Triumbelletin

Details

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Internal ID 3a75b005-4f9f-41b7-b17a-93a771bfb566
Taxonomy Phenylpropanoids and polyketides > Coumarins and derivatives > Hydroxycoumarins > 7-hydroxycoumarins
IUPAC Name 7-hydroxy-8-(7-hydroxy-2-oxochromen-8-yl)-3-(2-oxochromen-7-yl)oxychromen-2-one
SMILES (Canonical) C1=CC(=CC2=C1C=CC(=O)O2)OC3=CC4=C(C(=C(C=C4)O)C5=C(C=CC6=C5OC(=O)C=C6)O)OC3=O
SMILES (Isomeric) C1=CC(=CC2=C1C=CC(=O)O2)OC3=CC4=C(C(=C(C=C4)O)C5=C(C=CC6=C5OC(=O)C=C6)O)OC3=O
InChI InChI=1S/C27H14O9/c28-17-7-2-14-5-10-22(31)35-25(14)23(17)24-18(29)8-3-15-11-20(27(32)36-26(15)24)33-16-6-1-13-4-9-21(30)34-19(13)12-16/h1-12,28-29H
InChI Key GDHDMCIEKMVPIP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C27H14O9
Molecular Weight 482.40 g/mol
Exact Mass 482.06378202 g/mol
Topological Polar Surface Area (TPSA) 129.00 Ų
XlogP 4.50
Atomic LogP (AlogP) 4.88
H-Bond Acceptor 9
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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131559-54-1
7-hydroxy-8-(7-hydroxy-2-oxochromen-8-yl)-3-(2-oxochromen-7-yl)oxychromen-2-one
AKOS040760088
HY-133181
CS-0113143

2D Structure

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2D Structure of Triumbelletin

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9178 91.78%
Caco-2 - 0.9012 90.12%
Blood Brain Barrier - 0.9250 92.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.8207 82.07%
OATP2B1 inhibitior + 0.5676 56.76%
OATP1B1 inhibitior + 0.8410 84.10%
OATP1B3 inhibitior + 0.9171 91.71%
MATE1 inhibitior - 0.8000 80.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior + 0.6052 60.52%
P-glycoprotein inhibitior + 0.7077 70.77%
P-glycoprotein substrate - 0.9080 90.80%
CYP3A4 substrate - 0.5303 53.03%
CYP2C9 substrate - 0.8103 81.03%
CYP2D6 substrate - 0.8391 83.91%
CYP3A4 inhibition - 0.9095 90.95%
CYP2C9 inhibition + 0.8595 85.95%
CYP2C19 inhibition - 0.6028 60.28%
CYP2D6 inhibition - 0.9510 95.10%
CYP1A2 inhibition - 0.7968 79.68%
CYP2C8 inhibition + 0.5883 58.83%
CYP inhibitory promiscuity - 0.7466 74.66%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6253 62.53%
Eye corrosion - 0.9900 99.00%
Eye irritation - 0.6564 65.64%
Skin irritation - 0.5873 58.73%
Skin corrosion - 0.9710 97.10%
Ames mutagenesis + 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4884 48.84%
Micronuclear + 0.9200 92.00%
Hepatotoxicity - 0.5458 54.58%
skin sensitisation - 0.9129 91.29%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.5299 52.99%
Acute Oral Toxicity (c) II 0.5064 50.64%
Estrogen receptor binding + 0.8798 87.98%
Androgen receptor binding + 0.9145 91.45%
Thyroid receptor binding - 0.5073 50.73%
Glucocorticoid receptor binding + 0.7454 74.54%
Aromatase binding + 0.5430 54.30%
PPAR gamma + 0.8319 83.19%
Honey bee toxicity - 0.8563 85.63%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity - 0.5199 51.99%
Fish aquatic toxicity + 0.9633 96.33%

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 98.46% 91.11%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 97.63% 99.15%
CHEMBL1951 P21397 Monoamine oxidase A 95.81% 91.49%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 94.86% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.02% 95.56%
CHEMBL4208 P20618 Proteasome component C5 90.23% 90.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.68% 99.23%
CHEMBL3194 P02766 Transthyretin 89.10% 90.71%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.24% 86.92%
CHEMBL2085 P14174 Macrophage migration inhibitory factor 87.98% 80.78%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.23% 99.17%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 83.15% 83.57%
CHEMBL3401 O75469 Pregnane X receptor 82.83% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.64% 90.71%
CHEMBL2581 P07339 Cathepsin D 82.40% 98.95%
CHEMBL2535 P11166 Glucose transporter 81.95% 98.75%
CHEMBL5339 Q5NUL3 G-protein coupled receptor 120 81.20% 95.78%
CHEMBL4531 P17931 Galectin-3 81.17% 96.90%

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.
Daphne mezereum

Cross-Links

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PubChem 14213530
LOTUS LTS0049639
wikiData Q105006712