Lespecyrtin G1

Details

Top
Internal ID 8c4d3e07-e391-4096-b094-f7fd56ece2f8
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Coumestans
IUPAC Name 3,8,9-trihydroxy-10-(3-methylbut-2-enyl)-[1]benzofuro[3,2-c]chromen-6-one
SMILES (Canonical) CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)C4=C(C=C(C=C4)O)OC3=O)C
SMILES (Isomeric) CC(=CCC1=C2C(=CC(=C1O)O)C3=C(O2)C4=C(C=C(C=C4)O)OC3=O)C
InChI InChI=1S/C20H16O6/c1-9(2)3-5-12-17(23)14(22)8-13-16-19(26-18(12)13)11-6-4-10(21)7-15(11)25-20(16)24/h3-4,6-8,21-23H,5H2,1-2H3
InChI Key HGNIAVOXTWPXCX-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C20H16O6
Molecular Weight 352.30 g/mol
Exact Mass 352.09468823 g/mol
Topological Polar Surface Area (TPSA) 100.00 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.32
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
CHEMBL564378

2D Structure

Top
2D Structure of Lespecyrtin G1

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9648 96.48%
Caco-2 - 0.6196 61.96%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7787 77.87%
OATP2B1 inhibitior - 0.5547 55.47%
OATP1B1 inhibitior + 0.7812 78.12%
OATP1B3 inhibitior + 0.9435 94.35%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior + 0.7713 77.13%
P-glycoprotein inhibitior - 0.5916 59.16%
P-glycoprotein substrate - 0.5719 57.19%
CYP3A4 substrate + 0.5084 50.84%
CYP2C9 substrate - 0.5590 55.90%
CYP2D6 substrate - 0.8439 84.39%
CYP3A4 inhibition - 0.7573 75.73%
CYP2C9 inhibition + 0.8635 86.35%
CYP2C19 inhibition + 0.8099 80.99%
CYP2D6 inhibition - 0.6476 64.76%
CYP1A2 inhibition + 0.5876 58.76%
CYP2C8 inhibition + 0.4708 47.08%
CYP inhibitory promiscuity + 0.7258 72.58%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.5374 53.74%
Eye corrosion - 0.9901 99.01%
Eye irritation - 0.4857 48.57%
Skin irritation - 0.6821 68.21%
Skin corrosion - 0.9189 91.89%
Ames mutagenesis - 0.6070 60.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6906 69.06%
Micronuclear + 0.5600 56.00%
Hepatotoxicity + 0.6125 61.25%
skin sensitisation - 0.7187 71.87%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7500 75.00%
Nephrotoxicity - 0.7541 75.41%
Acute Oral Toxicity (c) III 0.3889 38.89%
Estrogen receptor binding + 0.9135 91.35%
Androgen receptor binding + 0.9194 91.94%
Thyroid receptor binding + 0.5404 54.04%
Glucocorticoid receptor binding + 0.8841 88.41%
Aromatase binding + 0.6755 67.55%
PPAR gamma + 0.8908 89.08%
Honey bee toxicity - 0.8770 87.70%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9966 99.66%

Targets

Top

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 99.59% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.61% 98.95%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 95.55% 83.57%
CHEMBL1951 P21397 Monoamine oxidase A 94.35% 91.49%
CHEMBL3401 O75469 Pregnane X receptor 93.87% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.56% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.60% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.62% 95.56%
CHEMBL3194 P02766 Transthyretin 89.52% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.74% 86.33%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.54% 94.00%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 84.84% 98.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.69% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 84.50% 99.15%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 83.55% 91.71%
CHEMBL3038469 P24941 CDK2/Cyclin A 81.52% 91.38%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.60% 99.23%

Plants that contains it

Top
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.
Lespedeza cyrtobotrya
Teucrium betonicum

Cross-Links

Top
PubChem 25208599
NPASS NPC225037
LOTUS LTS0156077
wikiData Q105027872