Hymenoside K

Details

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Internal ID 2901b920-b111-4c42-aad3-7b109439ccd1
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acyl glycosides > Fatty acyl glycosides of mono- and disaccharides
IUPAC Name [(2R,3R,4S,5S,6R)-4,5-dihydroxy-6-(hydroxymethyl)-2-[(E)-4-hydroxy-2-methylbut-2-enoxy]oxan-3-yl] 2-(3,4-dihydroxyphenyl)acetate
SMILES (Canonical) CC(=CCO)COC1C(C(C(C(O1)CO)O)O)OC(=O)CC2=CC(=C(C=C2)O)O
SMILES (Isomeric) C/C(=C\CO)/CO[C@H]1[C@@H]([C@H]([C@@H]([C@H](O1)CO)O)O)OC(=O)CC2=CC(=C(C=C2)O)O
InChI InChI=1S/C19H26O10/c1-10(4-5-20)9-27-19-18(17(26)16(25)14(8-21)28-19)29-15(24)7-11-2-3-12(22)13(23)6-11/h2-4,6,14,16-23,25-26H,5,7-9H2,1H3/b10-4+/t14-,16-,17+,18-,19-/m1/s1
InChI Key TXJUGISOVAMAEN-DWKLNFMMSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C19H26O10
Molecular Weight 414.40 g/mol
Exact Mass 414.15259702 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP -0.30
Atomic LogP (AlogP) -1.05
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hymenoside K

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.6501 65.01%
Caco-2 - 0.8263 82.63%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.7677 76.77%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.8447 84.47%
OATP1B3 inhibitior + 0.9494 94.94%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6485 64.85%
P-glycoprotein inhibitior - 0.6813 68.13%
P-glycoprotein substrate - 0.8316 83.16%
CYP3A4 substrate + 0.5842 58.42%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8683 86.83%
CYP3A4 inhibition - 0.9144 91.44%
CYP2C9 inhibition - 0.7969 79.69%
CYP2C19 inhibition - 0.6559 65.59%
CYP2D6 inhibition - 0.8228 82.28%
CYP1A2 inhibition - 0.6413 64.13%
CYP2C8 inhibition + 0.4907 49.07%
CYP inhibitory promiscuity - 0.5322 53.22%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.7154 71.54%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.9274 92.74%
Skin irritation - 0.8013 80.13%
Skin corrosion - 0.9533 95.33%
Ames mutagenesis - 0.6670 66.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5944 59.44%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation - 0.7735 77.35%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity - 0.7872 78.72%
Acute Oral Toxicity (c) III 0.6244 62.44%
Estrogen receptor binding + 0.7469 74.69%
Androgen receptor binding + 0.6117 61.17%
Thyroid receptor binding - 0.5261 52.61%
Glucocorticoid receptor binding - 0.5066 50.66%
Aromatase binding + 0.5663 56.63%
PPAR gamma + 0.5790 57.90%
Honey bee toxicity - 0.8077 80.77%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7655 76.55%
Fish aquatic toxicity + 0.9811 98.11%

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 99.33% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.16% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.89% 94.45%
CHEMBL1951 P21397 Monoamine oxidase A 93.72% 91.49%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.14% 99.17%
CHEMBL2581 P07339 Cathepsin D 93.05% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 91.51% 94.73%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.54% 86.92%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.58% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.57% 89.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.88% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 83.68% 96.00%
CHEMBL3194 P02766 Transthyretin 82.50% 90.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.32% 96.95%
CHEMBL340 P08684 Cytochrome P450 3A4 81.50% 91.19%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.24% 86.33%

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.
Hymenophyllum barbatum

Cross-Links

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PubChem 10982563
LOTUS LTS0245555
wikiData Q105266792