(1R,2R,4S,5S,9R,10S,12S,13R,14R,16R)-2,12,16-trihydroxy-5,9,14-trimethyl-5-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecan-15-one

Details

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Internal ID 07615198-d174-459b-a3b5-c3cb9da62297
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Diterpene glycosides
IUPAC Name (1R,2R,4S,5S,9R,10S,12S,13R,14R,16R)-2,12,16-trihydroxy-5,9,14-trimethyl-5-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecan-15-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C26H42O10/c1-11-17-12(28)7-15-25(3)6-4-5-24(2,14(25)8-16(29)26(15,21(11)33)22(17)34)10-35-23-20(32)19(31)18(30)13(9-27)36-23/h11-20,22-23,27-32,34H,4-10H2,1-3H3/t11-,12+,13-,14-,15+,16-,17-,18+,19+,20-,22-,23-,24-,25-,26+/m1/s1
InChI Key JQJBEHOGHZETSG-ZVEZQROKSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C26H42O10
Molecular Weight 514.60 g/mol
Exact Mass 514.27779753 g/mol
Topological Polar Surface Area (TPSA) 177.00 Ų
XlogP -0.50
Atomic LogP (AlogP) -1.06
H-Bond Acceptor 10
H-Bond Donor 7
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (1R,2R,4S,5S,9R,10S,12S,13R,14R,16R)-2,12,16-trihydroxy-5,9,14-trimethyl-5-[[(2R,3R,4S,5R,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxymethyl]tetracyclo[11.2.1.01,10.04,9]hexadecan-15-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.5810 58.10%
Caco-2 - 0.8290 82.90%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.6532 65.32%
OATP2B1 inhibitior - 0.5833 58.33%
OATP1B1 inhibitior + 0.8279 82.79%
OATP1B3 inhibitior + 0.9281 92.81%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.8755 87.55%
P-glycoprotein inhibitior - 0.5586 55.86%
P-glycoprotein substrate - 0.7874 78.74%
CYP3A4 substrate + 0.6779 67.79%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8495 84.95%
CYP3A4 inhibition - 0.9174 91.74%
CYP2C9 inhibition - 0.8721 87.21%
CYP2C19 inhibition - 0.8254 82.54%
CYP2D6 inhibition - 0.9625 96.25%
CYP1A2 inhibition - 0.8602 86.02%
CYP2C8 inhibition - 0.6268 62.68%
CYP inhibitory promiscuity - 0.9727 97.27%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9900 99.00%
Carcinogenicity (trinary) Non-required 0.7406 74.06%
Eye corrosion - 0.9922 99.22%
Eye irritation - 0.9553 95.53%
Skin irritation - 0.6451 64.51%
Skin corrosion - 0.9516 95.16%
Ames mutagenesis - 0.6424 64.24%
Human Ether-a-go-go-Related Gene inhibition - 0.4568 45.68%
Micronuclear - 0.9000 90.00%
Hepatotoxicity - 0.7649 76.49%
skin sensitisation - 0.9382 93.82%
Respiratory toxicity + 0.6222 62.22%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.7461 74.61%
Acute Oral Toxicity (c) I 0.5357 53.57%
Estrogen receptor binding + 0.6502 65.02%
Androgen receptor binding + 0.6850 68.50%
Thyroid receptor binding + 0.5255 52.55%
Glucocorticoid receptor binding + 0.5882 58.82%
Aromatase binding + 0.6785 67.85%
PPAR gamma + 0.5625 56.25%
Honey bee toxicity - 0.7804 78.04%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity - 0.6546 65.46%
Fish aquatic toxicity + 0.8318 83.18%

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 97.68% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.68% 97.09%
CHEMBL1937 Q92769 Histone deacetylase 2 93.48% 94.75%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.80% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.47% 98.95%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.81% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.01% 95.56%
CHEMBL5103 Q969S8 Histone deacetylase 10 86.31% 90.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.09% 86.33%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.91% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.65% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 83.92% 94.00%
CHEMBL5255 O00206 Toll-like receptor 4 83.67% 92.50%
CHEMBL220 P22303 Acetylcholinesterase 83.49% 94.45%
CHEMBL299 P17252 Protein kinase C alpha 83.25% 98.03%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.21% 100.00%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.11% 86.92%
CHEMBL3476 O15111 Inhibitor of nuclear factor kappa B kinase alpha subunit 82.92% 95.83%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.29% 95.50%
CHEMBL253 P34972 Cannabinoid CB2 receptor 81.13% 97.25%
CHEMBL4187 Q99250 Sodium channel protein type II alpha subunit 80.73% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.72% 94.45%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.24% 93.04%

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.
Isodon albopilosus

Cross-Links

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PubChem 162983309
LOTUS LTS0208839
wikiData Q105133510