2-[(8aS,10aR)-4-hydroxy-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5H-xanthen-1-yl]-3,5,7-trihydroxychromen-4-one

Details

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Internal ID 776000e1-8742-4292-8082-1aaaa69ab7ad
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 2-prenylated flavones
IUPAC Name 2-[(8aS,10aR)-4-hydroxy-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5H-xanthen-1-yl]-3,5,7-trihydroxychromen-4-one
SMILES (Canonical) CC1(CCCC2(C1CC3=C(C=CC(=C3O2)O)C4=C(C(=O)C5=C(C=C(C=C5O4)O)O)O)C)C
SMILES (Isomeric) C[C@@]12CCCC([C@@H]1CC3=C(C=CC(=C3O2)O)C4=C(C(=O)C5=C(C=C(C=C5O4)O)O)O)(C)C
InChI InChI=1S/C25H26O7/c1-24(2)7-4-8-25(3)18(24)11-14-13(5-6-15(27)22(14)32-25)23-21(30)20(29)19-16(28)9-12(26)10-17(19)31-23/h5-6,9-10,18,26-28,30H,4,7-8,11H2,1-3H3/t18-,25+/m0/s1
InChI Key RQGIPLQXOXXTRU-AVRWGWEMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H26O7
Molecular Weight 438.50 g/mol
Exact Mass 438.16785316 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.80
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-[(8aS,10aR)-4-hydroxy-8,8,10a-trimethyl-6,7,8a,9-tetrahydro-5H-xanthen-1-yl]-3,5,7-trihydroxychromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9416 94.16%
Caco-2 - 0.6595 65.95%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.7848 78.48%
OATP2B1 inhibitior - 0.6933 69.33%
OATP1B1 inhibitior + 0.7398 73.98%
OATP1B3 inhibitior + 0.9488 94.88%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.5981 59.81%
P-glycoprotein inhibitior + 0.5770 57.70%
P-glycoprotein substrate + 0.5422 54.22%
CYP3A4 substrate + 0.6799 67.99%
CYP2C9 substrate - 0.5681 56.81%
CYP2D6 substrate - 0.8119 81.19%
CYP3A4 inhibition - 0.6822 68.22%
CYP2C9 inhibition - 0.8424 84.24%
CYP2C19 inhibition - 0.8511 85.11%
CYP2D6 inhibition - 0.9161 91.61%
CYP1A2 inhibition + 0.5688 56.88%
CYP2C8 inhibition + 0.8676 86.76%
CYP inhibitory promiscuity - 0.8153 81.53%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6908 69.08%
Eye corrosion - 0.9918 99.18%
Eye irritation - 0.7159 71.59%
Skin irritation - 0.7227 72.27%
Skin corrosion - 0.9349 93.49%
Ames mutagenesis + 0.6163 61.63%
Human Ether-a-go-go-Related Gene inhibition - 0.4938 49.38%
Micronuclear - 0.7600 76.00%
Hepatotoxicity - 0.7250 72.50%
skin sensitisation - 0.8874 88.74%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.7902 79.02%
Acute Oral Toxicity (c) III 0.6044 60.44%
Estrogen receptor binding + 0.8677 86.77%
Androgen receptor binding + 0.7612 76.12%
Thyroid receptor binding + 0.5844 58.44%
Glucocorticoid receptor binding + 0.8882 88.82%
Aromatase binding + 0.8030 80.30%
PPAR gamma + 0.8683 86.83%
Honey bee toxicity - 0.8730 87.30%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9880 98.80%

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 99.73% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 99.70% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 97.01% 89.00%
CHEMBL2581 P07339 Cathepsin D 96.35% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.94% 95.56%
CHEMBL1929 P47989 Xanthine dehydrogenase 93.25% 96.12%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.17% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.92% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 88.53% 95.89%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 86.99% 85.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.42% 100.00%
CHEMBL4208 P20618 Proteasome component C5 86.13% 90.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 85.77% 93.40%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 85.77% 90.71%
CHEMBL242 Q92731 Estrogen receptor beta 85.57% 98.35%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.34% 99.23%
CHEMBL3194 P02766 Transthyretin 85.23% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 84.78% 94.00%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 83.67% 94.42%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 82.31% 99.15%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.38% 92.94%
CHEMBL3401 O75469 Pregnane X receptor 81.26% 94.73%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 80.02% 95.64%

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.
Helminthostachys zeylanica

Cross-Links

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PubChem 162944089
LOTUS LTS0189065
wikiData Q105243313