CID 163086450

Details

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Internal ID b7b962c6-13fa-4a98-995a-f1d43693e542
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name
SMILES (Canonical) CC(=O)OCC12C(CCCC13CO3)C4(C(CC5(CC(=O)OC5)OC4(CC2OC(=O)C6=CC=CC=C6)C)OC(=O)C)C
SMILES (Isomeric) CC(=O)OCC12C(CCCC13CO3)C4(C(CC5(CC(=O)OC5)OC4(CC2OC(=O)C6=CC=CC=C6)C)OC(=O)C)C
InChI InChI=1S/C31H38O10/c1-19(32)36-18-31-22(11-8-12-30(31)17-38-30)28(4)23(39-20(2)33)14-29(15-25(34)37-16-29)41-27(28,3)13-24(31)40-26(35)21-9-6-5-7-10-21/h5-7,9-10,22-24H,8,11-18H2,1-4H3
InChI Key LSFZDBKRSZASHD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C31H38O10
Molecular Weight 570.60 g/mol
Exact Mass 570.24649740 g/mol
Topological Polar Surface Area (TPSA) 127.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 3.54
H-Bond Acceptor 10
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 163086450

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9545 95.45%
Caco-2 - 0.7272 72.72%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.7806 78.06%
OATP2B1 inhibitior - 0.8623 86.23%
OATP1B1 inhibitior + 0.8393 83.93%
OATP1B3 inhibitior + 0.9637 96.37%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6000 60.00%
BSEP inhibitior + 0.9649 96.49%
P-glycoprotein inhibitior + 0.8348 83.48%
P-glycoprotein substrate - 0.5164 51.64%
CYP3A4 substrate + 0.6897 68.97%
CYP2C9 substrate - 0.8166 81.66%
CYP2D6 substrate - 0.8628 86.28%
CYP3A4 inhibition - 0.6896 68.96%
CYP2C9 inhibition - 0.8413 84.13%
CYP2C19 inhibition - 0.7036 70.36%
CYP2D6 inhibition - 0.9315 93.15%
CYP1A2 inhibition - 0.8432 84.32%
CYP2C8 inhibition + 0.7979 79.79%
CYP inhibitory promiscuity - 0.8432 84.32%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5656 56.56%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.9126 91.26%
Skin irritation - 0.7559 75.59%
Skin corrosion - 0.9331 93.31%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8334 83.34%
Micronuclear - 0.6700 67.00%
Hepatotoxicity - 0.5851 58.51%
skin sensitisation - 0.8833 88.33%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.7222 72.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity + 0.6816 68.16%
Acute Oral Toxicity (c) I 0.3636 36.36%
Estrogen receptor binding + 0.8619 86.19%
Androgen receptor binding + 0.7252 72.52%
Thyroid receptor binding + 0.5496 54.96%
Glucocorticoid receptor binding + 0.8157 81.57%
Aromatase binding + 0.7599 75.99%
PPAR gamma + 0.6552 65.52%
Honey bee toxicity - 0.7913 79.13%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9818 98.18%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.79% 86.33%
CHEMBL2581 P07339 Cathepsin D 95.62% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.22% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.96% 95.56%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 92.04% 82.69%
CHEMBL221 P23219 Cyclooxygenase-1 91.92% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.43% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.94% 97.09%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 90.38% 91.65%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.74% 91.11%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 88.15% 94.62%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 87.74% 83.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.37% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.49% 89.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.24% 93.04%
CHEMBL5028 O14672 ADAM10 86.01% 97.50%
CHEMBL2535 P11166 Glucose transporter 83.13% 98.75%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.29% 92.62%
CHEMBL340 P08684 Cytochrome P450 3A4 81.42% 91.19%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.29% 100.00%

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 163086450
LOTUS LTS0136232
wikiData Q105219505