31-Methyltritriacontan-1-ol

Details

Top
Internal ID 3707032a-f834-45ce-8cce-862218f44944
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohols
IUPAC Name 31-methyltritriacontan-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C34H70O/c1-3-34(2)32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35/h34-35H,3-33H2,1-2H3
InChI Key UANHRRDYCUUKPD-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C34H70O
Molecular Weight 494.90 g/mol
Exact Mass 494.54266685 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 16.80
Atomic LogP (AlogP) 12.34
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 31

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 31-Methyltritriacontan-1-ol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9918 99.18%
Caco-2 - 0.6140 61.40%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Lysosomes 0.6983 69.83%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9367 93.67%
OATP1B3 inhibitior + 0.8998 89.98%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.5917 59.17%
P-glycoprotein inhibitior - 0.7058 70.58%
P-glycoprotein substrate - 0.9045 90.45%
CYP3A4 substrate - 0.6915 69.15%
CYP2C9 substrate - 0.8468 84.68%
CYP2D6 substrate - 0.7359 73.59%
CYP3A4 inhibition - 0.8899 88.99%
CYP2C9 inhibition - 0.8723 87.23%
CYP2C19 inhibition - 0.9357 93.57%
CYP2D6 inhibition - 0.9192 91.92%
CYP1A2 inhibition - 0.5817 58.17%
CYP2C8 inhibition - 0.9786 97.86%
CYP inhibitory promiscuity - 0.8954 89.54%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.6900 69.00%
Carcinogenicity (trinary) Non-required 0.7594 75.94%
Eye corrosion + 0.6916 69.16%
Eye irritation + 0.5886 58.86%
Skin irritation - 0.5805 58.05%
Skin corrosion - 0.9838 98.38%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6136 61.36%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5541 55.41%
skin sensitisation + 0.9176 91.76%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9750 97.50%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.8840 88.40%
Estrogen receptor binding + 0.6787 67.87%
Androgen receptor binding - 0.7622 76.22%
Thyroid receptor binding + 0.6803 68.03%
Glucocorticoid receptor binding - 0.5566 55.66%
Aromatase binding - 0.5180 51.80%
PPAR gamma + 0.5750 57.50%
Honey bee toxicity - 0.9878 98.78%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity - 0.8145 81.45%
Fish aquatic toxicity + 0.7438 74.38%

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
CHEMBL2885 P07451 Carbonic anhydrase III 95.58% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.38% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 93.31% 97.29%
CHEMBL2581 P07339 Cathepsin D 90.65% 98.95%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 89.04% 92.86%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.41% 99.17%
CHEMBL226 P30542 Adenosine A1 receptor 82.75% 95.93%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.41% 93.56%

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.
Cissus quadrangularis

Cross-Links

Top
PubChem 14825494
LOTUS LTS0245501
wikiData Q105268933