(25S)-25-hydroxydotriacontan-3-one

Details

Top
Internal ID b934625e-8a4d-4097-a4a4-f1cf2b2ec586
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name (25S)-25-hydroxydotriacontan-3-one
SMILES (Canonical) CCCCCCCC(CCCCCCCCCCCCCCCCCCCCCC(=O)CC)O
SMILES (Isomeric) CCCCCCC[C@@H](CCCCCCCCCCCCCCCCCCCCCC(=O)CC)O
InChI InChI=1S/C32H64O2/c1-3-5-6-22-26-29-32(34)30-27-24-21-19-17-15-13-11-9-7-8-10-12-14-16-18-20-23-25-28-31(33)4-2/h32,34H,3-30H2,1-2H3/t32-/m0/s1
InChI Key PMWIFCAKOPRVIG-YTTGMZPUSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C32H64O2
Molecular Weight 480.80 g/mol
Exact Mass 480.49063128 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 13.40
Atomic LogP (AlogP) 10.88
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 29

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of (25S)-25-hydroxydotriacontan-3-one

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 - 0.6975 69.75%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.6771 67.71%
OATP2B1 inhibitior - 0.8525 85.25%
OATP1B1 inhibitior + 0.9420 94.20%
OATP1B3 inhibitior + 0.8581 85.81%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.6851 68.51%
P-glycoprotein inhibitior - 0.6111 61.11%
P-glycoprotein substrate - 0.8262 82.62%
CYP3A4 substrate - 0.6205 62.05%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7417 74.17%
CYP3A4 inhibition - 0.9212 92.12%
CYP2C9 inhibition - 0.8886 88.86%
CYP2C19 inhibition - 0.9387 93.87%
CYP2D6 inhibition - 0.9213 92.13%
CYP1A2 inhibition + 0.7273 72.73%
CYP2C8 inhibition - 0.9457 94.57%
CYP inhibitory promiscuity - 0.9039 90.39%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6700 67.00%
Carcinogenicity (trinary) Non-required 0.7446 74.46%
Eye corrosion + 0.9052 90.52%
Eye irritation + 0.7920 79.20%
Skin irritation - 0.5658 56.58%
Skin corrosion - 0.8327 83.27%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6199 61.99%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5183 51.83%
skin sensitisation + 0.9170 91.70%
Respiratory toxicity - 0.8889 88.89%
Reproductive toxicity - 0.7518 75.18%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.4780 47.80%
Acute Oral Toxicity (c) III 0.8151 81.51%
Estrogen receptor binding - 0.5177 51.77%
Androgen receptor binding - 0.8479 84.79%
Thyroid receptor binding + 0.5463 54.63%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.6597 65.97%
PPAR gamma + 0.6149 61.49%
Honey bee toxicity - 0.9821 98.21%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.6493 64.93%
Fish aquatic toxicity + 0.7801 78.01%

Targets

Top

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 96.42% 96.09%
CHEMBL2581 P07339 Cathepsin D 96.23% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 95.69% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 94.47% 99.17%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 94.04% 85.94%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 90.64% 92.08%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 89.97% 95.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.54% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 88.30% 89.63%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.33% 97.25%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 85.68% 91.81%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.22% 93.56%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 84.69% 100.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 84.48% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.45% 96.95%
CHEMBL1907 P15144 Aminopeptidase N 83.67% 93.31%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 81.80% 97.21%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.83% 100.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 80.12% 90.71%
CHEMBL4040 P28482 MAP kinase ERK2 80.09% 83.82%
CHEMBL299 P17252 Protein kinase C alpha 80.09% 98.03%

Plants that contains it

Top
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.
Duboisia myoporoides

Cross-Links

Top
PubChem 162945216
LOTUS LTS0147617
wikiData Q105211778