2-Pentadecylheptadec-2-enal

Details

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Internal ID 8212852e-bec3-4754-b9d1-8c9bc9dc20fe
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty aldehydes
IUPAC Name 2-pentadecylheptadec-2-enal
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C32H62O/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-32(31-33)30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h29,31H,3-28,30H2,1-2H3
InChI Key ZTWPAMLFNYHQIO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H62O
Molecular Weight 462.80 g/mol
Exact Mass 462.480066597 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 15.30
Atomic LogP (AlogP) 11.68
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 28

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Pentadecylheptadec-2-enal

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9950 99.50%
Caco-2 - 0.5444 54.44%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.3038 30.38%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.8489 84.89%
OATP1B3 inhibitior + 0.9267 92.67%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8346 83.46%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.9257 92.57%
CYP3A4 substrate - 0.6432 64.32%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.8311 83.11%
CYP3A4 inhibition - 0.9778 97.78%
CYP2C9 inhibition - 0.9349 93.49%
CYP2C19 inhibition - 0.9464 94.64%
CYP2D6 inhibition - 0.9487 94.87%
CYP1A2 inhibition + 0.5225 52.25%
CYP2C8 inhibition - 0.8787 87.87%
CYP inhibitory promiscuity - 0.6469 64.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Non-required 0.5861 58.61%
Eye corrosion + 0.8917 89.17%
Eye irritation + 0.8658 86.58%
Skin irritation + 0.8111 81.11%
Skin corrosion - 0.8916 89.16%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6444 64.44%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5413 54.13%
skin sensitisation + 0.9652 96.52%
Respiratory toxicity - 0.8444 84.44%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.4744 47.44%
Acute Oral Toxicity (c) III 0.8186 81.86%
Estrogen receptor binding + 0.6920 69.20%
Androgen receptor binding - 0.7664 76.64%
Thyroid receptor binding + 0.6429 64.29%
Glucocorticoid receptor binding - 0.6889 68.89%
Aromatase binding - 0.5978 59.78%
PPAR gamma + 0.6977 69.77%
Honey bee toxicity - 0.9897 98.97%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity + 0.8171 81.71%
Fish aquatic toxicity + 0.9876 98.76%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 96.07% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.88% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 93.71% 89.63%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 90.52% 85.94%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.45% 97.29%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.44% 92.86%
CHEMBL2581 P07339 Cathepsin D 87.32% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 85.58% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.75% 89.34%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.64% 91.81%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.09% 95.56%

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 85989834
LOTUS LTS0255268
wikiData Q104202783