[(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-[[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxymethyl]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate

Details

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Internal ID c86ff6f0-2243-4f69-96b7-0537778d9d37
Taxonomy Lipids and lipid-like molecules > Saccharolipids
IUPAC Name [(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-[[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxymethyl]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)prop-2-enoate
SMILES (Canonical) C1=CC(=C(C=C1C=CC(=O)OC2C(C(C(OC2O)COC(=O)CC3(C=CC(=O)C=C3)O)O)O)O)O
SMILES (Isomeric) C1=CC(=C(C=C1/C=C/C(=O)O[C@@H]2[C@H]([C@@H]([C@H](O[C@H]2O)COC(=O)CC3(C=CC(=O)C=C3)O)O)O)O)O
InChI InChI=1S/C23H24O12/c24-13-5-7-23(32,8-6-13)10-18(28)33-11-16-19(29)20(30)21(22(31)34-16)35-17(27)4-2-12-1-3-14(25)15(26)9-12/h1-9,16,19-22,25-26,29-32H,10-11H2/b4-2+/t16-,19-,20+,21-,22-/m1/s1
InChI Key ZFGSMBPBMKZCPY-XDTWIQQOSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C23H24O12
Molecular Weight 492.40 g/mol
Exact Mass 492.12677620 g/mol
Topological Polar Surface Area (TPSA) 200.00 Ų
XlogP -0.50
Atomic LogP (AlogP) -1.18
H-Bond Acceptor 12
H-Bond Donor 6
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of [(2R,3R,4S,5S,6R)-2,4,5-trihydroxy-6-[[2-(1-hydroxy-4-oxocyclohexa-2,5-dien-1-yl)acetyl]oxymethyl]oxan-3-yl] (E)-3-(3,4-dihydroxyphenyl)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 - 0.5398 53.98%
Caco-2 - 0.8902 89.02%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7857 78.57%
Subcellular localzation Mitochondria 0.6435 64.35%
OATP2B1 inhibitior - 0.8473 84.73%
OATP1B1 inhibitior + 0.8796 87.96%
OATP1B3 inhibitior + 0.9238 92.38%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6837 68.37%
P-glycoprotein inhibitior - 0.5200 52.00%
P-glycoprotein substrate - 0.7659 76.59%
CYP3A4 substrate + 0.6461 64.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8611 86.11%
CYP3A4 inhibition - 0.7991 79.91%
CYP2C9 inhibition - 0.8393 83.93%
CYP2C19 inhibition - 0.8352 83.52%
CYP2D6 inhibition - 0.9101 91.01%
CYP1A2 inhibition - 0.9106 91.06%
CYP2C8 inhibition + 0.6247 62.47%
CYP inhibitory promiscuity - 0.9073 90.73%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6621 66.21%
Eye corrosion - 0.9911 99.11%
Eye irritation - 0.9005 90.05%
Skin irritation - 0.7968 79.68%
Skin corrosion - 0.9383 93.83%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4748 47.48%
Micronuclear + 0.5692 56.92%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation - 0.7436 74.36%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7333 73.33%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.9536 95.36%
Acute Oral Toxicity (c) III 0.7086 70.86%
Estrogen receptor binding + 0.5928 59.28%
Androgen receptor binding + 0.5673 56.73%
Thyroid receptor binding - 0.5280 52.80%
Glucocorticoid receptor binding + 0.5716 57.16%
Aromatase binding + 0.5458 54.58%
PPAR gamma + 0.5519 55.19%
Honey bee toxicity - 0.7628 76.28%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9460 94.60%

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 99.85% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 99.47% 91.49%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.12% 89.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 95.29% 86.33%
CHEMBL226 P30542 Adenosine A1 receptor 95.13% 95.93%
CHEMBL221 P23219 Cyclooxygenase-1 92.28% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 91.58% 96.00%
CHEMBL3194 P02766 Transthyretin 91.19% 90.71%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.03% 95.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.76% 94.45%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.62% 97.09%
CHEMBL1860 P10827 Thyroid hormone receptor alpha 86.60% 99.15%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 86.44% 94.80%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.21% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 85.69% 94.73%
CHEMBL3788 O00444 Serine/threonine-protein kinase PLK4 84.90% 83.65%
CHEMBL4208 P20618 Proteasome component C5 82.70% 90.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 81.91% 97.28%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 80.68% 91.07%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.14% 99.17%

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.
Senecio scandens

Cross-Links

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PubChem 163191410
LOTUS LTS0257511
wikiData Q105374146