2,3,4-Trimethyltriacontane

Details

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Internal ID acbfd3bc-0448-487c-a443-2fb302ff35f4
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes > Branched alkanes
IUPAC Name 2,3,4-trimethyltriacontane
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCCCCCCCCC(C)C(C)C(C)C
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCCCCCCCCCC(C)C(C)C(C)C
InChI InChI=1S/C33H68/c1-6-7-8-9-10-11-12-13-14-15-16-17-18-19-20-21-22-23-24-25-26-27-28-29-30-32(4)33(5)31(2)3/h31-33H,6-30H2,1-5H3
InChI Key UIFMMGCTTVOBLD-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C33H68
Molecular Weight 464.90 g/mol
Exact Mass 464.532102169 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 17.20
Atomic LogP (AlogP) 12.69
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 27

Synonyms

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CHEBI:185354
DTXSID201311161
87538-96-3

2D Structure

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2D Structure of 2,3,4-Trimethyltriacontane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9924 99.24%
Caco-2 - 0.6271 62.71%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Lysosomes 0.4437 44.37%
OATP2B1 inhibitior - 0.8523 85.23%
OATP1B1 inhibitior + 0.9577 95.77%
OATP1B3 inhibitior + 0.9500 95.00%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.6049 60.49%
P-glycoprotein inhibitior - 0.6073 60.73%
P-glycoprotein substrate - 0.8405 84.05%
CYP3A4 substrate - 0.6790 67.90%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9872 98.72%
CYP2C9 inhibition - 0.9221 92.21%
CYP2C19 inhibition - 0.9470 94.70%
CYP2D6 inhibition - 0.9457 94.57%
CYP1A2 inhibition - 0.6898 68.98%
CYP2C8 inhibition - 0.9808 98.08%
CYP inhibitory promiscuity - 0.8241 82.41%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.6183 61.83%
Eye corrosion + 0.9891 98.91%
Eye irritation + 0.6930 69.30%
Skin irritation + 0.8188 81.88%
Skin corrosion - 0.9798 97.98%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7773 77.73%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.7507 75.07%
skin sensitisation + 0.9360 93.60%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.9674 96.74%
Mitochondrial toxicity + 0.9750 97.50%
Nephrotoxicity + 0.6964 69.64%
Acute Oral Toxicity (c) IV 0.4917 49.17%
Estrogen receptor binding + 0.5502 55.02%
Androgen receptor binding - 0.6288 62.88%
Thyroid receptor binding + 0.5749 57.49%
Glucocorticoid receptor binding - 0.5236 52.36%
Aromatase binding + 0.5397 53.97%
PPAR gamma + 0.6020 60.20%
Honey bee toxicity - 0.9819 98.19%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity + 0.7682 76.82%
Fish aquatic toxicity + 0.9819 98.19%

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
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 96.15% 92.86%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 95.34% 97.29%
CHEMBL2581 P07339 Cathepsin D 94.93% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.59% 92.08%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 92.12% 85.94%
CHEMBL2885 P07451 Carbonic anhydrase III 91.76% 87.45%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 91.28% 90.24%
CHEMBL1907 P15144 Aminopeptidase N 89.68% 93.31%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.26% 96.09%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.70% 93.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 87.61% 97.25%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 87.44% 95.17%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 87.18% 91.81%
CHEMBL230 P35354 Cyclooxygenase-2 87.17% 89.63%
CHEMBL2996 Q05655 Protein kinase C delta 86.00% 97.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.12% 99.17%
CHEMBL299 P17252 Protein kinase C alpha 84.50% 98.03%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.75% 90.71%
CHEMBL1907594 P30926 Neuronal acetylcholine receptor; alpha3/beta4 81.38% 97.23%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 81.00% 100.00%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 80.68% 96.47%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 80.63% 85.40%

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.
Solanum torvum

Cross-Links

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PubChem 129837279
LOTUS LTS0219898
wikiData Q105273345