77%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 91.58% 92.62%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 91.03% 85.14%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.68% 89.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 89.67% 82.69%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 88.88% 95.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 88.77% 95.56%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 86.02% 91.65%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.02% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.77% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.63% 99.23%
CHEMBL340 P08684 Cytochrome P450 3A4 85.27% 91.19%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.72% 86.33%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 83.96% 89.05%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.64% 93.04%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.16% 95.17%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.44% 89.50%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.26% 97.28%

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 orientalis

Cross-Links

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PubChem 163043481
LOTUS LTS0158196
wikiData Q105331665