Concentricol

Details

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Internal ID e658926b-9e9a-4c7a-b078-fb3578a9d0c5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (2E,10E,14E,22E)-2,6,10,15,19,23-hexamethyltetracosa-2,10,14,22-tetraene-1,6,7,18,19,24-hexol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H54O6/c1-23(15-17-27(33)29(5,35)19-9-13-25(3)21-31)11-7-8-12-24(2)16-18-28(34)30(6,36)20-10-14-26(4)22-32/h11-14,27-28,31-36H,7-10,15-22H2,1-6H3/b23-11+,24-12+,25-13+,26-14+
InChI Key VZNMYFXGBPEORA-VUHAMLAFSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H54O6
Molecular Weight 510.70 g/mol
Exact Mass 510.39203944 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 4.70
Atomic LogP (AlogP) 4.88
H-Bond Acceptor 6
H-Bond Donor 6
Rotatable Bonds 19

Synonyms

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(2E,10E,14E,22E)-2,6,10,15,19,23-hexamethyltetracosa-2,10,14,22-tetraene-1,6,7,18,19,24-hexol

2D Structure

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2D Structure of Concentricol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8848 88.48%
Caco-2 - 0.7774 77.74%
Blood Brain Barrier + 0.6385 63.85%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.6049 60.49%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9299 92.99%
OATP1B3 inhibitior + 0.9424 94.24%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.6791 67.91%
BSEP inhibitior + 0.9189 91.89%
P-glycoprotein inhibitior + 0.5780 57.80%
P-glycoprotein substrate - 0.8279 82.79%
CYP3A4 substrate - 0.5412 54.12%
CYP2C9 substrate - 0.8127 81.27%
CYP2D6 substrate - 0.7783 77.83%
CYP3A4 inhibition - 0.7745 77.45%
CYP2C9 inhibition - 0.8591 85.91%
CYP2C19 inhibition - 0.8588 85.88%
CYP2D6 inhibition - 0.9136 91.36%
CYP1A2 inhibition - 0.8470 84.70%
CYP2C8 inhibition - 0.9415 94.15%
CYP inhibitory promiscuity - 0.9362 93.62%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.7304 73.04%
Eye corrosion - 0.9646 96.46%
Eye irritation - 0.8784 87.84%
Skin irritation - 0.7160 71.60%
Skin corrosion - 0.9827 98.27%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3659 36.59%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.6500 65.00%
skin sensitisation - 0.5860 58.60%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.8667 86.67%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity + 0.5150 51.50%
Acute Oral Toxicity (c) IV 0.4900 49.00%
Estrogen receptor binding + 0.6813 68.13%
Androgen receptor binding - 0.5748 57.48%
Thyroid receptor binding + 0.5825 58.25%
Glucocorticoid receptor binding + 0.6194 61.94%
Aromatase binding + 0.5933 59.33%
PPAR gamma + 0.6585 65.85%
Honey bee toxicity - 0.8309 83.09%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.7207 72.07%

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 93.83% 98.95%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 90.16% 97.29%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.11% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 87.07% 94.73%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 86.84% 85.14%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.81% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.57% 99.17%
CHEMBL1907 P15144 Aminopeptidase N 82.33% 93.31%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.92% 89.34%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.23% 91.11%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.80% 96.90%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 12041832
LOTUS LTS0273567
wikiData Q77369764