5-Hydroxy-2-nonadec-14-enylchromen-4-one

Details

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Internal ID 6fa26af7-1170-4505-bb59-2ef797edad17
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 5-hydroxy-2-nonadec-14-enylchromen-4-one
SMILES (Canonical) CCCCC=CCCCCCCCCCCCCCC1=CC(=O)C2=C(C=CC=C2O1)O
SMILES (Isomeric) CCCCC=CCCCCCCCCCCCCCC1=CC(=O)C2=C(C=CC=C2O1)O
InChI InChI=1S/C28H42O3/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-20-24-23-26(30)28-25(29)21-19-22-27(28)31-24/h5-6,19,21-23,29H,2-4,7-18,20H2,1H3
InChI Key HXSMRENEMIEUND-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H42O3
Molecular Weight 426.60 g/mol
Exact Mass 426.31339520 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 10.60
Atomic LogP (AlogP) 8.47
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 17

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Hydroxy-2-nonadec-14-enylchromen-4-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.6786 67.86%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Plasma membrane 0.8966 89.66%
OATP2B1 inhibitior - 0.8574 85.74%
OATP1B1 inhibitior + 0.8766 87.66%
OATP1B3 inhibitior + 0.9753 97.53%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.5944 59.44%
P-glycoprotein inhibitior + 0.6520 65.20%
P-glycoprotein substrate - 0.7397 73.97%
CYP3A4 substrate + 0.5208 52.08%
CYP2C9 substrate - 0.5826 58.26%
CYP2D6 substrate - 0.8297 82.97%
CYP3A4 inhibition + 0.5262 52.62%
CYP2C9 inhibition - 0.8709 87.09%
CYP2C19 inhibition + 0.6356 63.56%
CYP2D6 inhibition - 0.9173 91.73%
CYP1A2 inhibition + 0.8203 82.03%
CYP2C8 inhibition + 0.4578 45.78%
CYP inhibitory promiscuity - 0.5269 52.69%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6054 60.54%
Eye corrosion - 0.9712 97.12%
Eye irritation - 0.5792 57.92%
Skin irritation - 0.6534 65.34%
Skin corrosion - 0.9265 92.65%
Ames mutagenesis - 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6479 64.79%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5448 54.48%
skin sensitisation - 0.7489 74.89%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6752 67.52%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.6304 63.04%
Acute Oral Toxicity (c) III 0.6564 65.64%
Estrogen receptor binding + 0.6430 64.30%
Androgen receptor binding + 0.7293 72.93%
Thyroid receptor binding - 0.5547 55.47%
Glucocorticoid receptor binding - 0.5062 50.62%
Aromatase binding - 0.5278 52.78%
PPAR gamma + 0.6378 63.78%
Honey bee toxicity - 0.9741 97.41%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.6024 60.24%
Fish aquatic toxicity + 0.9892 98.92%

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
CHEMBL2581 P07339 Cathepsin D 98.88% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.74% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.36% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 95.97% 94.73%
CHEMBL3192 Q9BY41 Histone deacetylase 8 93.85% 93.99%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.69% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.65% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 92.81% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.68% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.72% 94.45%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.77% 89.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.39% 96.95%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.92% 90.71%
CHEMBL1781 P11387 DNA topoisomerase I 82.33% 97.00%
CHEMBL1907 P15144 Aminopeptidase N 81.18% 93.31%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.13% 99.23%
CHEMBL3891 P07384 Calpain 1 80.91% 93.04%
CHEMBL1937 Q92769 Histone deacetylase 2 80.58% 94.75%

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.
Peperomia vulcanica

Cross-Links

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PubChem 6325795
NPASS NPC15180
LOTUS LTS0061571
wikiData Q105035136