Hythiemoside A

Details

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Internal ID 2b06d3b6-62ee-4348-a42b-5042ce4a2b7b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene glycosides > Diterpene glycosides
IUPAC Name [(2R)-2-[(2S,4aR,4bS,7R,8aS)-2,4b,8,8-tetramethyl-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]-2-hydroxyethyl] acetate
SMILES (Canonical) CC(=O)OCC(C1(CCC2C(=C1)CCC3C2(CCC(C3(C)C)OC4C(C(C(C(O4)CO)O)O)O)C)C)O
SMILES (Isomeric) CC(=O)OC[C@@H]([C@]1(CC[C@@H]2C(=C1)CC[C@H]3[C@]2(CC[C@H](C3(C)C)O[C@H]4[C@@H]([C@H]([C@@H]([C@H](O4)CO)O)O)O)C)C)O
InChI InChI=1S/C28H46O9/c1-15(30)35-14-20(31)27(4)10-8-17-16(12-27)6-7-19-26(2,3)21(9-11-28(17,19)5)37-25-24(34)23(33)22(32)18(13-29)36-25/h12,17-25,29,31-34H,6-11,13-14H2,1-5H3/t17-,18-,19-,20+,21-,22-,23+,24-,25+,27+,28+/m1/s1
InChI Key ITRHSIFUIWDEGO-CHUAXZJFSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H46O9
Molecular Weight 526.70 g/mol
Exact Mass 526.31418304 g/mol
Topological Polar Surface Area (TPSA) 146.00 Ų
XlogP 2.20
Atomic LogP (AlogP) 1.67
H-Bond Acceptor 9
H-Bond Donor 5
Rotatable Bonds 6

Synonyms

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853267-91-1
[(2R)-2-[(2S,4aR,4bS,7R,8aS)-2,4b,8,8-tetramethyl-7-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4,4a,5,6,7,8a,9,10-octahydro-3H-phenanthren-2-yl]-2-hydroxyethyl] acetate
HY-N4023
AKOS032962203
CS-0024464
(2R,4aS,4bR,7S,10aS)-7-[(1R)-2-(Acetyloxy)-1-hydroxyethyl]-1,2,3,4,4a,4b,5,6,7,9,10,10a-dodecahydro-1,1,4a,7-tetramethyl-2-phenanthrenyl -D-glucopyranoside

2D Structure

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2D Structure of Hythiemoside A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8280 82.80%
Caco-2 - 0.7970 79.70%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8569 85.69%
OATP2B1 inhibitior - 0.7177 71.77%
OATP1B1 inhibitior + 0.8140 81.40%
OATP1B3 inhibitior - 0.5000 50.00%
MATE1 inhibitior - 0.9812 98.12%
OCT2 inhibitior - 0.6526 65.26%
BSEP inhibitior - 0.7093 70.93%
P-glycoprotein inhibitior - 0.4598 45.98%
P-glycoprotein substrate - 0.7738 77.38%
CYP3A4 substrate + 0.7001 70.01%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8827 88.27%
CYP3A4 inhibition - 0.8968 89.68%
CYP2C9 inhibition - 0.8549 85.49%
CYP2C19 inhibition - 0.8686 86.86%
CYP2D6 inhibition - 0.9356 93.56%
CYP1A2 inhibition - 0.8265 82.65%
CYP2C8 inhibition + 0.4545 45.45%
CYP inhibitory promiscuity - 0.9540 95.40%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6921 69.21%
Eye corrosion - 0.9903 99.03%
Eye irritation - 0.9448 94.48%
Skin irritation - 0.6263 62.63%
Skin corrosion - 0.9494 94.94%
Ames mutagenesis - 0.7370 73.70%
Human Ether-a-go-go-Related Gene inhibition + 0.6671 66.71%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.7050 70.50%
skin sensitisation - 0.8865 88.65%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.7903 79.03%
Acute Oral Toxicity (c) III 0.8000 80.00%
Estrogen receptor binding + 0.6244 62.44%
Androgen receptor binding + 0.6908 69.08%
Thyroid receptor binding - 0.5265 52.65%
Glucocorticoid receptor binding + 0.6236 62.36%
Aromatase binding + 0.6731 67.31%
PPAR gamma + 0.5326 53.26%
Honey bee toxicity - 0.7437 74.37%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9499 94.99%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.75% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.42% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.56% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 90.78% 97.09%
CHEMBL2581 P07339 Cathepsin D 90.73% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.62% 94.45%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.88% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 86.78% 95.89%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.57% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.12% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 85.94% 92.50%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.40% 99.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.10% 86.33%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 83.88% 92.62%
CHEMBL5028 O14672 ADAM10 83.55% 97.50%
CHEMBL4227 P25090 Lipoxin A4 receptor 83.44% 100.00%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 81.61% 91.24%
CHEMBL3714130 P46095 G-protein coupled receptor 6 80.93% 97.36%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 80.35% 98.75%

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.
Anisodus tanguticus
Cardopatium corymbosum
Lonchocarpus yucatanensis
Sidastrum tehuacanum
Sigesbeckia orientalis
Wollastonia biflora

Cross-Links

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PubChem 44607102
NPASS NPC120401
LOTUS LTS0128485
wikiData Q104399337