1,3,6-Trihydroxy-2-(2-hydroxy-3-methylbut-3-enyl)-5-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one

Details

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Internal ID 307ddb70-48b4-461d-9417-624f22b008bb
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 2-prenylated xanthones
IUPAC Name 1,3,6-trihydroxy-2-(2-hydroxy-3-methylbut-3-enyl)-5-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C24H26O7/c1-11(2)6-7-13-8-15-22(29)19-18(31-23(15)24(30-5)20(13)27)10-17(26)14(21(19)28)9-16(25)12(3)4/h6,8,10,16,25-28H,3,7,9H2,1-2,4-5H3
InChI Key HBJSWNACVJQLBC-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C24H26O7
Molecular Weight 426.50 g/mol
Exact Mass 426.16785316 g/mol
Topological Polar Surface Area (TPSA) 116.00 Ų
XlogP 5.20
Atomic LogP (AlogP) 4.06
H-Bond Acceptor 7
H-Bond Donor 4
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,3,6-Trihydroxy-2-(2-hydroxy-3-methylbut-3-enyl)-5-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9826 98.26%
Caco-2 - 0.6372 63.72%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Nucleus 0.4530 45.30%
OATP2B1 inhibitior - 0.5585 55.85%
OATP1B1 inhibitior + 0.8880 88.80%
OATP1B3 inhibitior + 0.9260 92.60%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5996 59.96%
P-glycoprotein inhibitior - 0.4479 44.79%
P-glycoprotein substrate - 0.6045 60.45%
CYP3A4 substrate + 0.6152 61.52%
CYP2C9 substrate - 0.5948 59.48%
CYP2D6 substrate - 0.7986 79.86%
CYP3A4 inhibition - 0.5566 55.66%
CYP2C9 inhibition - 0.5307 53.07%
CYP2C19 inhibition + 0.7395 73.95%
CYP2D6 inhibition + 0.5392 53.92%
CYP1A2 inhibition + 0.7324 73.24%
CYP2C8 inhibition + 0.5404 54.04%
CYP inhibitory promiscuity + 0.6398 63.98%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7415 74.15%
Eye corrosion - 0.9866 98.66%
Eye irritation - 0.7387 73.87%
Skin irritation - 0.7550 75.50%
Skin corrosion - 0.9345 93.45%
Ames mutagenesis - 0.5200 52.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5677 56.77%
Micronuclear + 0.5059 50.59%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.7423 74.23%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.8957 89.57%
Acute Oral Toxicity (c) III 0.5943 59.43%
Estrogen receptor binding + 0.8798 87.98%
Androgen receptor binding + 0.5575 55.75%
Thyroid receptor binding + 0.5767 57.67%
Glucocorticoid receptor binding + 0.8250 82.50%
Aromatase binding + 0.7199 71.99%
PPAR gamma + 0.8343 83.43%
Honey bee toxicity - 0.6980 69.80%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9759 97.59%

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%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.70% 94.45%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 98.57% 85.14%
CHEMBL2581 P07339 Cathepsin D 97.86% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 97.38% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.52% 89.00%
CHEMBL3401 O75469 Pregnane X receptor 91.26% 94.73%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 90.80% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.51% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.81% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.67% 89.34%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.63% 92.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.97% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.14% 99.23%
CHEMBL3192 Q9BY41 Histone deacetylase 8 84.37% 93.99%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.47% 96.95%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 81.81% 99.15%

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.
Calophyllum brasiliense

Cross-Links

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PubChem 21635678
LOTUS LTS0155845
wikiData Q105025324