2,2-Dimethyl-3-(3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaenyl)oxirane

Details

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Internal ID 3c6bc19a-e5b5-4558-af2e-2b5e4c676e59
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name 2,2-dimethyl-3-(3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaenyl)oxirane
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC1C(O1)(C)C)C)C)C
SMILES (Isomeric) CC(=CCCC(=CCCC(=CCCC=C(C)CCC=C(C)CCC1C(O1)(C)C)C)C)C
InChI InChI=1S/C30H50O/c1-24(2)14-11-17-27(5)20-12-18-25(3)15-9-10-16-26(4)19-13-21-28(6)22-23-29-30(7,8)31-29/h14-16,20-21,29H,9-13,17-19,22-23H2,1-8H3
InChI Key QYIMSPSDBYKPPY-UHFFFAOYSA-N
Popularity 79 references in papers

Physical and Chemical Properties

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Molecular Formula C30H50O
Molecular Weight 426.70 g/mol
Exact Mass 426.386166214 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 10.30
Atomic LogP (AlogP) 9.82
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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54910-48-4
2,2-dimethyl-3-(3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaen-1-yl)oxirane
2,2-dimethyl-3-(3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaenyl)oxirane
FT-0770470

2D Structure

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2D Structure of 2,2-Dimethyl-3-(3,7,12,16,20-pentamethylhenicosa-3,7,11,15,19-pentaenyl)oxirane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9880 98.80%
Caco-2 + 0.5771 57.71%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Lysosomes 0.3590 35.90%
OATP2B1 inhibitior - 0.8567 85.67%
OATP1B1 inhibitior + 0.9183 91.83%
OATP1B3 inhibitior + 0.9258 92.58%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.9790 97.90%
P-glycoprotein inhibitior + 0.6482 64.82%
P-glycoprotein substrate - 0.9234 92.34%
CYP3A4 substrate - 0.5133 51.33%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7471 74.71%
CYP3A4 inhibition - 0.8810 88.10%
CYP2C9 inhibition - 0.5614 56.14%
CYP2C19 inhibition - 0.5173 51.73%
CYP2D6 inhibition - 0.9394 93.94%
CYP1A2 inhibition + 0.6060 60.60%
CYP2C8 inhibition - 0.9042 90.42%
CYP inhibitory promiscuity - 0.6901 69.01%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6928 69.28%
Carcinogenicity (trinary) Non-required 0.5325 53.25%
Eye corrosion - 0.8670 86.70%
Eye irritation - 0.8885 88.85%
Skin irritation + 0.6080 60.80%
Skin corrosion - 0.9665 96.65%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7007 70.07%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation + 0.8764 87.64%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.8444 84.44%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.6735 67.35%
Acute Oral Toxicity (c) III 0.7682 76.82%
Estrogen receptor binding + 0.6163 61.63%
Androgen receptor binding - 0.6601 66.01%
Thyroid receptor binding + 0.6751 67.51%
Glucocorticoid receptor binding + 0.6279 62.79%
Aromatase binding - 0.5180 51.80%
PPAR gamma + 0.6959 69.59%
Honey bee toxicity - 0.7035 70.35%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9275 92.75%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.89% 91.11%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.33% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.13% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 87.77% 85.14%
CHEMBL3401 O75469 Pregnane X receptor 86.09% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.29% 94.45%

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 693
LOTUS LTS0253305
wikiData Q105230172