Phaeochromycin D

Details

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Internal ID 0860321e-054a-46aa-ada9-b5ebacfa46fb
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Chromones
IUPAC Name 5-(4-hydroxy-2-oxopentyl)-2-propylchromen-4-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H20O4/c1-3-5-14-10-15(20)17-12(6-4-7-16(17)21-14)9-13(19)8-11(2)18/h4,6-7,10-11,18H,3,5,8-9H2,1-2H3
InChI Key RNGDSOLGWNOHCR-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H20O4
Molecular Weight 288.34 g/mol
Exact Mass 288.13615911 g/mol
Topological Polar Surface Area (TPSA) 63.60 Ų
XlogP 2.00
Atomic LogP (AlogP) 2.63
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Phaeochromycin D

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9615 96.15%
Caco-2 + 0.7000 70.00%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.6113 61.13%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9267 92.67%
OATP1B3 inhibitior + 0.9674 96.74%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5559 55.59%
P-glycoprotein inhibitior - 0.8595 85.95%
P-glycoprotein substrate - 0.6181 61.81%
CYP3A4 substrate - 0.5064 50.64%
CYP2C9 substrate - 0.5928 59.28%
CYP2D6 substrate - 0.8068 80.68%
CYP3A4 inhibition + 0.5805 58.05%
CYP2C9 inhibition - 0.7769 77.69%
CYP2C19 inhibition - 0.7458 74.58%
CYP2D6 inhibition - 0.9044 90.44%
CYP1A2 inhibition - 0.5081 50.81%
CYP2C8 inhibition - 0.8161 81.61%
CYP inhibitory promiscuity - 0.8172 81.72%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6277 62.77%
Eye corrosion - 0.9869 98.69%
Eye irritation - 0.8512 85.12%
Skin irritation - 0.7300 73.00%
Skin corrosion - 0.8831 88.31%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3724 37.24%
Micronuclear - 0.6200 62.00%
Hepatotoxicity + 0.5375 53.75%
skin sensitisation - 0.8875 88.75%
Respiratory toxicity + 0.6889 68.89%
Reproductive toxicity + 0.8556 85.56%
Mitochondrial toxicity + 0.8000 80.00%
Nephrotoxicity - 0.5643 56.43%
Acute Oral Toxicity (c) III 0.6574 65.74%
Estrogen receptor binding - 0.6574 65.74%
Androgen receptor binding + 0.6392 63.92%
Thyroid receptor binding - 0.7658 76.58%
Glucocorticoid receptor binding + 0.6971 69.71%
Aromatase binding - 0.5470 54.70%
PPAR gamma + 0.7738 77.38%
Honey bee toxicity - 0.9363 93.63%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7300 73.00%
Fish aquatic toxicity + 0.8700 87.00%

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 98.83% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.76% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 93.93% 94.73%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.28% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 91.03% 89.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 90.35% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.28% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.99% 96.09%
CHEMBL2535 P11166 Glucose transporter 86.94% 98.75%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.76% 96.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.78% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.51% 94.45%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.90% 95.50%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 81.47% 100.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.36% 99.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 80.36% 92.62%

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 11709038
LOTUS LTS0020908
wikiData Q77519466