9Beta-O-(E-P-Hydroxycinnamoyl)-1Beta,6Beta-Dihydroxy-Trans-Eudesm-3-En-6-O-Beta-D-Glucopyranoside

Details

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Internal ID d1fa3574-34de-4bb0-95fc-3f90aa9edc54
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name [(1S,3S,4R,4aS,8R,8aR)-8-hydroxy-5,8a-dimethyl-3-propan-2-yl-4-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,4,4a,7,8-hexahydro-1H-naphthalen-1-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C30H42O10/c1-15(2)19-13-22(39-23(34)12-8-17-6-9-18(32)10-7-17)30(4)21(33)11-5-16(3)24(30)28(19)40-29-27(37)26(36)25(35)20(14-31)38-29/h5-10,12,15,19-22,24-29,31-33,35-37H,11,13-14H2,1-4H3/b12-8+/t19-,20+,21+,22-,24+,25+,26-,27+,28+,29-,30+/m0/s1
InChI Key FYIRTYWAWSCPCM-RQDXIEOQSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C30H42O10
Molecular Weight 562.60 g/mol
Exact Mass 562.27779753 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP 2.30
Atomic LogP (AlogP) 1.51
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 7

Synonyms

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((1S,3S,4R,4aS,8R,8aR)-8-hydroxy-5,8a-dimethyl-3-propan-2-yl-4-((2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl)oxy-2,3,4,4a,7,8-hexahydro-1H-naphthalen-1-yl) (E)-3-(4-hydroxyphenyl)prop-2-enoate
9Beta-O-(E-P-Hydroxycinnamoyl)-1Beta,6Beta-Dihydroxy-Trans-Eudesm-3-En-6-O-Beta-D-Glucopyranoside
CHEMBL2011643
BDBM50379291

2D Structure

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2D Structure of 9Beta-O-(E-P-Hydroxycinnamoyl)-1Beta,6Beta-Dihydroxy-Trans-Eudesm-3-En-6-O-Beta-D-Glucopyranoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9154 91.54%
Caco-2 - 0.8554 85.54%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.8857 88.57%
Subcellular localzation Mitochondria 0.7255 72.55%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8568 85.68%
OATP1B3 inhibitior + 0.8880 88.80%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior + 0.7464 74.64%
P-glycoprotein inhibitior - 0.5096 50.96%
P-glycoprotein substrate - 0.5544 55.44%
CYP3A4 substrate + 0.6985 69.85%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8760 87.60%
CYP3A4 inhibition - 0.9517 95.17%
CYP2C9 inhibition - 0.8174 81.74%
CYP2C19 inhibition - 0.7196 71.96%
CYP2D6 inhibition - 0.8409 84.09%
CYP1A2 inhibition + 0.5134 51.34%
CYP2C8 inhibition + 0.7032 70.32%
CYP inhibitory promiscuity - 0.8082 80.82%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7149 71.49%
Eye corrosion - 0.9916 99.16%
Eye irritation - 0.9423 94.23%
Skin irritation - 0.7376 73.76%
Skin corrosion - 0.9483 94.83%
Ames mutagenesis - 0.6337 63.37%
Human Ether-a-go-go-Related Gene inhibition + 0.6510 65.10%
Micronuclear - 0.6826 68.26%
Hepatotoxicity - 0.7439 74.39%
skin sensitisation - 0.8117 81.17%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8674 86.74%
Acute Oral Toxicity (c) III 0.5269 52.69%
Estrogen receptor binding + 0.8046 80.46%
Androgen receptor binding + 0.7034 70.34%
Thyroid receptor binding + 0.5479 54.79%
Glucocorticoid receptor binding + 0.6504 65.04%
Aromatase binding + 0.6130 61.30%
PPAR gamma + 0.7272 72.72%
Honey bee toxicity - 0.6992 69.92%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9616 96.16%

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 99.03% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.69% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.09% 97.09%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 93.89% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.76% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.63% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.90% 89.00%
CHEMBL2581 P07339 Cathepsin D 92.10% 98.95%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 90.35% 89.67%
CHEMBL206 P03372 Estrogen receptor alpha 90.05% 97.64%
CHEMBL3401 O75469 Pregnane X receptor 89.68% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.10% 99.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.99% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.62% 94.45%
CHEMBL1937 Q92769 Histone deacetylase 2 87.37% 94.75%
CHEMBL4208 P20618 Proteasome component C5 87.00% 90.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.01% 95.50%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.18% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.18% 95.89%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 84.97% 85.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 82.63% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.42% 96.95%
CHEMBL226 P30542 Adenosine A1 receptor 82.23% 95.93%

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.
Miyamayomena koraiensis

Cross-Links

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PubChem 57333878
NPASS NPC204644
LOTUS LTS0008614
wikiData Q105004513