Pongamol

Details

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Internal ID 72548ee4-3ea1-40a7-9aec-e4ba88e88dea
Taxonomy Phenylpropanoids and polyketides > Linear 1,3-diarylpropanoids > Chalcones and dihydrochalcones > Retro-dihydrochalcones
IUPAC Name 1-(4-methoxy-1-benzofuran-5-yl)-3-phenylpropane-1,3-dione
SMILES (Canonical) COC1=C(C=CC2=C1C=CO2)C(=O)CC(=O)C3=CC=CC=C3
SMILES (Isomeric) COC1=C(C=CC2=C1C=CO2)C(=O)CC(=O)C3=CC=CC=C3
InChI InChI=1S/C18H14O4/c1-21-18-13(7-8-17-14(18)9-10-22-17)16(20)11-15(19)12-5-3-2-4-6-12/h2-10H,11H2,1H3
InChI Key XTLSKKJNOIMMBK-UHFFFAOYSA-N
Popularity 20 references in papers

Physical and Chemical Properties

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Molecular Formula C18H14O4
Molecular Weight 294.30 g/mol
Exact Mass 294.08920892 g/mol
Topological Polar Surface Area (TPSA) 56.50 Ų
XlogP 3.50
Atomic LogP (AlogP) 3.90
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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484-33-3
Lanceolatin C
1,3-Propanedione, 1-(4-methoxy-5-benzofuranyl)-3-phenyl-
8Y19QCY6I4
1-(4-methoxy-1-benzofuran-5-yl)-3-phenylpropane-1,3-dione
1-(4-Methoxy-benzofuran-5-yl)-3-phenyl-propane-1,3-dione
1-(4-methoxybenzofuran-5-yl)-3-phenylpropane-1,3-dione
BIDD:ER0486
starbld0009680
PONGAMOL [INCI]
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Pongamol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9965 99.65%
Caco-2 + 0.8768 87.68%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7429 74.29%
OATP2B1 inhibitior - 0.8633 86.33%
OATP1B1 inhibitior + 0.9301 93.01%
OATP1B3 inhibitior + 0.9924 99.24%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5610 56.10%
P-glycoprotein inhibitior - 0.5183 51.83%
P-glycoprotein substrate - 0.8570 85.70%
CYP3A4 substrate - 0.5691 56.91%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7158 71.58%
CYP3A4 inhibition - 0.7240 72.40%
CYP2C9 inhibition + 0.8799 87.99%
CYP2C19 inhibition + 0.8629 86.29%
CYP2D6 inhibition - 0.8727 87.27%
CYP1A2 inhibition + 0.9578 95.78%
CYP2C8 inhibition + 0.6015 60.15%
CYP inhibitory promiscuity + 0.8609 86.09%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9043 90.43%
Carcinogenicity (trinary) Non-required 0.4032 40.32%
Eye corrosion - 0.9680 96.80%
Eye irritation - 0.8049 80.49%
Skin irritation - 0.7958 79.58%
Skin corrosion - 0.9699 96.99%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6866 68.66%
Micronuclear + 0.7077 70.77%
Hepatotoxicity - 0.5285 52.85%
skin sensitisation - 0.8463 84.63%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.7830 78.30%
Acute Oral Toxicity (c) III 0.4868 48.68%
Estrogen receptor binding + 0.9370 93.70%
Androgen receptor binding + 0.6863 68.63%
Thyroid receptor binding - 0.5899 58.99%
Glucocorticoid receptor binding + 0.7414 74.14%
Aromatase binding + 0.7261 72.61%
PPAR gamma + 0.5782 57.82%
Honey bee toxicity - 0.8841 88.41%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.9489 94.89%

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 91.83% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 91.06% 90.17%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.05% 99.17%
CHEMBL2535 P11166 Glucose transporter 90.79% 98.75%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.53% 95.56%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.67% 99.23%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 86.53% 81.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.38% 86.33%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 85.20% 87.67%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.95% 85.14%
CHEMBL2581 P07339 Cathepsin D 82.50% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.17% 96.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.47% 96.00%
CHEMBL5028 O14672 ADAM10 81.39% 97.50%
CHEMBL3401 O75469 Pregnane X receptor 81.00% 94.73%

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.
Dahlstedtia pinnata
Derris ovalifolia
Millettia erythrocalyx
Millettia peguensis
Millettia sanagana
Pongamia pinnata
Tephrosia falciformis
Tephrosia purpurea

Cross-Links

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PubChem 689051
LOTUS LTS0015247
wikiData Q27271185