2-(2,12-Dihydroxy-2,6,10-trimethyldodeca-6,10-dien-3-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol

Details

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Internal ID 8795714f-0e11-45c4-846b-d55bcccbb108
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name 2-(2,12-dihydroxy-2,6,10-trimethyldodeca-6,10-dien-3-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H38O8/c1-13(6-5-7-14(2)10-11-22)8-9-16(21(3,4)27)29-20-19(26)18(25)17(24)15(12-23)28-20/h6,10,15-20,22-27H,5,7-9,11-12H2,1-4H3
InChI Key GPZSEPAISCHICX-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C21H38O8
Molecular Weight 418.50 g/mol
Exact Mass 418.25666817 g/mol
Topological Polar Surface Area (TPSA) 140.00 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.39
H-Bond Acceptor 8
H-Bond Donor 6
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-(2,12-Dihydroxy-2,6,10-trimethyldodeca-6,10-dien-3-yl)oxy-6-(hydroxymethyl)oxane-3,4,5-triol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption - 0.5963 59.63%
Caco-2 - 0.7548 75.48%
Blood Brain Barrier - 0.5750 57.50%
Human oral bioavailability - 0.7000 70.00%
Subcellular localzation Mitochondria 0.8683 86.83%
OATP2B1 inhibitior - 0.8613 86.13%
OATP1B1 inhibitior + 0.9096 90.96%
OATP1B3 inhibitior + 0.8228 82.28%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.5250 52.50%
BSEP inhibitior + 0.5682 56.82%
P-glycoprotein inhibitior - 0.7116 71.16%
P-glycoprotein substrate - 0.8512 85.12%
CYP3A4 substrate + 0.6114 61.14%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8469 84.69%
CYP3A4 inhibition - 0.9270 92.70%
CYP2C9 inhibition - 0.7944 79.44%
CYP2C19 inhibition - 0.8063 80.63%
CYP2D6 inhibition - 0.9355 93.55%
CYP1A2 inhibition - 0.8389 83.89%
CYP2C8 inhibition - 0.7971 79.71%
CYP inhibitory promiscuity - 0.9283 92.83%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6768 67.68%
Eye corrosion - 0.9874 98.74%
Eye irritation - 0.9669 96.69%
Skin irritation - 0.7514 75.14%
Skin corrosion - 0.9632 96.32%
Ames mutagenesis - 0.7570 75.70%
Human Ether-a-go-go-Related Gene inhibition + 0.7089 70.89%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.7665 76.65%
skin sensitisation - 0.8311 83.11%
Respiratory toxicity - 0.7556 75.56%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6375 63.75%
Nephrotoxicity + 0.4838 48.38%
Acute Oral Toxicity (c) III 0.6500 65.00%
Estrogen receptor binding + 0.5776 57.76%
Androgen receptor binding - 0.6046 60.46%
Thyroid receptor binding + 0.6086 60.86%
Glucocorticoid receptor binding + 0.5996 59.96%
Aromatase binding + 0.5877 58.77%
PPAR gamma + 0.7646 76.46%
Honey bee toxicity - 0.7298 72.98%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.6900 69.00%
Fish aquatic toxicity + 0.8870 88.70%

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 96.09% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.69% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 93.66% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.57% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.60% 99.17%
CHEMBL2581 P07339 Cathepsin D 87.87% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 86.07% 93.56%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.46% 96.61%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.32% 96.47%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 85.21% 97.47%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 84.25% 95.89%

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.
Gynostemma yixingense

Cross-Links

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PubChem 163055317
LOTUS LTS0002116
wikiData Q105015272