4-(2,4-dimethylpent-3-en-2-yl)-1,6,7-trihydroxy-3-methyl-9H-xanthen-9-one

Details

Top
Internal ID 5eadda19-5c39-4c0c-b2bb-54aafd85059f
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 4-prenylated xanthones
IUPAC Name 4-(2,4-dimethylpent-3-en-2-yl)-1,6,7-trihydroxy-3-methylxanthen-9-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H22O5/c1-10(2)9-21(4,5)18-11(3)6-15(24)17-19(25)12-7-13(22)14(23)8-16(12)26-20(17)18/h6-9,22-24H,1-5H3
InChI Key BFCORSRKGHOBIS-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C21H22O5
Molecular Weight 354.40 g/mol
Exact Mass 354.14672380 g/mol
Topological Polar Surface Area (TPSA) 87.00 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.62
H-Bond Acceptor 5
H-Bond Donor 3
Rotatable Bonds 2

Synonyms

Top
BDBM50193722
4-(2,4-dimethylpent-3-en-2-yl)-1,6,7-trihydroxy-3-methyl-9H-xanthen-9-one

2D Structure

Top
2D Structure of 4-(2,4-dimethylpent-3-en-2-yl)-1,6,7-trihydroxy-3-methyl-9H-xanthen-9-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9820 98.20%
Caco-2 + 0.5198 51.98%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7457 74.57%
OATP2B1 inhibitior + 0.5760 57.60%
OATP1B1 inhibitior + 0.9415 94.15%
OATP1B3 inhibitior + 0.9859 98.59%
MATE1 inhibitior - 0.6000 60.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.5932 59.32%
P-glycoprotein inhibitior - 0.7225 72.25%
P-glycoprotein substrate - 0.7166 71.66%
CYP3A4 substrate + 0.5365 53.65%
CYP2C9 substrate - 0.6339 63.39%
CYP2D6 substrate - 0.8641 86.41%
CYP3A4 inhibition - 0.7453 74.53%
CYP2C9 inhibition + 0.6430 64.30%
CYP2C19 inhibition + 0.7675 76.75%
CYP2D6 inhibition - 0.8070 80.70%
CYP1A2 inhibition + 0.7391 73.91%
CYP2C8 inhibition - 0.7105 71.05%
CYP inhibitory promiscuity + 0.6820 68.20%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5825 58.25%
Eye corrosion - 0.9913 99.13%
Eye irritation + 0.8002 80.02%
Skin irritation - 0.6823 68.23%
Skin corrosion - 0.9261 92.61%
Ames mutagenesis + 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6636 66.36%
Micronuclear + 0.6600 66.00%
Hepatotoxicity - 0.6198 61.98%
skin sensitisation - 0.6445 64.45%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8065 80.65%
Acute Oral Toxicity (c) III 0.6879 68.79%
Estrogen receptor binding + 0.9059 90.59%
Androgen receptor binding + 0.6627 66.27%
Thyroid receptor binding + 0.7244 72.44%
Glucocorticoid receptor binding + 0.9200 92.00%
Aromatase binding + 0.7082 70.82%
PPAR gamma + 0.8704 87.04%
Honey bee toxicity - 0.8490 84.90%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.9876 98.76%

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 99.05% 91.11%
CHEMBL5966 P55899 IgG receptor FcRn large subunit p51 96.83% 90.93%
CHEMBL1951 P21397 Monoamine oxidase A 95.99% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.91% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.63% 95.56%
CHEMBL2581 P07339 Cathepsin D 94.50% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 93.90% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 90.41% 93.65%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 88.67% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 85.45% 94.00%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 84.10% 80.78%

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.
Maclura tricuspidata

Cross-Links

Top
PubChem 44419437
NPASS NPC470694
ChEMBL CHEMBL218383
LOTUS LTS0079862
wikiData Q104933946