6-[[10,21-Bis(hydroxymethyl)-2,5,6,10,14-pentamethyl-22-oxo-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-yl]oxy]-5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid

Details

Top
Internal ID 081131a9-df39-4006-bdd9-c41918361dca
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name 6-[[10,21-bis(hydroxymethyl)-2,5,6,10,14-pentamethyl-22-oxo-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-yl]oxy]-5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C48H74O20/c1-20-28(52)30(54)34(58)39(62-20)67-36-31(55)29(53)23(17-49)63-40(36)68-37-33(57)32(56)35(38(59)60)66-41(37)64-26-10-11-44(3)24(45(26,4)18-50)9-12-47(6)25(44)8-7-21-22-15-48(19-51)16-27(65-42(48)61)43(22,2)13-14-46(21,47)5/h7,20,22-37,39-41,49-58H,8-19H2,1-6H3,(H,59,60)
InChI Key OHGIOLTUWCTKCU-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

Top
Molecular Formula C48H74O20
Molecular Weight 971.10 g/mol
Exact Mass 970.47734475 g/mol
Topological Polar Surface Area (TPSA) 321.00 Ų
XlogP 1.00
Atomic LogP (AlogP) -0.78
H-Bond Acceptor 19
H-Bond Donor 11
Rotatable Bonds 10

Synonyms

Top
There are no found synonyms.

2D Structure

Top
2D Structure of 6-[[10,21-Bis(hydroxymethyl)-2,5,6,10,14-pentamethyl-22-oxo-23-oxahexacyclo[19.2.1.02,19.05,18.06,15.09,14]tetracos-17-en-11-yl]oxy]-5-[4,5-dihydroxy-6-(hydroxymethyl)-3-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxyoxan-2-yl]oxy-3,4-dihydroxyoxane-2-carboxylic acid

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7776 77.76%
Caco-2 - 0.8994 89.94%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.8429 84.29%
Subcellular localzation Mitochondria 0.8462 84.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8359 83.59%
OATP1B3 inhibitior + 0.8691 86.91%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5771 57.71%
BSEP inhibitior + 0.8070 80.70%
P-glycoprotein inhibitior + 0.7498 74.98%
P-glycoprotein substrate - 0.5553 55.53%
CYP3A4 substrate + 0.7296 72.96%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8832 88.32%
CYP3A4 inhibition - 0.9131 91.31%
CYP2C9 inhibition - 0.8486 84.86%
CYP2C19 inhibition - 0.8913 89.13%
CYP2D6 inhibition - 0.9479 94.79%
CYP1A2 inhibition - 0.8555 85.55%
CYP2C8 inhibition + 0.7473 74.73%
CYP inhibitory promiscuity - 0.9298 92.98%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5386 53.86%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.9054 90.54%
Skin irritation - 0.5261 52.61%
Skin corrosion - 0.9362 93.62%
Ames mutagenesis - 0.8400 84.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7223 72.23%
Micronuclear - 0.8000 80.00%
Hepatotoxicity - 0.7375 73.75%
skin sensitisation - 0.9227 92.27%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.7894 78.94%
Acute Oral Toxicity (c) III 0.5395 53.95%
Estrogen receptor binding + 0.7923 79.23%
Androgen receptor binding + 0.7389 73.89%
Thyroid receptor binding - 0.6127 61.27%
Glucocorticoid receptor binding + 0.7019 70.19%
Aromatase binding + 0.6241 62.41%
PPAR gamma + 0.7884 78.84%
Honey bee toxicity - 0.6966 69.66%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9755 97.55%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.10% 91.11%
CHEMBL3714130 P46095 G-protein coupled receptor 6 95.34% 97.36%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.08% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.56% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.03% 89.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 89.61% 93.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.74% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 86.09% 94.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.36% 97.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.68% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 83.47% 92.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.62% 99.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.43% 95.89%
CHEMBL2581 P07339 Cathepsin D 80.40% 98.95%

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.
There are no matching plants.

Cross-Links

Top
PubChem 85377177
LOTUS LTS0123198
wikiData Q105192066