Mycalazal 14

Details

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Internal ID 17955afb-35d3-48c7-aed4-586f9f6d08af
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Aryl-aldehydes
IUPAC Name 5-tetradecyl-1H-pyrrole-2-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H33NO/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-18-15-16-19(17-21)20-18/h15-17,20H,2-14H2,1H3
InChI Key VRWBBCYCUOMPBF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H33NO
Molecular Weight 291.50 g/mol
Exact Mass 291.256214676 g/mol
Topological Polar Surface Area (TPSA) 32.90 Ų
XlogP 7.70
Atomic LogP (AlogP) 6.07
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

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CHEMBL1080266
BDBM50481881

2D Structure

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2D Structure of Mycalazal 14

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 + 0.6858 68.58%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.6446 64.46%
OATP2B1 inhibitior - 0.8570 85.70%
OATP1B1 inhibitior + 0.8617 86.17%
OATP1B3 inhibitior + 0.9386 93.86%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.5646 56.46%
P-glycoprotein inhibitior - 0.8688 86.88%
P-glycoprotein substrate - 0.7660 76.60%
CYP3A4 substrate - 0.6011 60.11%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7474 74.74%
CYP3A4 inhibition - 0.9503 95.03%
CYP2C9 inhibition - 0.7412 74.12%
CYP2C19 inhibition + 0.5098 50.98%
CYP2D6 inhibition - 0.8287 82.87%
CYP1A2 inhibition + 0.6622 66.22%
CYP2C8 inhibition - 0.8163 81.63%
CYP inhibitory promiscuity - 0.5784 57.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.6843 68.43%
Eye corrosion - 0.8393 83.93%
Eye irritation + 0.6296 62.96%
Skin irritation + 0.4893 48.93%
Skin corrosion - 0.6530 65.30%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8950 89.50%
Micronuclear - 0.7500 75.00%
Hepatotoxicity + 0.6183 61.83%
skin sensitisation - 0.7749 77.49%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity + 0.5822 58.22%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity + 0.6050 60.50%
Acute Oral Toxicity (c) III 0.6514 65.14%
Estrogen receptor binding + 0.5620 56.20%
Androgen receptor binding - 0.7631 76.31%
Thyroid receptor binding + 0.7462 74.62%
Glucocorticoid receptor binding - 0.5668 56.68%
Aromatase binding - 0.6849 68.49%
PPAR gamma + 0.8008 80.08%
Honey bee toxicity - 0.9850 98.50%
Biodegradation + 0.5750 57.50%
Crustacea aquatic toxicity + 0.8272 82.72%
Fish aquatic toxicity + 0.8262 82.62%

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 96.05% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.21% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.21% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.51% 95.56%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 88.09% 92.86%
CHEMBL255 P29275 Adenosine A2b receptor 87.96% 98.59%
CHEMBL3401 O75469 Pregnane X receptor 87.02% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.35% 94.45%
CHEMBL230 P35354 Cyclooxygenase-2 85.62% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 85.28% 97.25%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.77% 99.17%
CHEMBL1781 P11387 DNA topoisomerase I 82.57% 97.00%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.96% 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 44605144
LOTUS LTS0156687
wikiData Q105291998