21-Hydroxytetracontan-20-one

Details

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Internal ID d3fec833-257b-4fe0-bfb3-88bb8a6661b7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols > Long-chain fatty alcohols
IUPAC Name 21-hydroxytetracontan-20-one
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCC(C(=O)CCCCCCCCCCCCCCCCCCC)O
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCCC(C(=O)CCCCCCCCCCCCCCCCCCC)O
InChI InChI=1S/C40H80O2/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-39(41)40(42)38-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h39,41H,3-38H2,1-2H3
InChI Key FUXWJXFNCIATEB-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C40H80O2
Molecular Weight 593.10 g/mol
Exact Mass 592.61583179 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 18.70
Atomic LogP (AlogP) 14.00
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 37

Synonyms

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18216-95-0
DTXSID50775534

2D Structure

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2D Structure of 21-Hydroxytetracontan-20-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9932 99.32%
Caco-2 - 0.7185 71.85%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.6776 67.76%
OATP2B1 inhibitior - 0.8516 85.16%
OATP1B1 inhibitior + 0.9402 94.02%
OATP1B3 inhibitior + 0.8664 86.64%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6683 66.83%
P-glycoprotein inhibitior - 0.5367 53.67%
P-glycoprotein substrate - 0.8348 83.48%
CYP3A4 substrate - 0.6361 63.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7417 74.17%
CYP3A4 inhibition - 0.9282 92.82%
CYP2C9 inhibition - 0.8769 87.69%
CYP2C19 inhibition - 0.9098 90.98%
CYP2D6 inhibition - 0.9194 91.94%
CYP1A2 inhibition + 0.6776 67.76%
CYP2C8 inhibition - 0.9703 97.03%
CYP inhibitory promiscuity - 0.9161 91.61%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.7428 74.28%
Eye corrosion + 0.8827 88.27%
Eye irritation + 0.7807 78.07%
Skin irritation + 0.5197 51.97%
Skin corrosion - 0.8737 87.37%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5876 58.76%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5192 51.92%
skin sensitisation + 0.9134 91.34%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.7371 73.71%
Mitochondrial toxicity - 0.6625 66.25%
Nephrotoxicity - 0.5932 59.32%
Acute Oral Toxicity (c) III 0.6426 64.26%
Estrogen receptor binding + 0.6059 60.59%
Androgen receptor binding - 0.7694 76.94%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.4813 48.13%
Aromatase binding - 0.6723 67.23%
PPAR gamma + 0.5995 59.95%
Honey bee toxicity - 0.9905 99.05%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.6793 67.93%
Fish aquatic toxicity + 0.7201 72.01%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.85% 96.09%
CHEMBL2581 P07339 Cathepsin D 95.68% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.22% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 94.72% 97.29%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 91.58% 85.94%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.39% 92.86%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.01% 92.08%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.85% 97.25%
CHEMBL230 P35354 Cyclooxygenase-2 87.74% 89.63%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 87.06% 91.81%
CHEMBL299 P17252 Protein kinase C alpha 86.09% 98.03%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.37% 93.56%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 85.06% 95.17%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.29% 100.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.10% 100.00%
CHEMBL1907 P15144 Aminopeptidase N 82.37% 93.31%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.93% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.10% 90.71%

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.
Curculigo orchioides

Cross-Links

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PubChem 71349693
LOTUS LTS0125976
wikiData Q82737026