5-Hydroxyphomopsinone A

Details

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Internal ID 52222572-e8af-4594-b48c-f65225de8fa6
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name (5R,7S)-5-hydroxy-4-methoxy-7-propyl-7,8-dihydro-5H-pyrano[4,3-b]pyran-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C12H16O5/c1-3-4-7-5-9-11(12(14)16-7)8(15-2)6-10(13)17-9/h6-7,12,14H,3-5H2,1-2H3/t7-,12+/m0/s1
InChI Key VTAGIXKLJWOHCH-JVXZTZIISA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C12H16O5
Molecular Weight 240.25 g/mol
Exact Mass 240.09977361 g/mol
Topological Polar Surface Area (TPSA) 65.00 Ų
XlogP 0.50
Atomic LogP (AlogP) 1.38
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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CHEMBL3943190

2D Structure

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2D Structure of 5-Hydroxyphomopsinone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9453 94.53%
Caco-2 + 0.7257 72.57%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7026 70.26%
OATP2B1 inhibitior - 0.8510 85.10%
OATP1B1 inhibitior + 0.9168 91.68%
OATP1B3 inhibitior + 0.9150 91.50%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.8453 84.53%
P-glycoprotein inhibitior - 0.8824 88.24%
P-glycoprotein substrate - 0.7778 77.78%
CYP3A4 substrate - 0.5309 53.09%
CYP2C9 substrate - 0.5890 58.90%
CYP2D6 substrate - 0.8538 85.38%
CYP3A4 inhibition - 0.8224 82.24%
CYP2C9 inhibition - 0.6191 61.91%
CYP2C19 inhibition - 0.5481 54.81%
CYP2D6 inhibition - 0.7893 78.93%
CYP1A2 inhibition + 0.5658 56.58%
CYP2C8 inhibition - 0.8760 87.60%
CYP inhibitory promiscuity - 0.5549 55.49%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6508 65.08%
Eye corrosion - 0.9808 98.08%
Eye irritation - 0.8346 83.46%
Skin irritation - 0.8037 80.37%
Skin corrosion - 0.9472 94.72%
Ames mutagenesis - 0.5954 59.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5079 50.79%
Micronuclear - 0.6900 69.00%
Hepatotoxicity - 0.6073 60.73%
skin sensitisation - 0.8368 83.68%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.6455 64.55%
Acute Oral Toxicity (c) III 0.4759 47.59%
Estrogen receptor binding + 0.5914 59.14%
Androgen receptor binding - 0.5267 52.67%
Thyroid receptor binding - 0.5775 57.75%
Glucocorticoid receptor binding - 0.5083 50.83%
Aromatase binding - 0.6641 66.41%
PPAR gamma + 0.6326 63.26%
Honey bee toxicity - 0.9270 92.70%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5749 57.49%
Fish aquatic toxicity + 0.8967 89.67%

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 97.10% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 95.59% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.82% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 91.76% 94.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.57% 86.33%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.31% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.21% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.01% 97.09%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 85.53% 92.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.13% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.93% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.83% 89.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.51% 96.95%
CHEMBL3401 O75469 Pregnane X receptor 83.70% 94.73%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 82.77% 90.71%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.83% 85.14%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.57% 97.14%
CHEMBL241 Q14432 Phosphodiesterase 3A 81.55% 92.94%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 134146121
LOTUS LTS0255807
wikiData Q105292631