Phialophoriol

Details

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Internal ID da186d6b-fb83-438d-bfb6-7b45e51a3475
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name (1S,3S)-3,6-dihydroxy-8-methoxy-1-methyl-2,3-dihydro-1H-cyclopenta[c]isochromen-5-one
SMILES (Canonical) CC1CC(C2=C1C3=C(C(=CC(=C3)OC)O)C(=O)O2)O
SMILES (Isomeric) C[C@H]1C[C@@H](C2=C1C3=C(C(=CC(=C3)OC)O)C(=O)O2)O
InChI InChI=1S/C14H14O5/c1-6-3-10(16)13-11(6)8-4-7(18-2)5-9(15)12(8)14(17)19-13/h4-6,10,15-16H,3H2,1-2H3/t6-,10-/m0/s1
InChI Key LYMFBENHIQPDBU-WKEGUHRASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C14H14O5
Molecular Weight 262.26 g/mol
Exact Mass 262.08412354 g/mol
Topological Polar Surface Area (TPSA) 76.00 Ų
XlogP 1.50
Atomic LogP (AlogP) 2.05
H-Bond Acceptor 5
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Phialophoriol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9722 97.22%
Caco-2 + 0.7096 70.96%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Mitochondria 0.6075 60.75%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9235 92.35%
OATP1B3 inhibitior + 0.8539 85.39%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.5579 55.79%
P-glycoprotein inhibitior - 0.8943 89.43%
P-glycoprotein substrate - 0.6965 69.65%
CYP3A4 substrate + 0.5385 53.85%
CYP2C9 substrate + 0.6825 68.25%
CYP2D6 substrate - 0.8331 83.31%
CYP3A4 inhibition - 0.8035 80.35%
CYP2C9 inhibition - 0.8666 86.66%
CYP2C19 inhibition - 0.6820 68.20%
CYP2D6 inhibition - 0.6099 60.99%
CYP1A2 inhibition + 0.7631 76.31%
CYP2C8 inhibition - 0.7410 74.10%
CYP inhibitory promiscuity - 0.8093 80.93%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5546 55.46%
Eye corrosion - 0.9810 98.10%
Eye irritation - 0.6667 66.67%
Skin irritation - 0.7550 75.50%
Skin corrosion - 0.9658 96.58%
Ames mutagenesis + 0.6263 62.63%
Human Ether-a-go-go-Related Gene inhibition - 0.8132 81.32%
Micronuclear + 0.7700 77.00%
Hepatotoxicity + 0.5323 53.23%
skin sensitisation - 0.8692 86.92%
Respiratory toxicity + 0.6333 63.33%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7000 70.00%
Nephrotoxicity - 0.8316 83.16%
Acute Oral Toxicity (c) III 0.5223 52.23%
Estrogen receptor binding + 0.6238 62.38%
Androgen receptor binding + 0.7717 77.17%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7458 74.58%
Aromatase binding - 0.6620 66.20%
PPAR gamma + 0.7417 74.17%
Honey bee toxicity - 0.7359 73.59%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.5000 50.00%
Fish aquatic toxicity + 0.8317 83.17%

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 99.30% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 96.49% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.57% 95.56%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 92.50% 94.00%
CHEMBL241 Q14432 Phosphodiesterase 3A 90.89% 92.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.65% 97.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.27% 89.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 89.21% 94.45%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 87.86% 99.15%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.03% 85.14%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.90% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.38% 98.95%
CHEMBL2535 P11166 Glucose transporter 82.71% 98.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.31% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.92% 95.89%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.26% 99.23%
CHEMBL4208 P20618 Proteasome component C5 81.10% 90.00%

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.
Salvia kronenburgii

Cross-Links

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PubChem 72193405
LOTUS LTS0107118
wikiData Q105372421