14-Methyltritriacont-14-en-15-ol

Details

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Internal ID 4b3d896c-16b6-4079-b0c8-cfd1cd646314
Taxonomy Organic oxygen compounds > Organooxygen compounds > Enols
IUPAC Name 14-methyltritriacont-14-en-15-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H68O/c1-4-6-8-10-12-14-16-17-18-19-20-22-24-26-28-30-32-34(35)33(3)31-29-27-25-23-21-15-13-11-9-7-5-2/h35H,4-32H2,1-3H3
InChI Key FUEOUDDPJZETFT-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C34H68O
Molecular Weight 492.90 g/mol
Exact Mass 492.52701679 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 17.00
Atomic LogP (AlogP) 13.17
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 29

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 14-Methyltritriacont-14-en-15-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9930 99.30%
Caco-2 - 0.5613 56.13%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Lysosomes 0.3700 37.00%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.9022 90.22%
OATP1B3 inhibitior + 0.9422 94.22%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.5642 56.42%
P-glycoprotein inhibitior - 0.5858 58.58%
P-glycoprotein substrate - 0.8906 89.06%
CYP3A4 substrate - 0.6985 69.85%
CYP2C9 substrate - 0.7957 79.57%
CYP2D6 substrate - 0.7785 77.85%
CYP3A4 inhibition - 0.8287 82.87%
CYP2C9 inhibition - 0.8852 88.52%
CYP2C19 inhibition - 0.8850 88.50%
CYP2D6 inhibition - 0.9203 92.03%
CYP1A2 inhibition - 0.5000 50.00%
CYP2C8 inhibition - 0.9136 91.36%
CYP inhibitory promiscuity - 0.6466 64.66%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.6568 65.68%
Eye corrosion - 0.7131 71.31%
Eye irritation + 0.8265 82.65%
Skin irritation - 0.5316 53.16%
Skin corrosion - 0.9640 96.40%
Ames mutagenesis - 0.9477 94.77%
Human Ether-a-go-go-Related Gene inhibition - 0.6279 62.79%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7299 72.99%
skin sensitisation + 0.8980 89.80%
Respiratory toxicity - 0.9333 93.33%
Reproductive toxicity - 0.9526 95.26%
Mitochondrial toxicity - 0.7875 78.75%
Nephrotoxicity + 0.5326 53.26%
Acute Oral Toxicity (c) III 0.7000 70.00%
Estrogen receptor binding + 0.7342 73.42%
Androgen receptor binding - 0.4852 48.52%
Thyroid receptor binding + 0.5486 54.86%
Glucocorticoid receptor binding - 0.5547 55.47%
Aromatase binding - 0.5105 51.05%
PPAR gamma + 0.6937 69.37%
Honey bee toxicity - 0.9894 98.94%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.7390 73.90%
Fish aquatic toxicity + 0.9151 91.51%

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 94.70% 92.08%
CHEMBL2581 P07339 Cathepsin D 92.55% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.44% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.00% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 88.65% 89.63%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.85% 97.29%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 86.33% 95.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 82.69% 92.86%
CHEMBL2996 Q05655 Protein kinase C delta 81.70% 97.79%
CHEMBL2885 P07451 Carbonic anhydrase III 80.89% 87.45%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.85% 100.00%

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.
Dicliptera paniculata

Cross-Links

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PubChem 163193753
LOTUS LTS0090922
wikiData Q105001653