Torrubiellone C

Details

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Internal ID 039094f5-c90f-42c2-b8b3-308d54c274f9
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Phenylpyridines
IUPAC Name 4-hydroxy-3-[(2E,4E,6E)-8-(hydroxymethyl)deca-2,4,6-trienoyl]-5-(4-hydroxyphenyl)-1H-pyridin-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H23NO5/c1-2-15(14-24)7-5-3-4-6-8-19(26)20-21(27)18(13-23-22(20)28)16-9-11-17(25)12-10-16/h3-13,15,24-25H,2,14H2,1H3,(H2,23,27,28)/b4-3+,7-5+,8-6+
InChI Key BKSPTJGGAGGDSV-OKWWDJPNSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C22H23NO5
Molecular Weight 381.40 g/mol
Exact Mass 381.15762283 g/mol
Topological Polar Surface Area (TPSA) 107.00 Ų
XlogP 2.80
Atomic LogP (AlogP) 3.32
H-Bond Acceptor 5
H-Bond Donor 4
Rotatable Bonds 8

Synonyms

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CHEMBL4072771
CHEBI:70288
Q27138628

2D Structure

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2D Structure of Torrubiellone C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9848 98.48%
Caco-2 - 0.7016 70.16%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7245 72.45%
OATP2B1 inhibitior - 0.5782 57.82%
OATP1B1 inhibitior + 0.7531 75.31%
OATP1B3 inhibitior + 0.9344 93.44%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8710 87.10%
P-glycoprotein inhibitior - 0.6525 65.25%
P-glycoprotein substrate - 0.6680 66.80%
CYP3A4 substrate + 0.5693 56.93%
CYP2C9 substrate + 0.5965 59.65%
CYP2D6 substrate - 0.8786 87.86%
CYP3A4 inhibition - 0.6725 67.25%
CYP2C9 inhibition - 0.8012 80.12%
CYP2C19 inhibition - 0.6038 60.38%
CYP2D6 inhibition - 0.8981 89.81%
CYP1A2 inhibition + 0.5627 56.27%
CYP2C8 inhibition + 0.5443 54.43%
CYP inhibitory promiscuity - 0.6478 64.78%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.7023 70.23%
Eye corrosion - 0.9937 99.37%
Eye irritation - 0.9051 90.51%
Skin irritation - 0.8292 82.92%
Skin corrosion - 0.9499 94.99%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4365 43.65%
Micronuclear + 0.7400 74.00%
Hepatotoxicity + 0.5005 50.05%
skin sensitisation - 0.8405 84.05%
Respiratory toxicity + 0.6667 66.67%
Reproductive toxicity + 0.6889 68.89%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity - 0.8678 86.78%
Acute Oral Toxicity (c) III 0.7276 72.76%
Estrogen receptor binding + 0.7724 77.24%
Androgen receptor binding + 0.8465 84.65%
Thyroid receptor binding + 0.5537 55.37%
Glucocorticoid receptor binding + 0.5783 57.83%
Aromatase binding + 0.6952 69.52%
PPAR gamma + 0.8513 85.13%
Honey bee toxicity - 0.8781 87.81%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.8359 83.59%

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 96.55% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.47% 96.09%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 91.22% 83.10%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 91.13% 91.71%
CHEMBL2345 P51812 Ribosomal protein S6 kinase alpha 3 90.12% 95.64%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.24% 91.11%
CHEMBL242 Q92731 Estrogen receptor beta 88.45% 98.35%
CHEMBL1806 P11388 DNA topoisomerase II alpha 88.16% 89.00%
CHEMBL268 P43235 Cathepsin K 87.13% 96.85%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.59% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.58% 95.56%
CHEMBL3922 P50579 Methionine aminopeptidase 2 85.26% 97.28%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.98% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.96% 99.17%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 81.83% 86.92%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.76% 90.71%
CHEMBL2996 Q05655 Protein kinase C delta 80.65% 97.79%

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 54729462
LOTUS LTS0209153
wikiData Q27138628