(6S,10R,15S,19R)-2,6,10,15,19,23-hexamethyltetracosane

Details

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Internal ID 61ed5a04-385b-4c08-aabc-e79e071d1343
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (6S,10R,15S,19R)-2,6,10,15,19,23-hexamethyltetracosane
SMILES (Canonical) CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C
SMILES (Isomeric) C[C@H](CCCC[C@H](C)CCC[C@H](C)CCCC(C)C)CCC[C@@H](C)CCCC(C)C
InChI InChI=1S/C30H62/c1-25(2)15-11-19-29(7)23-13-21-27(5)17-9-10-18-28(6)22-14-24-30(8)20-12-16-26(3)4/h25-30H,9-24H2,1-8H3/t27-,28+,29+,30-
InChI Key PRAKJMSDJKAYCZ-LPOKLPNDSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C30H62
Molecular Weight 422.80 g/mol
Exact Mass 422.485151978 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 14.70
Atomic LogP (AlogP) 11.08
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 21

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6S,10R,15S,19R)-2,6,10,15,19,23-hexamethyltetracosane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9890 98.90%
Caco-2 - 0.5134 51.34%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.4160 41.60%
OATP2B1 inhibitior - 0.8550 85.50%
OATP1B1 inhibitior + 0.9790 97.90%
OATP1B3 inhibitior + 0.9508 95.08%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.5726 57.26%
P-glycoprotein inhibitior - 0.6019 60.19%
P-glycoprotein substrate - 0.8770 87.70%
CYP3A4 substrate - 0.7141 71.41%
CYP2C9 substrate - 0.8153 81.53%
CYP2D6 substrate - 0.7243 72.43%
CYP3A4 inhibition - 0.9879 98.79%
CYP2C9 inhibition - 0.9393 93.93%
CYP2C19 inhibition - 0.9537 95.37%
CYP2D6 inhibition - 0.9595 95.95%
CYP1A2 inhibition - 0.7915 79.15%
CYP2C8 inhibition - 0.9946 99.46%
CYP inhibitory promiscuity - 0.8953 89.53%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6061 60.61%
Eye corrosion + 0.9879 98.79%
Eye irritation + 0.9629 96.29%
Skin irritation + 0.8683 86.83%
Skin corrosion - 0.9821 98.21%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6909 69.09%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.6302 63.02%
skin sensitisation + 0.9397 93.97%
Respiratory toxicity + 0.8778 87.78%
Reproductive toxicity - 0.9689 96.89%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity - 0.5943 59.43%
Acute Oral Toxicity (c) III 0.6311 63.11%
Estrogen receptor binding + 0.5942 59.42%
Androgen receptor binding - 0.8597 85.97%
Thyroid receptor binding - 0.5338 53.38%
Glucocorticoid receptor binding - 0.5765 57.65%
Aromatase binding + 0.6235 62.35%
PPAR gamma - 0.4908 49.08%
Honey bee toxicity - 0.9703 97.03%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9700 97.00%

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
CHEMBL1907 P15144 Aminopeptidase N 89.85% 93.31%
CHEMBL2581 P07339 Cathepsin D 88.71% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.02% 96.09%
CHEMBL2885 P07451 Carbonic anhydrase III 84.49% 87.45%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 83.76% 97.29%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.58% 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.
Chaenomeles sinensis
Porella cordaeana
Tessaria integrifolia

Cross-Links

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PubChem 73416503
NPASS NPC133877
LOTUS LTS0234656
wikiData Q105213569