10-Demethylsqualene

Details

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Internal ID 7ad2215c-7977-4374-9239-2a454a5fe67d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (6E,10E,14E,18E)-2,6,10,19,23-pentamethyltetracosa-2,6,10,14,18,22-hexaene
SMILES (Canonical) CC(=CCCC(=CCCC=CCCC=C(C)CCC=C(C)CCC=C(C)C)C)C
SMILES (Isomeric) CC(=CCC/C(=C/CC/C=C/CC/C=C(\C)/CC/C=C(\C)/CCC=C(C)C)/C)C
InChI InChI=1S/C29H48/c1-25(2)17-14-21-27(5)19-12-10-8-9-11-13-20-28(6)23-16-24-29(7)22-15-18-26(3)4/h8-9,17-20,24H,10-16,21-23H2,1-7H3/b9-8+,27-19+,28-20+,29-24+
InChI Key BBCQGYMUMKNTQE-BAIGTOHMSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C29H48
Molecular Weight 396.70 g/mol
Exact Mass 396.375601531 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 11.00
Atomic LogP (AlogP) 10.21
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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BBCQGYMUMKNTQE-BAIGTOHMSA-N
Q67879557

2D Structure

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2D Structure of 10-Demethylsqualene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 + 0.7392 73.92%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Nucleus 0.6684 66.84%
OATP2B1 inhibitior - 0.8556 85.56%
OATP1B1 inhibitior + 0.9165 91.65%
OATP1B3 inhibitior + 0.9380 93.80%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9258 92.58%
P-glycoprotein inhibitior + 0.6263 62.63%
P-glycoprotein substrate - 0.9703 97.03%
CYP3A4 substrate - 0.6445 64.45%
CYP2C9 substrate - 0.8202 82.02%
CYP2D6 substrate - 0.7454 74.54%
CYP3A4 inhibition - 0.9716 97.16%
CYP2C9 inhibition - 0.9099 90.99%
CYP2C19 inhibition - 0.9168 91.68%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.7354 73.54%
CYP2C8 inhibition - 0.9810 98.10%
CYP inhibitory promiscuity - 0.6923 69.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Warning 0.4712 47.12%
Eye corrosion + 0.7181 71.81%
Eye irritation - 0.5668 56.68%
Skin irritation + 0.8835 88.35%
Skin corrosion - 0.9656 96.56%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3642 36.42%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation + 0.9505 95.05%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.6195 61.95%
Acute Oral Toxicity (c) III 0.8971 89.71%
Estrogen receptor binding - 0.5000 50.00%
Androgen receptor binding - 0.8527 85.27%
Thyroid receptor binding + 0.6141 61.41%
Glucocorticoid receptor binding - 0.6040 60.40%
Aromatase binding - 0.6053 60.53%
PPAR gamma + 0.6326 63.26%
Honey bee toxicity - 0.8723 87.23%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9916 99.16%

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 95.39% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.16% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.38% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 83.23% 94.73%
CHEMBL2581 P07339 Cathepsin D 81.78% 98.95%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.00% 93.10%

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.
Jacobaea alpina subsp. samnitum
Panax ginseng

Cross-Links

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PubChem 5352455
NPASS NPC267374
LOTUS LTS0218019
wikiData Q67879557