NCGC00169820-03_C42H66O14_Hexopyranose, 1-O-[3-[(6-deoxyhexopyranosyl)oxy]-27-hydroxy-27,28-dioxoolean-12-en-28-yl]-

Details

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Internal ID 6371126e-a208-431f-9a2b-d4a3b9eb3337
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Triterpene glycosides > Triterpene saponins
IUPAC Name 2,2,6b,9,9,12a-hexamethyl-4a-[3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxycarbonyl-10-(3,4,5-trihydroxy-6-methyloxan-2-yl)oxy-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-6a-carboxylic acid
SMILES (Canonical) CC1C(C(C(C(O1)OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C(=O)O)C)C)O)O)O
SMILES (Isomeric) CC1C(C(C(C(O1)OC2CCC3(C(C2(C)C)CCC4(C3CC=C5C4(CCC6(C5CC(CC6)(C)C)C(=O)OC7C(C(C(C(O7)CO)O)O)O)C(=O)O)C)C)O)O)O
InChI InChI=1S/C42H66O14/c1-20-27(44)29(46)31(48)33(53-20)55-26-11-12-39(6)24(38(26,4)5)10-13-40(7)25(39)9-8-21-22-18-37(2,3)14-15-41(22,16-17-42(21,40)35(50)51)36(52)56-34-32(49)30(47)28(45)23(19-43)54-34/h8,20,22-34,43-49H,9-19H2,1-7H3,(H,50,51)
InChI Key ZCBRYYRPNSHPER-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C42H66O14
Molecular Weight 795.00 g/mol
Exact Mass 794.44525677 g/mol
Topological Polar Surface Area (TPSA) 233.00 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.41
H-Bond Acceptor 13
H-Bond Donor 8
Rotatable Bonds 6

Synonyms

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ACon1_002465
AKOS040738933
NCGC00169820-01
NCGC00169820-03
NCGC00169820-03_C42H66O14_Hexopyranose, 1-O-[3-[(6-deoxyhexopyranosyl)oxy]-27-hydroxy-27,28-dioxoolean-12-en-28-yl]-

2D Structure

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2D Structure of NCGC00169820-03_C42H66O14_Hexopyranose, 1-O-[3-[(6-deoxyhexopyranosyl)oxy]-27-hydroxy-27,28-dioxoolean-12-en-28-yl]-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.7941 79.41%
Caco-2 - 0.8738 87.38%
Blood Brain Barrier - 0.6000 60.00%
Human oral bioavailability - 0.7714 77.14%
Subcellular localzation Mitochondria 0.8948 89.48%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.6945 69.45%
OATP1B3 inhibitior - 0.5056 50.56%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior + 0.6474 64.74%
BSEP inhibitior + 0.7345 73.45%
P-glycoprotein inhibitior + 0.7497 74.97%
P-glycoprotein substrate - 0.7630 76.30%
CYP3A4 substrate + 0.7101 71.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8776 87.76%
CYP3A4 inhibition - 0.8459 84.59%
CYP2C9 inhibition - 0.8380 83.80%
CYP2C19 inhibition - 0.9220 92.20%
CYP2D6 inhibition - 0.9493 94.93%
CYP1A2 inhibition - 0.8499 84.99%
CYP2C8 inhibition + 0.6406 64.06%
CYP inhibitory promiscuity - 0.9381 93.81%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6298 62.98%
Eye corrosion - 0.9898 98.98%
Eye irritation - 0.9097 90.97%
Skin irritation - 0.5723 57.23%
Skin corrosion - 0.9450 94.50%
Ames mutagenesis - 0.7670 76.70%
Human Ether-a-go-go-Related Gene inhibition - 0.4165 41.65%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.8781 87.81%
skin sensitisation - 0.9064 90.64%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8889 88.89%
Mitochondrial toxicity - 0.6125 61.25%
Nephrotoxicity - 0.8651 86.51%
Acute Oral Toxicity (c) III 0.7628 76.28%
Estrogen receptor binding + 0.7314 73.14%
Androgen receptor binding + 0.7216 72.16%
Thyroid receptor binding - 0.5792 57.92%
Glucocorticoid receptor binding + 0.6587 65.87%
Aromatase binding + 0.6311 63.11%
PPAR gamma + 0.7228 72.28%
Honey bee toxicity - 0.7517 75.17%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5905 59.05%
Fish aquatic toxicity + 0.9778 97.78%

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 97.71% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.80% 96.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 93.43% 97.36%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.02% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 92.29% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 88.31% 90.17%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.51% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.83% 89.00%
CHEMBL2581 P07339 Cathepsin D 84.98% 98.95%
CHEMBL3880 P07900 Heat shock protein HSP 90-alpha 84.59% 96.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.87% 99.17%
CHEMBL1994 P08235 Mineralocorticoid receptor 81.95% 100.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.56% 94.45%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.52% 93.00%
CHEMBL5255 O00206 Toll-like receptor 4 80.97% 92.50%
CHEMBL5028 O14672 ADAM10 80.46% 97.50%

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.
Cephalanthus occidentalis
Isertia haenkeana
Uncaria tomentosa

Cross-Links

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PubChem 14466247
LOTUS LTS0028602
wikiData Q105370963