Cowanin

Details

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Internal ID f1ce3d00-dde9-4b95-a06f-90804cdfe6fe
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Xanthones > 8-prenylated xanthones
IUPAC Name 1-[(2E)-3,7-dimethylocta-2,6-dienyl]-3,6,8-trihydroxy-2-methoxy-7-(3-methylbut-2-enyl)xanthen-9-one
SMILES (Canonical) CC(=CCCC(=CCC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)OC)C)C
SMILES (Isomeric) CC(=CCC/C(=C/CC1=C(C(=CC2=C1C(=O)C3=C(O2)C=C(C(=C3O)CC=C(C)C)O)O)OC)/C)C
InChI InChI=1S/C29H34O6/c1-16(2)8-7-9-18(5)11-13-20-25-23(15-22(31)29(20)34-6)35-24-14-21(30)19(12-10-17(3)4)27(32)26(24)28(25)33/h8,10-11,14-15,30-32H,7,9,12-13H2,1-6H3/b18-11+
InChI Key GVDDDYKLKUMEGV-WOJGMQOQSA-N
Popularity 7 references in papers

Physical and Chemical Properties

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Molecular Formula C29H34O6
Molecular Weight 478.60 g/mol
Exact Mass 478.23553880 g/mol
Topological Polar Surface Area (TPSA) 96.20 Ų
XlogP 8.10
Atomic LogP (AlogP) 6.82
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 8

Synonyms

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CHEMBL458845
BDBM50370158
NSC752810
NSC-752810

2D Structure

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2D Structure of Cowanin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9549 95.49%
Caco-2 - 0.6293 62.93%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability + 0.6000 60.00%
Subcellular localzation Mitochondria 0.6725 67.25%
OATP2B1 inhibitior - 0.5716 57.16%
OATP1B1 inhibitior + 0.9220 92.20%
OATP1B3 inhibitior + 0.8952 89.52%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.7064 70.64%
BSEP inhibitior + 0.8639 86.39%
P-glycoprotein inhibitior + 0.8149 81.49%
P-glycoprotein substrate - 0.8021 80.21%
CYP3A4 substrate + 0.5769 57.69%
CYP2C9 substrate - 0.5929 59.29%
CYP2D6 substrate - 0.8145 81.45%
CYP3A4 inhibition - 0.5831 58.31%
CYP2C9 inhibition + 0.6416 64.16%
CYP2C19 inhibition + 0.7742 77.42%
CYP2D6 inhibition + 0.5415 54.15%
CYP1A2 inhibition + 0.8912 89.12%
CYP2C8 inhibition + 0.4449 44.49%
CYP inhibitory promiscuity + 0.7164 71.64%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7801 78.01%
Eye corrosion - 0.9895 98.95%
Eye irritation - 0.8275 82.75%
Skin irritation - 0.7616 76.16%
Skin corrosion - 0.9375 93.75%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8508 85.08%
Micronuclear - 0.7800 78.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8069 80.69%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8778 87.78%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity - 0.9125 91.25%
Acute Oral Toxicity (c) III 0.4866 48.66%
Estrogen receptor binding + 0.8801 88.01%
Androgen receptor binding + 0.6763 67.63%
Thyroid receptor binding + 0.5826 58.26%
Glucocorticoid receptor binding + 0.8434 84.34%
Aromatase binding + 0.7172 71.72%
PPAR gamma + 0.8138 81.38%
Honey bee toxicity - 0.7298 72.98%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.9972 99.72%

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 99.47% 91.11%
CHEMBL2581 P07339 Cathepsin D 94.36% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 94.22% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.58% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.83% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 89.21% 89.34%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.34% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.11% 86.33%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 87.39% 92.08%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.34% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.30% 85.14%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 84.38% 98.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.57% 96.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.64% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.55% 96.00%

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.
Garcinia cowa
Garcinia dulcis
Garcinia fusca
Garcinia oliveri

Cross-Links

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PubChem 11754819
NPASS NPC40491
LOTUS LTS0098372
wikiData Q104399143