Citrinolactone C

Details

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Internal ID bde89b88-2068-4efe-87b6-6abcb637a6f4
Taxonomy Phenylpropanoids and polyketides > Isocoumarins and derivatives
IUPAC Name [(1S)-6-hydroxy-8-methyl-5-oxo-2,3-dihydro-1H-cyclopenta[c]isochromen-1-yl] acetate
SMILES (Canonical) CC1=CC2=C(C(=C1)O)C(=O)OC3=C2C(CC3)OC(=O)C
SMILES (Isomeric) CC1=CC2=C(C(=C1)O)C(=O)OC3=C2[C@H](CC3)OC(=O)C
InChI InChI=1S/C15H14O5/c1-7-5-9-13(10(17)6-7)15(18)20-12-4-3-11(14(9)12)19-8(2)16/h5-6,11,17H,3-4H2,1-2H3/t11-/m0/s1
InChI Key FJRYQTQEJSGKMI-NSHDSACASA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C15H14O5
Molecular Weight 274.27 g/mol
Exact Mass 274.08412354 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.36
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Citrinolactone C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9652 96.52%
Caco-2 + 0.7156 71.56%
Blood Brain Barrier - 0.7000 70.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.7783 77.83%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9318 93.18%
OATP1B3 inhibitior + 0.9514 95.14%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.7798 77.98%
P-glycoprotein inhibitior - 0.8038 80.38%
P-glycoprotein substrate - 0.8552 85.52%
CYP3A4 substrate + 0.5704 57.04%
CYP2C9 substrate + 0.8452 84.52%
CYP2D6 substrate - 0.8766 87.66%
CYP3A4 inhibition - 0.8358 83.58%
CYP2C9 inhibition + 0.5368 53.68%
CYP2C19 inhibition - 0.6771 67.71%
CYP2D6 inhibition - 0.9020 90.20%
CYP1A2 inhibition + 0.7665 76.65%
CYP2C8 inhibition - 0.6437 64.37%
CYP inhibitory promiscuity - 0.8282 82.82%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6667 66.67%
Eye corrosion - 0.9831 98.31%
Eye irritation - 0.5915 59.15%
Skin irritation - 0.7820 78.20%
Skin corrosion - 0.9429 94.29%
Ames mutagenesis - 0.5264 52.64%
Human Ether-a-go-go-Related Gene inhibition - 0.6530 65.30%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.5981 59.81%
skin sensitisation - 0.9006 90.06%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.8122 81.22%
Acute Oral Toxicity (c) III 0.4340 43.40%
Estrogen receptor binding + 0.7512 75.12%
Androgen receptor binding + 0.7050 70.50%
Thyroid receptor binding - 0.6515 65.15%
Glucocorticoid receptor binding + 0.6174 61.74%
Aromatase binding - 0.6871 68.71%
PPAR gamma + 0.8068 80.68%
Honey bee toxicity - 0.8658 86.58%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6400 64.00%
Fish aquatic toxicity + 0.8950 89.50%

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 99.57% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 94.51% 89.00%
CHEMBL2581 P07339 Cathepsin D 93.98% 98.95%
CHEMBL1951 P21397 Monoamine oxidase A 93.14% 91.49%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.80% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.62% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 88.78% 91.19%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.61% 94.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 87.58% 94.80%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.48% 85.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.79% 99.23%
CHEMBL241 Q14432 Phosphodiesterase 3A 84.53% 92.94%
CHEMBL3401 O75469 Pregnane X receptor 82.55% 94.73%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.00% 93.04%
CHEMBL2094127 P06493 Cyclin-dependent kinase 1/cyclin B 81.81% 96.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.39% 100.00%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.26% 93.65%

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 102595351
LOTUS LTS0145431
wikiData Q77374604