4-(3,7-dimethylocta-2,6-dienyl)-1H-pyrrole-2-carboxylic acid

Details

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Internal ID 057ef646-4b0b-4af7-837b-6eca2ed93a24
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Aromatic monoterpenoids
IUPAC Name 4-(3,7-dimethylocta-2,6-dienyl)-1H-pyrrole-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H21NO2/c1-11(2)5-4-6-12(3)7-8-13-9-14(15(17)18)16-10-13/h5,7,9-10,16H,4,6,8H2,1-3H3,(H,17,18)
InChI Key UEQIBCOZMSTCSW-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C15H21NO2
Molecular Weight 247.33 g/mol
Exact Mass 247.157228913 g/mol
Topological Polar Surface Area (TPSA) 53.10 Ų
XlogP 4.40
Atomic LogP (AlogP) 3.95
H-Bond Acceptor 1
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-(3,7-dimethylocta-2,6-dienyl)-1H-pyrrole-2-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.6244 62.44%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.4234 42.34%
OATP2B1 inhibitior - 0.8585 85.85%
OATP1B1 inhibitior + 0.9060 90.60%
OATP1B3 inhibitior + 0.9179 91.79%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.9514 95.14%
P-glycoprotein substrate - 0.8800 88.00%
CYP3A4 substrate - 0.5976 59.76%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate - 0.8857 88.57%
CYP3A4 inhibition - 0.7537 75.37%
CYP2C9 inhibition - 0.6226 62.26%
CYP2C19 inhibition - 0.7304 73.04%
CYP2D6 inhibition - 0.8866 88.66%
CYP1A2 inhibition - 0.5261 52.61%
CYP2C8 inhibition - 0.8710 87.10%
CYP inhibitory promiscuity - 0.6447 64.47%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.6099 60.99%
Eye corrosion - 0.9771 97.71%
Eye irritation - 0.6642 66.42%
Skin irritation - 0.7165 71.65%
Skin corrosion - 0.9288 92.88%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5305 53.05%
Micronuclear - 0.7000 70.00%
Hepatotoxicity - 0.5448 54.48%
skin sensitisation - 0.7478 74.78%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.5487 54.87%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8014 80.14%
Acute Oral Toxicity (c) III 0.5996 59.96%
Estrogen receptor binding - 0.5360 53.60%
Androgen receptor binding - 0.8619 86.19%
Thyroid receptor binding - 0.5309 53.09%
Glucocorticoid receptor binding - 0.7070 70.70%
Aromatase binding + 0.5383 53.83%
PPAR gamma + 0.7940 79.40%
Honey bee toxicity - 0.9206 92.06%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.9792 97.92%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.27% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.80% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.75% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.91% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.84% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 89.36% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 86.53% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.00% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 83.76% 90.17%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.63% 93.00%

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 4997
LOTUS LTS0273586
wikiData Q104198120