Cistanoside G

Details

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Internal ID a3c204e0-198c-4684-8714-105f3320a460
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Glycosyl compounds > O-glycosyl compounds
IUPAC Name (2S,3R,4S,5S,6R)-2-[(2R,3R,4R,5R,6S)-3,5-dihydroxy-2-[2-(4-hydroxyphenyl)ethoxy]-6-methyloxan-4-yl]oxy-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical) CC1C(C(C(C(O1)OCCC2=CC=C(C=C2)O)O)OC3C(C(C(C(O3)CO)O)O)O)O
SMILES (Isomeric) C[C@H]1[C@H]([C@H]([C@H]([C@@H](O1)OCCC2=CC=C(C=C2)O)O)O[C@H]3[C@@H]([C@H]([C@@H]([C@H](O3)CO)O)O)O)O
InChI InChI=1S/C20H30O11/c1-9-13(23)18(31-20-16(26)15(25)14(24)12(8-21)30-20)17(27)19(29-9)28-7-6-10-2-4-11(22)5-3-10/h2-5,9,12-27H,6-8H2,1H3/t9-,12+,13+,14+,15-,16+,17+,18+,19+,20-/m0/s1
InChI Key PUNXDBIVFUQAAC-FYQUPJIJSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H30O11
Molecular Weight 446.40 g/mol
Exact Mass 446.17881177 g/mol
Topological Polar Surface Area (TPSA) 179.00 Ų
XlogP -1.50
Atomic LogP (AlogP) -2.40
H-Bond Acceptor 11
H-Bond Donor 7
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cistanoside G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.9023 90.23%
Caco-2 - 0.8591 85.91%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.7985 79.85%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8579 85.79%
OATP1B3 inhibitior + 0.9560 95.60%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8551 85.51%
P-glycoprotein inhibitior - 0.8435 84.35%
P-glycoprotein substrate - 0.7410 74.10%
CYP3A4 substrate + 0.5661 56.61%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8034 80.34%
CYP3A4 inhibition - 0.9558 95.58%
CYP2C9 inhibition - 0.8096 80.96%
CYP2C19 inhibition - 0.8920 89.20%
CYP2D6 inhibition - 0.9342 93.42%
CYP1A2 inhibition - 0.9142 91.42%
CYP2C8 inhibition + 0.5557 55.57%
CYP inhibitory promiscuity - 0.7800 78.00%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5835 58.35%
Eye corrosion - 0.9912 99.12%
Eye irritation - 0.9514 95.14%
Skin irritation - 0.8334 83.34%
Skin corrosion - 0.9619 96.19%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3788 37.88%
Micronuclear - 0.7641 76.41%
Hepatotoxicity - 0.9125 91.25%
skin sensitisation - 0.9024 90.24%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.6000 60.00%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity - 0.8243 82.43%
Acute Oral Toxicity (c) III 0.7036 70.36%
Estrogen receptor binding + 0.6061 60.61%
Androgen receptor binding - 0.5484 54.84%
Thyroid receptor binding + 0.6457 64.57%
Glucocorticoid receptor binding - 0.5759 57.59%
Aromatase binding + 0.5619 56.19%
PPAR gamma + 0.7211 72.11%
Honey bee toxicity - 0.7154 71.54%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5650 56.50%
Fish aquatic toxicity - 0.7249 72.49%

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 97.14% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.16% 96.09%
CHEMBL2581 P07339 Cathepsin D 93.68% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.49% 86.33%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.92% 94.62%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.28% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 88.47% 94.73%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 88.08% 86.92%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.63% 94.00%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.26% 95.89%
CHEMBL5608 Q16288 NT-3 growth factor receptor 83.51% 95.89%
CHEMBL5852 Q96P65 Pyroglutamylated RFamide peptide receptor 82.35% 85.00%
CHEMBL1944 P08473 Neprilysin 80.55% 92.63%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.39% 89.00%

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.
Cistanche deserticola
Cistanche salsa
Rehmannia glutinosa

Cross-Links

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PubChem 11972316
NPASS NPC215578