[(2R,4R,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate

Details

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Internal ID 764dd39a-1f78-436c-8e17-77bb7298ca7c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name [(2R,4R,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate
SMILES (Canonical) CC1C(C(C(C(O1)OC2C(OC(C(C2O)O)OC3C(C(OC(C3OC(=O)C=CC4=CC=C(C=C4)O)CO)OCC=C(C)CCC=C(C)C)O)C)O)O)O
SMILES (Isomeric) C[C@H]1[C@@H]([C@H]([C@H]([C@@H](O1)O[C@H]2[C@@H](O[C@H]([C@@H]([C@@H]2O)O)O[C@@H]3[C@H]([C@@H](O[C@@H](C3OC(=O)/C=C/C4=CC=C(C=C4)O)CO)OC/C=C(\C)/CCC=C(C)C)O)C)O)O)O
InChI InChI=1S/C37H54O16/c1-18(2)7-6-8-19(3)15-16-47-35-31(46)34(33(24(17-38)50-35)51-25(40)14-11-22-9-12-23(39)13-10-22)53-37-30(45)28(43)32(21(5)49-37)52-36-29(44)27(42)26(41)20(4)48-36/h7,9-15,20-21,24,26-39,41-46H,6,8,16-17H2,1-5H3/b14-11+,19-15+/t20-,21-,24+,26-,27+,28-,29+,30+,31+,32-,33?,34+,35+,36-,37-/m0/s1
InChI Key WXMRZJXXQKPFTD-RGVGUNFNSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C37H54O16
Molecular Weight 754.80 g/mol
Exact Mass 754.34118563 g/mol
Topological Polar Surface Area (TPSA) 244.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.17
H-Bond Acceptor 16
H-Bond Donor 8
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2R,4R,5R,6R)-4-[(2S,3R,4S,5R,6S)-3,4-dihydroxy-6-methyl-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxy-6-[(2E)-3,7-dimethylocta-2,6-dienoxy]-5-hydroxy-2-(hydroxymethyl)oxan-3-yl] (E)-3-(4-hydroxyphenyl)prop-2-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5574 55.74%
Caco-2 - 0.8828 88.28%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.9000 90.00%
Subcellular localzation Mitochondria 0.8734 87.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8522 85.22%
OATP1B3 inhibitior + 0.8306 83.06%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8773 87.73%
P-glycoprotein inhibitior + 0.6358 63.58%
P-glycoprotein substrate - 0.5548 55.48%
CYP3A4 substrate + 0.6758 67.58%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8715 87.15%
CYP3A4 inhibition - 0.7232 72.32%
CYP2C9 inhibition - 0.8111 81.11%
CYP2C19 inhibition - 0.6721 67.21%
CYP2D6 inhibition - 0.8625 86.25%
CYP1A2 inhibition - 0.7000 70.00%
CYP2C8 inhibition + 0.6863 68.63%
CYP inhibitory promiscuity - 0.8219 82.19%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9400 94.00%
Carcinogenicity (trinary) Non-required 0.6829 68.29%
Eye corrosion - 0.9909 99.09%
Eye irritation - 0.9169 91.69%
Skin irritation - 0.7690 76.90%
Skin corrosion - 0.9607 96.07%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6843 68.43%
Micronuclear - 0.8400 84.00%
Hepatotoxicity - 0.8125 81.25%
skin sensitisation - 0.8274 82.74%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.8086 80.86%
Acute Oral Toxicity (c) III 0.6932 69.32%
Estrogen receptor binding + 0.7657 76.57%
Androgen receptor binding + 0.5421 54.21%
Thyroid receptor binding - 0.5132 51.32%
Glucocorticoid receptor binding + 0.6341 63.41%
Aromatase binding - 0.5000 50.00%
PPAR gamma + 0.7066 70.66%
Honey bee toxicity - 0.7018 70.18%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5355 53.55%
Fish aquatic toxicity + 0.9831 98.31%

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 99.14% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.77% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 94.75% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.40% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 92.19% 89.00%
CHEMBL3060 Q9Y345 Glycine transporter 2 92.04% 99.17%
CHEMBL2581 P07339 Cathepsin D 91.41% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 90.88% 96.00%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 89.41% 93.10%
CHEMBL3714130 P46095 G-protein coupled receptor 6 85.57% 97.36%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 82.26% 95.89%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 80.72% 85.00%

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.
Ligustrum robustum

Cross-Links

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PubChem 163188507
LOTUS LTS0021805
wikiData Q105314762