Myriceron caffeoyl ester

Details

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Internal ID 747e940e-05c6-4e58-916a-1e1da61a02b5
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (4aS,6aR,6aR,6bR,8aR,12aR,14bS)-6a-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-2,2,6b,9,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C39H52O7/c1-34(2)17-18-38(33(44)45)19-20-39(23-46-32(43)12-8-24-7-10-27(40)28(41)21-24)25(26(38)22-34)9-11-30-36(5)15-14-31(42)35(3,4)29(36)13-16-37(30,39)6/h7-10,12,21,26,29-30,40-41H,11,13-20,22-23H2,1-6H3,(H,44,45)/b12-8+/t26-,29-,30+,36-,37+,38-,39-/m0/s1
InChI Key RHAKBYCTYSBWIE-QWZNMBRFSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C39H52O7
Molecular Weight 632.80 g/mol
Exact Mass 632.37130399 g/mol
Topological Polar Surface Area (TPSA) 121.00 Ų
XlogP 7.70
Atomic LogP (AlogP) 8.09
H-Bond Acceptor 6
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

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142877-49-4
(4aS,6aR,6aR,6bR,8aR,12aR,14bS)-6a-[[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxymethyl]-2,2,6b,9,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylic acid
(4aS,6aR,6aR,6bR,8aR,12aR,14bS)-6a-(((E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl)oxymethyl)-2,2,6b,9,9,12a-hexamethyl-10-oxo-3,4,5,6,6a,7,8,8a,11,12,13,14b-dodecahydro-1H-picene-4a-carboxylic acid
RefChem:160383
CHEMBL3601500
27((3-(3,4-Dihydroxyphenyl)-1-oxo-2-propenyl)oxy)-3-oxoolean-12-en-28-oic acid
Olean-12-en-28-oic acid, 27((3-(3,4-dihydroxyphenyl)-1-oxo-2-propenyl)oxy)-3-oxo-
BDBM50108104

2D Structure

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2D Structure of Myriceron caffeoyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9883 98.83%
Caco-2 - 0.7905 79.05%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.9353 93.53%
OATP2B1 inhibitior - 0.7100 71.00%
OATP1B1 inhibitior + 0.8266 82.66%
OATP1B3 inhibitior - 0.3777 37.77%
MATE1 inhibitior - 0.7000 70.00%
OCT2 inhibitior - 0.7276 72.76%
BSEP inhibitior + 0.9955 99.55%
P-glycoprotein inhibitior + 0.8017 80.17%
P-glycoprotein substrate - 0.5682 56.82%
CYP3A4 substrate + 0.6833 68.33%
CYP2C9 substrate - 0.8032 80.32%
CYP2D6 substrate - 0.8868 88.68%
CYP3A4 inhibition - 0.7544 75.44%
CYP2C9 inhibition - 0.6317 63.17%
CYP2C19 inhibition - 0.6658 66.58%
CYP2D6 inhibition - 0.9040 90.40%
CYP1A2 inhibition + 0.7106 71.06%
CYP2C8 inhibition + 0.7966 79.66%
CYP inhibitory promiscuity - 0.7955 79.55%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.6779 67.79%
Eye corrosion - 0.9937 99.37%
Eye irritation - 0.9214 92.14%
Skin irritation - 0.6800 68.00%
Skin corrosion - 0.9612 96.12%
Ames mutagenesis - 0.7254 72.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6516 65.16%
Micronuclear - 0.7500 75.00%
Hepatotoxicity - 0.7084 70.84%
skin sensitisation - 0.8361 83.61%
Respiratory toxicity + 0.7778 77.78%
Reproductive toxicity + 0.9444 94.44%
Mitochondrial toxicity + 0.5500 55.00%
Nephrotoxicity - 0.9138 91.38%
Acute Oral Toxicity (c) III 0.5548 55.48%
Estrogen receptor binding + 0.7810 78.10%
Androgen receptor binding + 0.7857 78.57%
Thyroid receptor binding + 0.6052 60.52%
Glucocorticoid receptor binding + 0.8414 84.14%
Aromatase binding + 0.7189 71.89%
PPAR gamma + 0.7310 73.10%
Honey bee toxicity - 0.7601 76.01%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5700 57.00%
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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.57% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 97.13% 86.33%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 96.93% 95.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.32% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.43% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.29% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.52% 96.09%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 89.56% 91.71%
CHEMBL2581 P07339 Cathepsin D 88.34% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 88.17% 90.17%
CHEMBL1937 Q92769 Histone deacetylase 2 87.97% 94.75%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.22% 99.15%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.23% 90.71%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.94% 89.00%
CHEMBL4208 P20618 Proteasome component C5 81.94% 90.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.88% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.58% 100.00%
CHEMBL1914 P06276 Butyrylcholinesterase 80.94% 95.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.43% 99.23%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 80.17% 96.00%

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.
Bixa orellana
Hibiscus taiwanensis

Cross-Links

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PubChem 6450144
LOTUS LTS0228042
wikiData Q105151002