2-Propenoic acid, 3-(3-hydroxy-4-methoxyphenyl)-, (3beta,19epsilon)-lup-20(29)-en-3-yl ester, (2E)-

Details

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Internal ID aa0f4df4-27e2-4802-9fa6-0779867ccdaa
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name [(3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] (E)-3-(3-hydroxy-4-methoxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C40H58O4/c1-25(2)27-16-19-37(5)22-23-39(7)28(35(27)37)12-14-32-38(6)20-18-33(36(3,4)31(38)17-21-40(32,39)8)44-34(42)15-11-26-10-13-30(43-9)29(41)24-26/h10-11,13,15,24,27-28,31-33,35,41H,1,12,14,16-23H2,2-9H3/b15-11+/t27?,28-,31+,32-,33+,35-,37-,38+,39-,40-/m1/s1
InChI Key FKPQGZKVKUXBGD-HSHPSVAASA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C40H58O4
Molecular Weight 602.90 g/mol
Exact Mass 602.43351033 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 12.10
Atomic LogP (AlogP) 10.00
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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2-Propenoic acid, 3-(3-hydroxy-4-methoxyphenyl)-, (3.beta.,19.epsilon.)-lup-20(29)-en-3-yl ester, (2E)-

2D Structure

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2D Structure of 2-Propenoic acid, 3-(3-hydroxy-4-methoxyphenyl)-, (3beta,19epsilon)-lup-20(29)-en-3-yl ester, (2E)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9956 99.56%
Caco-2 - 0.8152 81.52%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8038 80.38%
OATP2B1 inhibitior - 0.7121 71.21%
OATP1B1 inhibitior + 0.8708 87.08%
OATP1B3 inhibitior + 0.8062 80.62%
MATE1 inhibitior - 0.7200 72.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9717 97.17%
P-glycoprotein inhibitior + 0.7789 77.89%
P-glycoprotein substrate - 0.5127 51.27%
CYP3A4 substrate + 0.7229 72.29%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8548 85.48%
CYP3A4 inhibition + 0.5229 52.29%
CYP2C9 inhibition - 0.6446 64.46%
CYP2C19 inhibition + 0.5574 55.74%
CYP2D6 inhibition - 0.9090 90.90%
CYP1A2 inhibition + 0.6022 60.22%
CYP2C8 inhibition + 0.8509 85.09%
CYP inhibitory promiscuity - 0.8417 84.17%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8820 88.20%
Carcinogenicity (trinary) Non-required 0.6260 62.60%
Eye corrosion - 0.9940 99.40%
Eye irritation - 0.9261 92.61%
Skin irritation - 0.6061 60.61%
Skin corrosion - 0.9666 96.66%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8163 81.63%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.7231 72.31%
skin sensitisation - 0.8001 80.01%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.8111 81.11%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.8888 88.88%
Acute Oral Toxicity (c) IV 0.4556 45.56%
Estrogen receptor binding + 0.7686 76.86%
Androgen receptor binding + 0.8080 80.80%
Thyroid receptor binding + 0.5554 55.54%
Glucocorticoid receptor binding + 0.7824 78.24%
Aromatase binding + 0.7632 76.32%
PPAR gamma + 0.7320 73.20%
Honey bee toxicity - 0.6768 67.68%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5200 52.00%
Fish aquatic toxicity + 1.0000 100.00%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 97.71% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.57% 91.11%
CHEMBL241 Q14432 Phosphodiesterase 3A 97.35% 92.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.26% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 96.15% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.40% 95.56%
CHEMBL3788 O00444 Serine/threonine-protein kinase PLK4 91.91% 83.65%
CHEMBL1937 Q92769 Histone deacetylase 2 91.57% 94.75%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.73% 95.89%
CHEMBL1951 P21397 Monoamine oxidase A 88.44% 91.49%
CHEMBL2581 P07339 Cathepsin D 87.28% 98.95%
CHEMBL3194 P02766 Transthyretin 86.95% 90.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.52% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.21% 89.00%
CHEMBL340 P08684 Cytochrome P450 3A4 85.49% 91.19%
CHEMBL3713062 P10646 Tissue factor pathway inhibitor 85.40% 97.33%
CHEMBL2535 P11166 Glucose transporter 84.20% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.06% 97.09%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 83.81% 96.09%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.56% 95.50%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 83.49% 89.62%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 83.33% 91.03%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 82.08% 85.30%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.01% 100.00%
CHEMBL2146302 O94925 Glutaminase kidney isoform, mitochondrial 81.05% 100.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.78% 91.07%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.72% 96.95%
CHEMBL3192 Q9BY41 Histone deacetylase 8 80.70% 93.99%

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.
Euclea natalensis

Cross-Links

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PubChem 162801021
LOTUS LTS0231186
wikiData Q104996731