Gymnoside

Details

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Internal ID 5de0ddfb-c7ab-4124-a715-f20ba7a7a3bb
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > Phenolic glycosides
IUPAC Name (3R)-3-hydroxy-5-methyl-3-[[4-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxyphenyl]methoxycarbonyl]hexanoic acid
SMILES (Canonical) CC(C)CC(CC(=O)O)(C(=O)OCC1=CC=C(C=C1)OC2C(C(C(C(O2)CO)O)O)O)O
SMILES (Isomeric) CC(C)C[C@@](CC(=O)O)(C(=O)OCC1=CC=C(C=C1)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O)O
InChI InChI=1S/C21H30O11/c1-11(2)7-21(29,8-15(23)24)20(28)30-10-12-3-5-13(6-4-12)31-19-18(27)17(26)16(25)14(9-22)32-19/h3-6,11,14,16-19,22,25-27,29H,7-10H2,1-2H3,(H,23,24)/t14-,16-,17+,18-,19-,21-/m1/s1
InChI Key PYJUFJBNDQMBDO-XSEUIGDCSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C21H30O11
Molecular Weight 458.50 g/mol
Exact Mass 458.17881177 g/mol
Topological Polar Surface Area (TPSA) 183.00 Ų
XlogP 0.20
Atomic LogP (AlogP) -0.84
H-Bond Acceptor 10
H-Bond Donor 6
Rotatable Bonds 10

Synonyms

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CHEMBL4870737

2D Structure

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2D Structure of Gymnoside

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.6200 62.00%
Caco-2 - 0.8457 84.57%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.7923 79.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8962 89.62%
OATP1B3 inhibitior + 0.9172 91.72%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.7648 76.48%
P-glycoprotein inhibitior - 0.6897 68.97%
P-glycoprotein substrate - 0.8488 84.88%
CYP3A4 substrate + 0.5876 58.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8877 88.77%
CYP3A4 inhibition - 0.8416 84.16%
CYP2C9 inhibition - 0.8039 80.39%
CYP2C19 inhibition - 0.8915 89.15%
CYP2D6 inhibition - 0.9423 94.23%
CYP1A2 inhibition - 0.8260 82.60%
CYP2C8 inhibition - 0.6650 66.50%
CYP inhibitory promiscuity - 0.9503 95.03%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.6710 67.10%
Eye corrosion - 0.9928 99.28%
Eye irritation - 0.9394 93.94%
Skin irritation - 0.8445 84.45%
Skin corrosion - 0.9569 95.69%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6575 65.75%
Micronuclear - 0.7100 71.00%
Hepatotoxicity - 0.6375 63.75%
skin sensitisation - 0.8605 86.05%
Respiratory toxicity - 0.5333 53.33%
Reproductive toxicity + 0.6111 61.11%
Mitochondrial toxicity - 0.5250 52.50%
Nephrotoxicity - 0.8406 84.06%
Acute Oral Toxicity (c) III 0.6959 69.59%
Estrogen receptor binding + 0.5715 57.15%
Androgen receptor binding + 0.6084 60.84%
Thyroid receptor binding - 0.5268 52.68%
Glucocorticoid receptor binding + 0.6572 65.72%
Aromatase binding - 0.4889 48.89%
PPAR gamma - 0.6075 60.75%
Honey bee toxicity - 0.8143 81.43%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.7359 73.59%
Fish aquatic toxicity + 0.8908 89.08%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.07% 96.09%
CHEMBL2581 P07339 Cathepsin D 97.95% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 96.19% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.10% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 88.16% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.69% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.89% 95.89%
CHEMBL221 P23219 Cyclooxygenase-1 86.47% 90.17%
CHEMBL211 P08172 Muscarinic acetylcholine receptor M2 85.95% 94.97%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 85.79% 95.89%
CHEMBL220 P22303 Acetylcholinesterase 85.40% 94.45%
CHEMBL3437 Q16853 Amine oxidase, copper containing 84.78% 94.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.37% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 84.15% 96.00%
CHEMBL2179 P04062 Beta-glucocerebrosidase 84.04% 85.31%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 83.75% 94.62%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.88% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.87% 95.50%
CHEMBL4208 P20618 Proteasome component C5 81.55% 90.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.39% 94.00%

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.
Bletilla striata
Gymnadenia conopsea
Syzygium aromaticum

Cross-Links

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PubChem 11641120
NPASS NPC169761
LOTUS LTS0253635
wikiData Q105216626