Hebevinoside III

Details

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Internal ID 2b34d34d-39d2-49bb-a49b-6ef01343f238
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins > Cucurbitacin glycosides
IUPAC Name [3,4,5-trihydroxy-6-[[7-hydroxy-4,4,9,13,14-pentamethyl-17-(6-methylhept-5-en-2-yl)-3-(3,4,5-trihydroxyoxan-2-yl)oxy-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-16-yl]oxy]oxan-2-yl]methyl acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C43H70O13/c1-21(2)11-10-12-22(3)31-28(54-39-36(51)34(49)33(48)29(55-39)20-52-23(4)44)18-43(9)37-26(45)17-25-24(41(37,7)15-16-42(31,43)8)13-14-30(40(25,5)6)56-38-35(50)32(47)27(46)19-53-38/h11,17,22,24,26-39,45-51H,10,12-16,18-20H2,1-9H3
InChI Key ZSGIZQTTWRMUOQ-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C43H70O13
Molecular Weight 795.00 g/mol
Exact Mass 794.48164228 g/mol
Topological Polar Surface Area (TPSA) 205.00 Ų
XlogP 3.70
Atomic LogP (AlogP) 3.13
H-Bond Acceptor 13
H-Bond Donor 7
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Hebevinoside III

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8605 86.05%
Caco-2 - 0.8763 87.63%
Blood Brain Barrier - 0.6500 65.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.8527 85.27%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7995 79.95%
OATP1B3 inhibitior - 0.2502 25.02%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7276 72.76%
BSEP inhibitior + 0.8445 84.45%
P-glycoprotein inhibitior + 0.7729 77.29%
P-glycoprotein substrate + 0.5483 54.83%
CYP3A4 substrate + 0.7282 72.82%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8832 88.32%
CYP3A4 inhibition - 0.9575 95.75%
CYP2C9 inhibition - 0.8728 87.28%
CYP2C19 inhibition - 0.9158 91.58%
CYP2D6 inhibition - 0.9382 93.82%
CYP1A2 inhibition - 0.9176 91.76%
CYP2C8 inhibition + 0.6267 62.67%
CYP inhibitory promiscuity - 0.9500 95.00%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6023 60.23%
Eye corrosion - 0.9905 99.05%
Eye irritation - 0.9122 91.22%
Skin irritation - 0.5215 52.15%
Skin corrosion - 0.9429 94.29%
Ames mutagenesis - 0.6478 64.78%
Human Ether-a-go-go-Related Gene inhibition + 0.7154 71.54%
Micronuclear - 0.8500 85.00%
Hepatotoxicity - 0.7374 73.74%
skin sensitisation - 0.8899 88.99%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.9324 93.24%
Acute Oral Toxicity (c) III 0.5791 57.91%
Estrogen receptor binding + 0.7569 75.69%
Androgen receptor binding + 0.7266 72.66%
Thyroid receptor binding - 0.5310 53.10%
Glucocorticoid receptor binding + 0.7477 74.77%
Aromatase binding + 0.6453 64.53%
PPAR gamma + 0.7659 76.59%
Honey bee toxicity - 0.6906 69.06%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5555 55.55%
Fish aquatic toxicity + 0.9707 97.07%

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 98.60% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.49% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.03% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.05% 97.25%
CHEMBL3137262 O60341 LSD1/CoREST complex 93.35% 97.09%
CHEMBL2581 P07339 Cathepsin D 91.84% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 91.71% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 87.58% 95.89%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.30% 100.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.15% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.66% 89.00%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 86.43% 92.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.38% 95.50%
CHEMBL5255 O00206 Toll-like receptor 4 84.69% 92.50%
CHEMBL5028 O14672 ADAM10 84.65% 97.50%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 84.11% 85.14%
CHEMBL2842 P42345 Serine/threonine-protein kinase mTOR 83.47% 92.78%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.22% 86.33%
CHEMBL1937 Q92769 Histone deacetylase 2 82.78% 94.75%
CHEMBL1951 P21397 Monoamine oxidase A 82.30% 91.49%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.13% 100.00%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.72% 94.33%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.53% 93.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.71% 93.56%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 80.27% 96.90%
CHEMBL218 P21554 Cannabinoid CB1 receptor 80.11% 96.61%
CHEMBL3475 P05121 Plasminogen activator inhibitor-1 80.06% 83.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.03% 97.28%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 53463009
LOTUS LTS0248269
wikiData Q104202746