17-Methylnonadecylbenzene

Details

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Internal ID 487c9796-8e52-4c1c-afdd-36bb4f866836
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name 17-methylnonadecylbenzene
SMILES (Canonical) CCC(C)CCCCCCCCCCCCCCCCC1=CC=CC=C1
SMILES (Isomeric) CCC(C)CCCCCCCCCCCCCCCCC1=CC=CC=C1
InChI InChI=1S/C26H46/c1-3-25(2)21-17-14-12-10-8-6-4-5-7-9-11-13-15-18-22-26-23-19-16-20-24-26/h16,19-20,23-25H,3-15,17-18,21-22H2,1-2H3
InChI Key NONIUUZEGFKBED-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H46
Molecular Weight 358.60 g/mol
Exact Mass 358.359951467 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 12.80
Atomic LogP (AlogP) 9.13
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 18

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 17-Methylnonadecylbenzene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9961 99.61%
Caco-2 + 0.7371 73.71%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.5187 51.87%
OATP2B1 inhibitior - 0.8544 85.44%
OATP1B1 inhibitior + 0.9068 90.68%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7902 79.02%
P-glycoprotein inhibitior - 0.6325 63.25%
P-glycoprotein substrate - 0.6089 60.89%
CYP3A4 substrate - 0.6049 60.49%
CYP2C9 substrate - 0.8214 82.14%
CYP2D6 substrate + 0.3542 35.42%
CYP3A4 inhibition - 0.9532 95.32%
CYP2C9 inhibition - 0.9126 91.26%
CYP2C19 inhibition - 0.8998 89.98%
CYP2D6 inhibition - 0.8645 86.45%
CYP1A2 inhibition - 0.5996 59.96%
CYP2C8 inhibition - 0.8385 83.85%
CYP inhibitory promiscuity - 0.6643 66.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.5389 53.89%
Eye corrosion + 0.9561 95.61%
Eye irritation + 0.7584 75.84%
Skin irritation + 0.6425 64.25%
Skin corrosion - 0.9659 96.59%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7130 71.30%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5265 52.65%
skin sensitisation + 0.9274 92.74%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.7740 77.40%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6899 68.99%
Acute Oral Toxicity (c) III 0.7630 76.30%
Estrogen receptor binding + 0.7695 76.95%
Androgen receptor binding - 0.6266 62.66%
Thyroid receptor binding + 0.6386 63.86%
Glucocorticoid receptor binding - 0.7352 73.52%
Aromatase binding - 0.5558 55.58%
PPAR gamma - 0.4947 49.47%
Honey bee toxicity - 0.9668 96.68%
Biodegradation + 0.7000 70.00%
Crustacea aquatic toxicity + 0.7000 70.00%
Fish aquatic toxicity + 0.9969 99.69%

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
CHEMBL2581 P07339 Cathepsin D 98.43% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.63% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 92.52% 94.62%
CHEMBL221 P23219 Cyclooxygenase-1 90.59% 90.17%
CHEMBL1907 P15144 Aminopeptidase N 87.98% 93.31%
CHEMBL3401 O75469 Pregnane X receptor 87.90% 94.73%
CHEMBL2885 P07451 Carbonic anhydrase III 84.85% 87.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.47% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.36% 86.33%
CHEMBL5939 Q9NZ08 Endoplasmic reticulum aminopeptidase 1 84.13% 100.00%
CHEMBL5805 Q9NR97 Toll-like receptor 8 83.91% 96.25%
CHEMBL3902 P09211 Glutathione S-transferase Pi 82.87% 93.81%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 81.96% 92.08%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 81.26% 94.08%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.03% 93.56%

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.
Tridax procumbens

Cross-Links

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PubChem 85550305
LOTUS LTS0246544
wikiData Q105182662