CID 162925161

Details

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Internal ID 7dac6091-2c05-4f5f-82ee-65cb7b7afdd4
Taxonomy Organoheterocyclic compounds > Naphthopyrans
IUPAC Name
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H38O9/c1-6-16(2)22(31)35-20-11-23(4)24(5,19(29)10-25(36-23)12-21(30)33-13-25)18-8-7-9-26(14-34-26)27(18,20)15-32-17(3)28/h6,18-20,29H,7-15H2,1-5H3
InChI Key GLMSILQFAKZQCG-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H38O9
Molecular Weight 506.60 g/mol
Exact Mass 506.25158279 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.62
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of CID 162925161

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9409 94.09%
Caco-2 - 0.6237 62.37%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8153 81.53%
OATP2B1 inhibitior - 0.8620 86.20%
OATP1B1 inhibitior + 0.8501 85.01%
OATP1B3 inhibitior + 0.9518 95.18%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5771 57.71%
BSEP inhibitior + 0.9481 94.81%
P-glycoprotein inhibitior + 0.6651 66.51%
P-glycoprotein substrate - 0.5297 52.97%
CYP3A4 substrate + 0.6953 69.53%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8910 89.10%
CYP3A4 inhibition - 0.7599 75.99%
CYP2C9 inhibition - 0.8659 86.59%
CYP2C19 inhibition - 0.8954 89.54%
CYP2D6 inhibition - 0.9328 93.28%
CYP1A2 inhibition - 0.8680 86.80%
CYP2C8 inhibition + 0.5901 59.01%
CYP inhibitory promiscuity - 0.9309 93.09%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.4908 49.08%
Eye corrosion - 0.9890 98.90%
Eye irritation - 0.9043 90.43%
Skin irritation + 0.5513 55.13%
Skin corrosion - 0.9301 93.01%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6808 68.08%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.6627 66.27%
skin sensitisation - 0.8857 88.57%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity + 0.7243 72.43%
Acute Oral Toxicity (c) I 0.8062 80.62%
Estrogen receptor binding + 0.8707 87.07%
Androgen receptor binding + 0.7007 70.07%
Thyroid receptor binding + 0.5584 55.84%
Glucocorticoid receptor binding + 0.8381 83.81%
Aromatase binding + 0.8199 81.99%
PPAR gamma + 0.6835 68.35%
Honey bee toxicity - 0.7169 71.69%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity + 0.9713 97.13%

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 94.60% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.34% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.69% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.14% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.90% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.68% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.64% 98.95%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 90.33% 82.69%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.30% 100.00%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 90.00% 96.77%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.16% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.37% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.27% 99.23%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.29% 92.94%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.56% 92.62%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.99% 93.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.70% 93.04%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.16% 97.25%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.10% 91.07%
CHEMBL340 P08684 Cytochrome P450 3A4 81.37% 91.19%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 81.18% 95.71%
CHEMBL2782 P35610 Acyl coenzyme A:cholesterol acyltransferase 1 80.56% 91.65%
CHEMBL1871 P10275 Androgen Receptor 80.19% 96.43%

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 162925161
LOTUS LTS0046766
wikiData Q105011090