Ent-Ircinialactam C

Details

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Internal ID a57e3c77-0635-4a94-93d2-cd84f1620fda
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids
IUPAC Name (3R,7E,11E)-14-[1-(carboxymethyl)-5-oxo-2H-pyrrol-4-yl]-3,7,11-trimethyltetradeca-7,11-dienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C23H35NO5/c1-17(9-5-11-19(3)15-21(25)26)7-4-8-18(2)10-6-12-20-13-14-24(23(20)29)16-22(27)28/h7,10,13,19H,4-6,8-9,11-12,14-16H2,1-3H3,(H,25,26)(H,27,28)/b17-7+,18-10+/t19-/m1/s1
InChI Key FYWCTUYAFXXJQJ-CVUGZRRRSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C23H35NO5
Molecular Weight 405.50 g/mol
Exact Mass 405.25152322 g/mol
Topological Polar Surface Area (TPSA) 94.90 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.57
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 14

Synonyms

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CHEMBL1092618
BDBM50316017

2D Structure

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2D Structure of Ent-Ircinialactam C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6181 61.81%
Caco-2 - 0.5988 59.88%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6339 63.39%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9078 90.78%
OATP1B3 inhibitior + 0.9288 92.88%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.8446 84.46%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.6433 64.33%
CYP3A4 substrate + 0.5803 58.03%
CYP2C9 substrate + 1.0000 100.00%
CYP2D6 substrate - 0.9182 91.82%
CYP3A4 inhibition - 0.9177 91.77%
CYP2C9 inhibition - 0.8975 89.75%
CYP2C19 inhibition - 0.8007 80.07%
CYP2D6 inhibition - 0.9156 91.56%
CYP1A2 inhibition - 0.8078 80.78%
CYP2C8 inhibition - 0.8892 88.92%
CYP inhibitory promiscuity - 0.9751 97.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.5313 53.13%
Eye corrosion - 0.9830 98.30%
Eye irritation - 0.8736 87.36%
Skin irritation - 0.7372 73.72%
Skin corrosion - 0.9286 92.86%
Ames mutagenesis - 0.6954 69.54%
Human Ether-a-go-go-Related Gene inhibition - 0.5256 52.56%
Micronuclear - 0.5500 55.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8829 88.29%
Respiratory toxicity + 0.7444 74.44%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6713 67.13%
Acute Oral Toxicity (c) III 0.6465 64.65%
Estrogen receptor binding - 0.5597 55.97%
Androgen receptor binding - 0.6393 63.93%
Thyroid receptor binding + 0.5181 51.81%
Glucocorticoid receptor binding - 0.4859 48.59%
Aromatase binding + 0.5820 58.20%
PPAR gamma + 0.5815 58.15%
Honey bee toxicity - 0.8763 87.63%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.8745 87.45%

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 98.48% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.87% 96.09%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 93.68% 90.71%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.94% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.66% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.67% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 85.03% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.99% 94.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.59% 99.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 83.97% 93.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.94% 92.08%

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 46886221
LOTUS LTS0101813
wikiData Q105004770