(1S,4aR,7S,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid

Details

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Internal ID 6c44ca7f-575e-4420-bb05-3b0e2e29be0e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Iridoid O-glycosides
IUPAC Name (1S,4aR,7S,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid
SMILES (Canonical) COC1=C(C=CC(=C1)C=CC(=O)OCC2C(C(C(C(O2)OC3C4C(C=CC4(CO)O)C(=CO3)C(=O)O)O)O)O)O
SMILES (Isomeric) COC1=C(C=CC(=C1)/C=C/C(=O)OC[C@@H]2[C@H]([C@@H]([C@H]([C@@H](O2)O[C@H]3[C@H]4[C@@H](C=C[C@]4(CO)O)C(=CO3)C(=O)O)O)O)O)O
InChI InChI=1S/C26H30O14/c1-36-16-8-12(2-4-15(16)28)3-5-18(29)37-10-17-20(30)21(31)22(32)25(39-17)40-24-19-13(6-7-26(19,35)11-27)14(9-38-24)23(33)34/h2-9,13,17,19-22,24-25,27-28,30-32,35H,10-11H2,1H3,(H,33,34)/b5-3+/t13-,17+,19+,20+,21-,22+,24-,25-,26+/m0/s1
InChI Key KAKMKHUXDFAONC-NUULAFJDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C26H30O14
Molecular Weight 566.50 g/mol
Exact Mass 566.16355563 g/mol
Topological Polar Surface Area (TPSA) 222.00 Ų
XlogP -1.40
Atomic LogP (AlogP) -1.37
H-Bond Acceptor 13
H-Bond Donor 7
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1S,4aR,7S,7aS)-7-hydroxy-7-(hydroxymethyl)-1-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-[[(E)-3-(4-hydroxy-3-methoxyphenyl)prop-2-enoyl]oxymethyl]oxan-2-yl]oxy-4a,7a-dihydro-1H-cyclopenta[c]pyran-4-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7045 70.45%
Caco-2 - 0.9067 90.67%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.5158 51.58%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.8125 81.25%
OATP1B3 inhibitior + 0.9677 96.77%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7001 70.01%
P-glycoprotein inhibitior - 0.5060 50.60%
P-glycoprotein substrate - 0.5840 58.40%
CYP3A4 substrate + 0.6712 67.12%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8682 86.82%
CYP3A4 inhibition - 0.9094 90.94%
CYP2C9 inhibition - 0.7978 79.78%
CYP2C19 inhibition - 0.7305 73.05%
CYP2D6 inhibition - 0.8718 87.18%
CYP1A2 inhibition - 0.8196 81.96%
CYP2C8 inhibition + 0.7503 75.03%
CYP inhibitory promiscuity - 0.8182 81.82%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.5999 59.99%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9301 93.01%
Skin irritation - 0.7755 77.55%
Skin corrosion - 0.9403 94.03%
Ames mutagenesis - 0.6323 63.23%
Human Ether-a-go-go-Related Gene inhibition + 0.6462 64.62%
Micronuclear + 0.5433 54.33%
Hepatotoxicity - 0.7412 74.12%
skin sensitisation - 0.7969 79.69%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity - 0.8862 88.62%
Acute Oral Toxicity (c) III 0.5158 51.58%
Estrogen receptor binding + 0.7680 76.80%
Androgen receptor binding + 0.6088 60.88%
Thyroid receptor binding + 0.5236 52.36%
Glucocorticoid receptor binding + 0.6462 64.62%
Aromatase binding + 0.5493 54.93%
PPAR gamma + 0.6665 66.65%
Honey bee toxicity - 0.7899 78.99%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.7531 75.31%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 98.88% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.72% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.50% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 96.90% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 96.36% 96.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.78% 95.56%
CHEMBL3194 P02766 Transthyretin 93.03% 90.71%
CHEMBL4208 P20618 Proteasome component C5 90.50% 90.00%
CHEMBL1951 P21397 Monoamine oxidase A 90.17% 91.49%
CHEMBL225 P28335 Serotonin 2c (5-HT2c) receptor 88.86% 89.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.80% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.47% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.76% 94.45%
CHEMBL5028 O14672 ADAM10 80.71% 97.50%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.69% 96.90%

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.
Paederia foetida

Cross-Links

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PubChem 154496052
LOTUS LTS0249603
wikiData Q105137880