Tritetracontane

Details

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Internal ID b12fbb56-5dca-425e-8163-ec7ef33e9350
Taxonomy Hydrocarbons > Saturated hydrocarbons > Alkanes
IUPAC Name tritetracontane
SMILES (Canonical) CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
SMILES (Isomeric) CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC
InChI InChI=1S/C43H88/c1-3-5-7-9-11-13-15-17-19-21-23-25-27-29-31-33-35-37-39-41-43-42-40-38-36-34-32-30-28-26-24-22-20-18-16-14-12-10-8-6-4-2/h3-43H2,1-2H3
InChI Key PKBVGJFKBPLWOD-UHFFFAOYSA-N
Popularity 28 references in papers

Physical and Chemical Properties

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Molecular Formula C43H88
Molecular Weight 605.20 g/mol
Exact Mass 604.68860281 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 22.90
Atomic LogP (AlogP) 17.02
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 40

Synonyms

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7098-21-7
DTXSID90334942
PKBVGJFKBPLWOD-UHFFFAOYSA-N
62479D2D-191F-4EBB-85E5-9BFEAB9BB03C
Q18456290

2D Structure

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2D Structure of Tritetracontane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.5166 51.66%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Lysosomes 0.5981 59.81%
OATP2B1 inhibitior - 0.8513 85.13%
OATP1B1 inhibitior + 0.9552 95.52%
OATP1B3 inhibitior + 0.9429 94.29%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5479 54.79%
P-glycoprotein inhibitior - 0.7233 72.33%
P-glycoprotein substrate - 0.9516 95.16%
CYP3A4 substrate - 0.7947 79.47%
CYP2C9 substrate - 0.8415 84.15%
CYP2D6 substrate - 0.7215 72.15%
CYP3A4 inhibition - 0.9877 98.77%
CYP2C9 inhibition - 0.9349 93.49%
CYP2C19 inhibition - 0.9540 95.40%
CYP2D6 inhibition - 0.9373 93.73%
CYP1A2 inhibition - 0.6175 61.75%
CYP2C8 inhibition - 0.9765 97.65%
CYP inhibitory promiscuity - 0.8149 81.49%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5900 59.00%
Carcinogenicity (trinary) Non-required 0.6328 63.28%
Eye corrosion + 0.9946 99.46%
Eye irritation + 0.9439 94.39%
Skin irritation + 0.8623 86.23%
Skin corrosion - 0.9874 98.74%
Ames mutagenesis - 1.0000 100.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7800 78.00%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.8836 88.36%
skin sensitisation + 0.9563 95.63%
Respiratory toxicity - 1.0000 100.00%
Reproductive toxicity - 0.6948 69.48%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity + 0.6552 65.52%
Acute Oral Toxicity (c) III 0.6143 61.43%
Estrogen receptor binding + 0.6567 65.67%
Androgen receptor binding - 0.8473 84.73%
Thyroid receptor binding - 0.6090 60.90%
Glucocorticoid receptor binding - 0.7087 70.87%
Aromatase binding - 0.5593 55.93%
PPAR gamma - 0.6033 60.33%
Honey bee toxicity - 0.9939 99.39%
Biodegradation + 1.0000 100.00%
Crustacea aquatic toxicity + 0.8690 86.90%
Fish aquatic toxicity + 0.9770 97.70%

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 94.23% 92.08%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 91.92% 92.86%
CHEMBL230 P35354 Cyclooxygenase-2 91.78% 89.63%
CHEMBL2581 P07339 Cathepsin D 89.44% 98.95%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 88.64% 91.81%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 88.59% 97.29%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.93% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 86.52% 87.45%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.15% 85.94%
CHEMBL4462 Q8IXJ6 NAD-dependent deacetylase sirtuin 2 83.58% 90.24%
CHEMBL2996 Q05655 Protein kinase C delta 83.44% 97.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.77% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 81.78% 93.31%

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.
Arachis hypogaea
Astilbe rubra
Combretum indicum
Senecio cerberoanus
Terminalia chebula

Cross-Links

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PubChem 522398
NPASS NPC294035
LOTUS LTS0155649
wikiData Q18456290