2-[[8a-Methyl-4-methylidene-6-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-1,2,3,4a,5,6,7,8-octahydronaphthalen-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

Details

Top
Internal ID 9414572b-4719-4e49-93b2-42a88fa70615
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides
IUPAC Name 2-[[8a-methyl-4-methylidene-6-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-1,2,3,4a,5,6,7,8-octahydronaphthalen-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H46O12/c1-12-7-14(36-24-22(34)20(32)18(30)16(10-28)37-24)9-27(4)6-5-13(8-15(12)27)26(2,3)39-25-23(35)21(33)19(31)17(11-29)38-25/h13-25,28-35H,1,5-11H2,2-4H3
InChI Key UPFPPGMSXLZFBF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C27H46O12
Molecular Weight 562.60 g/mol
Exact Mass 562.29892690 g/mol
Topological Polar Surface Area (TPSA) 199.00 Ų
XlogP -0.80
Atomic LogP (AlogP) -1.46
H-Bond Acceptor 12
H-Bond Donor 8
Rotatable Bonds 7

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 2-[[8a-Methyl-4-methylidene-6-[2-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxypropan-2-yl]-1,2,3,4a,5,6,7,8-octahydronaphthalen-2-yl]oxy]-6-(hydroxymethyl)oxane-3,4,5-triol

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5599 55.99%
Caco-2 - 0.8819 88.19%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.8571 85.71%
Subcellular localzation Mitochondria 0.7588 75.88%
OATP2B1 inhibitior - 0.7232 72.32%
OATP1B1 inhibitior + 0.8651 86.51%
OATP1B3 inhibitior - 0.3000 30.00%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.5750 57.50%
BSEP inhibitior - 0.9151 91.51%
P-glycoprotein inhibitior - 0.5105 51.05%
P-glycoprotein substrate - 0.7680 76.80%
CYP3A4 substrate + 0.6726 67.26%
CYP2C9 substrate - 0.8025 80.25%
CYP2D6 substrate - 0.8264 82.64%
CYP3A4 inhibition - 0.9356 93.56%
CYP2C9 inhibition - 0.8338 83.38%
CYP2C19 inhibition - 0.8323 83.23%
CYP2D6 inhibition - 0.9397 93.97%
CYP1A2 inhibition - 0.8447 84.47%
CYP2C8 inhibition + 0.4927 49.27%
CYP inhibitory promiscuity - 0.9303 93.03%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6860 68.60%
Eye corrosion - 0.9882 98.82%
Eye irritation - 0.9220 92.20%
Skin irritation - 0.6656 66.56%
Skin corrosion - 0.9480 94.80%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4059 40.59%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation - 0.8809 88.09%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity - 0.6527 65.27%
Acute Oral Toxicity (c) III 0.6842 68.42%
Estrogen receptor binding + 0.5731 57.31%
Androgen receptor binding + 0.6601 66.01%
Thyroid receptor binding + 0.5217 52.17%
Glucocorticoid receptor binding - 0.5272 52.72%
Aromatase binding + 0.5875 58.75%
PPAR gamma + 0.5574 55.74%
Honey bee toxicity - 0.6541 65.41%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 0.9676 96.76%

Targets

Top

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 99.04% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 99.00% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 95.75% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 93.41% 97.79%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.21% 96.09%
CHEMBL1871 P10275 Androgen Receptor 92.23% 96.43%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.03% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 90.58% 95.89%
CHEMBL241 Q14432 Phosphodiesterase 3A 88.70% 92.94%
CHEMBL1977 P11473 Vitamin D receptor 88.34% 99.43%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 87.77% 100.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.57% 100.00%
CHEMBL237 P41145 Kappa opioid receptor 86.14% 98.10%
CHEMBL1951 P21397 Monoamine oxidase A 86.10% 91.49%
CHEMBL218 P21554 Cannabinoid CB1 receptor 85.73% 96.61%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 83.46% 95.50%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.22% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.41% 89.00%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 81.33% 96.21%
CHEMBL259 P32245 Melanocortin receptor 4 81.32% 95.38%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.32% 86.33%

Plants that contains it

Top
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.
Atractylodes lancea

Cross-Links

Top
PubChem 14507483
LOTUS LTS0229619
wikiData Q105276769