Hypocrellone A

Details

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Internal ID e8b90b4b-08f4-401e-a575-461918d8a87e
Taxonomy Organoheterocyclic compounds > Azaphilones
IUPAC Name 5-chloro-3-[(3R,4R,5S)-3,4-dihydroxy-3,5-dimethylhept-1-enyl]-7,8-dihydroxy-7-methyl-8H-isochromen-6-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H25ClO6/c1-5-10(2)15(21)18(3,24)7-6-11-8-12-13(9-26-11)16(22)19(4,25)17(23)14(12)20/h6-10,15-16,21-22,24-25H,5H2,1-4H3/t10-,15+,16?,18+,19?/m0/s1
InChI Key BRELKNNWUMEGDN-GHCXSWNOSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H25ClO6
Molecular Weight 384.80 g/mol
Exact Mass 384.1339662 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 0.70
Atomic LogP (AlogP) 1.69
H-Bond Acceptor 6
H-Bond Donor 4
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hypocrellone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9783 97.83%
Caco-2 - 0.7070 70.70%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6571 65.71%
Subcellular localzation Mitochondria 0.6020 60.20%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7996 79.96%
OATP1B3 inhibitior + 0.9268 92.68%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.6217 62.17%
P-glycoprotein inhibitior - 0.8173 81.73%
P-glycoprotein substrate - 0.6494 64.94%
CYP3A4 substrate + 0.6475 64.75%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8585 85.85%
CYP3A4 inhibition - 0.7012 70.12%
CYP2C9 inhibition - 0.6517 65.17%
CYP2C19 inhibition - 0.6456 64.56%
CYP2D6 inhibition - 0.8462 84.62%
CYP1A2 inhibition - 0.7521 75.21%
CYP2C8 inhibition - 0.6576 65.76%
CYP inhibitory promiscuity - 0.5201 52.01%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9000 90.00%
Carcinogenicity (trinary) Non-required 0.4369 43.69%
Eye corrosion - 0.9856 98.56%
Eye irritation - 0.9686 96.86%
Skin irritation - 0.6083 60.83%
Skin corrosion - 0.9090 90.90%
Ames mutagenesis - 0.5400 54.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3843 38.43%
Micronuclear - 0.6600 66.00%
Hepatotoxicity + 0.6213 62.13%
skin sensitisation - 0.7516 75.16%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.6016 60.16%
Acute Oral Toxicity (c) III 0.5061 50.61%
Estrogen receptor binding + 0.8123 81.23%
Androgen receptor binding + 0.6876 68.76%
Thyroid receptor binding + 0.7167 71.67%
Glucocorticoid receptor binding + 0.6680 66.80%
Aromatase binding + 0.7407 74.07%
PPAR gamma + 0.6675 66.75%
Honey bee toxicity - 0.7893 78.93%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5900 59.00%
Fish aquatic toxicity + 0.9810 98.10%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.68% 97.25%
CHEMBL2581 P07339 Cathepsin D 98.68% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 98.40% 89.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.88% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 94.42% 94.73%
CHEMBL218 P21554 Cannabinoid CB1 receptor 92.08% 96.61%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.23% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.82% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 90.62% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.15% 96.09%
CHEMBL226 P30542 Adenosine A1 receptor 89.02% 95.93%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.19% 85.14%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 85.70% 92.88%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 85.43% 85.94%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.26% 97.09%
CHEMBL3922 P50579 Methionine aminopeptidase 2 82.56% 97.28%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.42% 86.92%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.51% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.16% 95.71%

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.
There are no matching plants.

Cross-Links

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PubChem 139588582
LOTUS LTS0245809
wikiData Q104944750