1,2,5-Trihydroxy-4-(2-methylbut-3-en-2-yl)-7-(3-methylbut-1-enyl)xanthen-9-one

Details

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Internal ID 6dd3ee52-7ede-4b49-9ff0-2d04df6d9f81
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones
IUPAC Name 1,2,5-trihydroxy-4-(2-methylbut-3-en-2-yl)-7-(3-methylbut-1-enyl)xanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H24O5/c1-6-23(4,5)15-11-16(24)20(27)18-19(26)14-9-13(8-7-12(2)3)10-17(25)21(14)28-22(15)18/h6-12,24-25,27H,1H2,2-5H3
InChI Key BNMRXDRRGVXHMD-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O5
Molecular Weight 380.40 g/mol
Exact Mass 380.16237386 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 6.20
Atomic LogP (AlogP) 5.20
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 1,2,5-Trihydroxy-4-(2-methylbut-3-en-2-yl)-7-(3-methylbut-1-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 + 0.9692 96.92%
Caco-2 - 0.7202 72.02%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7061 70.61%
OATP2B1 inhibitior - 0.5679 56.79%
OATP1B1 inhibitior + 0.8530 85.30%
OATP1B3 inhibitior + 0.9832 98.32%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior + 0.7425 74.25%
P-glycoprotein inhibitior + 0.6064 60.64%
P-glycoprotein substrate - 0.7327 73.27%
CYP3A4 substrate + 0.5491 54.91%
CYP2C9 substrate - 0.6050 60.50%
CYP2D6 substrate - 0.8567 85.67%
CYP3A4 inhibition - 0.5659 56.59%
CYP2C9 inhibition - 0.7195 71.95%
CYP2C19 inhibition - 0.6393 63.93%
CYP2D6 inhibition - 0.8613 86.13%
CYP1A2 inhibition + 0.8139 81.39%
CYP2C8 inhibition - 0.5862 58.62%
CYP inhibitory promiscuity - 0.6150 61.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6116 61.16%
Eye corrosion - 0.9879 98.79%
Eye irritation - 0.5884 58.84%
Skin irritation - 0.6832 68.32%
Skin corrosion - 0.8650 86.50%
Ames mutagenesis + 0.5636 56.36%
Human Ether-a-go-go-Related Gene inhibition - 0.6058 60.58%
Micronuclear + 0.6600 66.00%
Hepatotoxicity + 0.6823 68.23%
skin sensitisation - 0.6703 67.03%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.6716 67.16%
Acute Oral Toxicity (c) III 0.6588 65.88%
Estrogen receptor binding + 0.8207 82.07%
Androgen receptor binding + 0.7794 77.94%
Thyroid receptor binding + 0.7582 75.82%
Glucocorticoid receptor binding + 0.7964 79.64%
Aromatase binding + 0.7510 75.10%
PPAR gamma + 0.8057 80.57%
Honey bee toxicity - 0.7896 78.96%
Biodegradation - 0.9000 90.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9911 99.11%

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 99.03% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 97.25% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 96.34% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 94.82% 94.73%
CHEMBL1951 P21397 Monoamine oxidase A 94.66% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.38% 89.00%
CHEMBL2581 P07339 Cathepsin D 93.72% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.47% 94.45%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.20% 90.71%
CHEMBL3192 Q9BY41 Histone deacetylase 8 85.56% 93.99%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 85.50% 99.23%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.20% 100.00%
CHEMBL4530 P00488 Coagulation factor XIII 83.95% 96.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.31% 86.33%
CHEMBL3194 P02766 Transthyretin 82.26% 90.71%
CHEMBL2964 P36507 Dual specificity mitogen-activated protein kinase kinase 2 80.34% 80.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.29% 94.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.08% 85.14%

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.
Garcinia vilersiana

Cross-Links

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PubChem 162967335
LOTUS LTS0257761
wikiData Q104938900