[1-[3-[2-[3-(3-Acetyloxy-4-hydroxy-4,8-dimethylnon-7-enyl)-3-methyloxiran-2-yl]ethyl]-2-methyloxiran-2-yl]-4-hydroxy-4,8-dimethylnon-7-en-3-yl] acetate

Details

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Internal ID d8352500-04c2-4698-b33d-2c525825a5ad
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name [1-[3-[2-[3-(3-acetyloxy-4-hydroxy-4,8-dimethylnon-7-enyl)-3-methyloxiran-2-yl]ethyl]-2-methyloxiran-2-yl]-4-hydroxy-4,8-dimethylnon-7-en-3-yl] acetate
SMILES (Canonical) CC(=CCCC(C)(C(CCC1(C(O1)CCC2C(O2)(C)CCC(C(C)(CCC=C(C)C)O)OC(=O)C)C)OC(=O)C)O)C
SMILES (Isomeric) CC(=CCCC(C)(C(CCC1(C(O1)CCC2C(O2)(C)CCC(C(C)(CCC=C(C)C)O)OC(=O)C)C)OC(=O)C)O)C
InChI InChI=1S/C34H58O8/c1-23(2)13-11-19-31(7,37)27(39-25(5)35)17-21-33(9)29(41-33)15-16-30-34(10,42-30)22-18-28(40-26(6)36)32(8,38)20-12-14-24(3)4/h13-14,27-30,37-38H,11-12,15-22H2,1-10H3
InChI Key OXMCWUYGHSNTPP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C34H58O8
Molecular Weight 594.80 g/mol
Exact Mass 594.41316880 g/mol
Topological Polar Surface Area (TPSA) 118.00 Ų
XlogP 5.90
Atomic LogP (AlogP) 6.50
H-Bond Acceptor 8
H-Bond Donor 2
Rotatable Bonds 19

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [1-[3-[2-[3-(3-Acetyloxy-4-hydroxy-4,8-dimethylnon-7-enyl)-3-methyloxiran-2-yl]ethyl]-2-methyloxiran-2-yl]-4-hydroxy-4,8-dimethylnon-7-en-3-yl] acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9122 91.22%
Caco-2 - 0.7850 78.50%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6671 66.71%
OATP2B1 inhibitior - 0.7156 71.56%
OATP1B1 inhibitior + 0.9207 92.07%
OATP1B3 inhibitior + 0.8987 89.87%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior + 0.9680 96.80%
P-glycoprotein inhibitior + 0.7672 76.72%
P-glycoprotein substrate - 0.7706 77.06%
CYP3A4 substrate + 0.6200 62.00%
CYP2C9 substrate - 0.7958 79.58%
CYP2D6 substrate - 0.8730 87.30%
CYP3A4 inhibition - 0.5923 59.23%
CYP2C9 inhibition - 0.6892 68.92%
CYP2C19 inhibition - 0.7193 71.93%
CYP2D6 inhibition - 0.9236 92.36%
CYP1A2 inhibition - 0.7554 75.54%
CYP2C8 inhibition - 0.7610 76.10%
CYP inhibitory promiscuity - 0.9070 90.70%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8243 82.43%
Carcinogenicity (trinary) Non-required 0.6667 66.67%
Eye corrosion - 0.9771 97.71%
Eye irritation - 0.9029 90.29%
Skin irritation - 0.6155 61.55%
Skin corrosion - 0.9596 95.96%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6576 65.76%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.5257 52.57%
skin sensitisation - 0.6318 63.18%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5145 51.45%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity + 0.6687 66.87%
Acute Oral Toxicity (c) III 0.5549 55.49%
Estrogen receptor binding + 0.7423 74.23%
Androgen receptor binding + 0.5278 52.78%
Thyroid receptor binding + 0.5754 57.54%
Glucocorticoid receptor binding + 0.6642 66.42%
Aromatase binding + 0.7094 70.94%
PPAR gamma + 0.6851 68.51%
Honey bee toxicity - 0.7235 72.35%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9762 97.62%

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 96.32% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.08% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.79% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.01% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.81% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 89.73% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 88.51% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.98% 99.17%
CHEMBL340 P08684 Cytochrome P450 3A4 87.44% 91.19%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 86.92% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 85.70% 97.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.18% 85.14%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.91% 96.77%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.26% 94.33%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.40% 86.33%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.16% 97.28%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 81.02% 96.47%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.76% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.69% 96.95%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.64% 97.14%

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 73837140
LOTUS LTS0217282
wikiData Q105202780