(3S)-5,7-dihydroxy-3-[(1R,9R,12S,14R)-5-hydroxy-9,13,13-trimethyl-8-oxatetracyclo[7.4.1.02,7.012,14]tetradeca-2(7),3,5-trien-4-yl]-6-methyl-2,3-dihydrochromen-4-one

Details

Top
Internal ID ad258d95-3ed5-4c11-bee0-da40600f5fd8
Taxonomy Phenylpropanoids and polyketides > Isoflavonoids > Isoflavans > Isoflavanones > 3-prenylated isoflavanones
IUPAC Name (3S)-5,7-dihydroxy-3-[(1R,9R,12S,14R)-5-hydroxy-9,13,13-trimethyl-8-oxatetracyclo[7.4.1.02,7.012,14]tetradeca-2(7),3,5-trien-4-yl]-6-methyl-2,3-dihydrochromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H28O6/c1-11-16(27)8-19-20(23(11)29)24(30)14(10-31-19)12-7-13-18(9-17(12)28)32-26(4)6-5-15-22(26)21(13)25(15,2)3/h7-9,14-15,21-22,27-29H,5-6,10H2,1-4H3/t14-,15+,21-,22-,26-/m1/s1
InChI Key UVHLXFVVOMQROE-CWLASNIISA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C26H28O6
Molecular Weight 436.50 g/mol
Exact Mass 436.18858861 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.77
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (3S)-5,7-dihydroxy-3-[(1R,9R,12S,14R)-5-hydroxy-9,13,13-trimethyl-8-oxatetracyclo[7.4.1.02,7.012,14]tetradeca-2(7),3,5-trien-4-yl]-6-methyl-2,3-dihydrochromen-4-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9469 94.69%
Caco-2 - 0.6629 66.29%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.7624 76.24%
OATP2B1 inhibitior - 0.8595 85.95%
OATP1B1 inhibitior + 0.8314 83.14%
OATP1B3 inhibitior + 0.9526 95.26%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.4675 46.75%
P-glycoprotein inhibitior - 0.5152 51.52%
P-glycoprotein substrate - 0.5678 56.78%
CYP3A4 substrate + 0.6899 68.99%
CYP2C9 substrate + 0.5973 59.73%
CYP2D6 substrate - 0.7917 79.17%
CYP3A4 inhibition - 0.6599 65.99%
CYP2C9 inhibition - 0.6161 61.61%
CYP2C19 inhibition - 0.6988 69.88%
CYP2D6 inhibition - 0.8802 88.02%
CYP1A2 inhibition + 0.5422 54.22%
CYP2C8 inhibition + 0.5790 57.90%
CYP inhibitory promiscuity - 0.7088 70.88%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5978 59.78%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.8774 87.74%
Skin irritation - 0.7509 75.09%
Skin corrosion - 0.9235 92.35%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7238 72.38%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.5320 53.20%
skin sensitisation - 0.8670 86.70%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.7614 76.14%
Acute Oral Toxicity (c) III 0.5700 57.00%
Estrogen receptor binding + 0.9308 93.08%
Androgen receptor binding + 0.8107 81.07%
Thyroid receptor binding + 0.7585 75.85%
Glucocorticoid receptor binding + 0.9263 92.63%
Aromatase binding + 0.7074 70.74%
PPAR gamma + 0.7155 71.55%
Honey bee toxicity - 0.7980 79.80%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9631 96.31%

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 99.12% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 95.17% 89.00%
CHEMBL2581 P07339 Cathepsin D 94.54% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 93.68% 100.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 93.44% 93.40%
CHEMBL1937 Q92769 Histone deacetylase 2 91.14% 94.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.63% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.43% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.00% 86.33%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.86% 93.99%
CHEMBL4208 P20618 Proteasome component C5 86.68% 90.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.11% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.45% 95.89%
CHEMBL1871 P10275 Androgen Receptor 84.72% 96.43%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.15% 90.71%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.36% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.87% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.58% 99.15%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 82.21% 94.78%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.86% 86.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.64% 92.62%

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.
Desmodium incanum

Cross-Links

Top
PubChem 162919357
LOTUS LTS0157021
wikiData Q105279865