6,10,14,18,22,26,30,34-Octamethylpentatriaconta-5,9,13,17,21,25,29,33-octaen-2-one

Details

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Internal ID f2a57195-12f2-4809-a06c-1957256c1c95
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids
IUPAC Name 6,10,14,18,22,26,30,34-octamethylpentatriaconta-5,9,13,17,21,25,29,33-octaen-2-one
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=O)C)C)C)C)C)C)C)C)C
SMILES (Isomeric) CC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=CCCC(=O)C)C)C)C)C)C)C)C)C
InChI InChI=1S/C43H70O/c1-35(2)19-11-20-36(3)21-12-22-37(4)23-13-24-38(5)25-14-26-39(6)27-15-28-40(7)29-16-30-41(8)31-17-32-42(9)33-18-34-43(10)44/h19,21,23,25,27,29,31,33H,11-18,20,22,24,26,28,30,32,34H2,1-10H3
InChI Key RPUKUBKVRRNJDI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C43H70O
Molecular Weight 603.00 g/mol
Exact Mass 602.54266685 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 14.80
Atomic LogP (AlogP) 14.41
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 24

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6,10,14,18,22,26,30,34-Octamethylpentatriaconta-5,9,13,17,21,25,29,33-octaen-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9927 99.27%
Caco-2 - 0.7538 75.38%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Nucleus 0.4369 43.69%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.9491 94.91%
OATP1B3 inhibitior + 0.9376 93.76%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9584 95.84%
P-glycoprotein inhibitior + 0.7447 74.47%
P-glycoprotein substrate - 0.9782 97.82%
CYP3A4 substrate - 0.6536 65.36%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7774 77.74%
CYP3A4 inhibition - 0.9623 96.23%
CYP2C9 inhibition - 0.9086 90.86%
CYP2C19 inhibition - 0.9062 90.62%
CYP2D6 inhibition - 0.9612 96.12%
CYP1A2 inhibition - 0.5346 53.46%
CYP2C8 inhibition - 0.9859 98.59%
CYP inhibitory promiscuity - 0.7543 75.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6029 60.29%
Eye corrosion + 0.6517 65.17%
Eye irritation - 0.8336 83.36%
Skin irritation + 0.8176 81.76%
Skin corrosion - 0.9611 96.11%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6818 68.18%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5375 53.75%
skin sensitisation + 0.9472 94.72%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity - 0.9889 98.89%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.6592 65.92%
Acute Oral Toxicity (c) III 0.8221 82.21%
Estrogen receptor binding + 0.7391 73.91%
Androgen receptor binding - 0.8537 85.37%
Thyroid receptor binding - 0.5515 55.15%
Glucocorticoid receptor binding + 0.5576 55.76%
Aromatase binding - 0.5441 54.41%
PPAR gamma + 0.6580 65.80%
Honey bee toxicity - 0.9198 91.98%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity + 0.9240 92.40%

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 93.15% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.85% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.93% 99.17%
CHEMBL2581 P07339 Cathepsin D 82.51% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 82.25% 94.73%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.61% 89.34%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.30% 96.95%

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.
Nicotiana tabacum

Cross-Links

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PubChem 54279504
LOTUS LTS0255289
wikiData Q105243030