3-tricos-16-enyl-1H-pyrrole-2-carbaldehyde

Details

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Internal ID 5cae8a65-0105-4a4a-89cf-449ea3ee2aed
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Aryl-aldehydes
IUPAC Name 3-tricos-16-enyl-1H-pyrrole-2-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H49NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-27-24-25-29-28(27)26-30/h7-8,24-26,29H,2-6,9-23H2,1H3
InChI Key UPBUBFBSVVKBHN-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H49NO
Molecular Weight 415.70 g/mol
Exact Mass 415.381415187 g/mol
Topological Polar Surface Area (TPSA) 32.90 Ų
XlogP 11.70
Atomic LogP (AlogP) 9.36
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 22

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-tricos-16-enyl-1H-pyrrole-2-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 - 0.5995 59.95%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.3690 36.90%
OATP2B1 inhibitior - 0.8581 85.81%
OATP1B1 inhibitior + 0.8274 82.74%
OATP1B3 inhibitior + 0.9356 93.56%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.7351 73.51%
P-glycoprotein inhibitior - 0.5260 52.60%
P-glycoprotein substrate - 0.7284 72.84%
CYP3A4 substrate - 0.5434 54.34%
CYP2C9 substrate - 0.6070 60.70%
CYP2D6 substrate - 0.8058 80.58%
CYP3A4 inhibition - 0.8848 88.48%
CYP2C9 inhibition - 0.5211 52.11%
CYP2C19 inhibition + 0.6506 65.06%
CYP2D6 inhibition - 0.8509 85.09%
CYP1A2 inhibition + 0.8594 85.94%
CYP2C8 inhibition - 0.6028 60.28%
CYP inhibitory promiscuity + 0.7671 76.71%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6235 62.35%
Eye corrosion - 0.9109 91.09%
Eye irritation - 0.5925 59.25%
Skin irritation - 0.5982 59.82%
Skin corrosion - 0.8447 84.47%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7824 78.24%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.7141 71.41%
skin sensitisation - 0.6669 66.69%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.6333 63.33%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.5693 56.93%
Acute Oral Toxicity (c) III 0.6713 67.13%
Estrogen receptor binding + 0.6549 65.49%
Androgen receptor binding - 0.6236 62.36%
Thyroid receptor binding + 0.5944 59.44%
Glucocorticoid receptor binding - 0.4795 47.95%
Aromatase binding - 0.5973 59.73%
PPAR gamma + 0.5411 54.11%
Honey bee toxicity - 0.9718 97.18%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.8400 84.00%
Fish aquatic toxicity + 0.9796 97.96%

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 97.32% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.80% 92.08%
CHEMBL2996 Q05655 Protein kinase C delta 92.86% 97.79%
CHEMBL230 P35354 Cyclooxygenase-2 92.54% 89.63%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.28% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.79% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.40% 91.11%
CHEMBL1781 P11387 DNA topoisomerase I 90.34% 97.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.37% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 88.25% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.29% 94.45%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 84.13% 92.86%
CHEMBL255 P29275 Adenosine A2b receptor 83.38% 98.59%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.21% 91.81%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 81.96% 92.88%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.55% 96.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.19% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.92% 96.00%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.64% 93.99%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.24% 100.00%

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 163038430
LOTUS LTS0035005
wikiData Q105276692