Kuwanon T

Details

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Internal ID 597771df-eeb5-435b-afb4-2687c1adef3d
Taxonomy Phenylpropanoids and polyketides > Flavonoids > Flavones > 3-prenylated flavones
IUPAC Name 2-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-3-(3-methylbut-2-enyl)chromen-4-one
SMILES (Canonical) CC(=CCC1=C(C=CC(=C1O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)CC=C(C)C)O)C
SMILES (Isomeric) CC(=CCC1=C(C=CC(=C1O)C2=C(C(=O)C3=C(C=C(C=C3O2)O)O)CC=C(C)C)O)C
InChI InChI=1S/C25H26O6/c1-13(2)5-7-16-19(27)10-9-17(23(16)29)25-18(8-6-14(3)4)24(30)22-20(28)11-15(26)12-21(22)31-25/h5-6,9-12,26-29H,7-8H2,1-4H3
InChI Key KATQHJZHAFCFAQ-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C25H26O6
Molecular Weight 422.50 g/mol
Exact Mass 422.17293854 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 5.50
Atomic LogP (AlogP) 5.30
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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100187-66-4
2-[2,4-dihydroxy-3-(3-methylbut-2-enyl)phenyl]-5,7-dihydroxy-3-(3-methylbut-2-enyl)chromen-4-one
HY-N10375
LMPK12110896
CS-0498838
D85106

2D Structure

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2D Structure of Kuwanon T

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9916 99.16%
Caco-2 - 0.5337 53.37%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.7312 73.12%
OATP2B1 inhibitior + 0.5789 57.89%
OATP1B1 inhibitior + 0.7316 73.16%
OATP1B3 inhibitior + 0.8971 89.71%
MATE1 inhibitior - 0.7400 74.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.9521 95.21%
P-glycoprotein inhibitior + 0.6190 61.90%
P-glycoprotein substrate - 0.6005 60.05%
CYP3A4 substrate + 0.5742 57.42%
CYP2C9 substrate - 0.5755 57.55%
CYP2D6 substrate - 0.8328 83.28%
CYP3A4 inhibition - 0.6240 62.40%
CYP2C9 inhibition + 0.9192 91.92%
CYP2C19 inhibition + 0.9276 92.76%
CYP2D6 inhibition - 0.7701 77.01%
CYP1A2 inhibition + 0.9040 90.40%
CYP2C8 inhibition + 0.6820 68.20%
CYP inhibitory promiscuity + 0.9389 93.89%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6761 67.61%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.5422 54.22%
Skin irritation - 0.7236 72.36%
Skin corrosion - 0.9390 93.90%
Ames mutagenesis + 0.6563 65.63%
Human Ether-a-go-go-Related Gene inhibition - 0.3724 37.24%
Micronuclear + 0.5100 51.00%
Hepatotoxicity + 0.5178 51.78%
skin sensitisation - 0.7381 73.81%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity - 0.7710 77.10%
Acute Oral Toxicity (c) III 0.6621 66.21%
Estrogen receptor binding + 0.9385 93.85%
Androgen receptor binding + 0.8738 87.38%
Thyroid receptor binding + 0.5969 59.69%
Glucocorticoid receptor binding + 0.9062 90.62%
Aromatase binding + 0.6314 63.14%
PPAR gamma + 0.9245 92.45%
Honey bee toxicity - 0.8383 83.83%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9946 99.46%

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 99.52% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 98.99% 91.49%
CHEMBL2581 P07339 Cathepsin D 97.22% 98.95%
CHEMBL1929 P47989 Xanthine dehydrogenase 95.62% 96.12%
CHEMBL3401 O75469 Pregnane X receptor 94.93% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.52% 89.00%
CHEMBL3194 P02766 Transthyretin 91.53% 90.71%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.32% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.64% 95.56%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 88.35% 89.34%
CHEMBL3038469 P24941 CDK2/Cyclin A 86.39% 91.38%
CHEMBL4208 P20618 Proteasome component C5 85.83% 90.00%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 85.03% 95.64%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 84.46% 98.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.77% 99.17%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 83.60% 99.15%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.34% 90.71%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.11% 94.00%

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.
Artocarpus heterophyllus
Morus alba

Cross-Links

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PubChem 15231527
NPASS NPC71429
LOTUS LTS0086833
wikiData Q105137992