23,24-dihydrocucurbitacin E

Details

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Internal ID 25341d96-9949-4fda-bc04-af6b9e30cd96
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cucurbitacins
IUPAC Name [(6R)-6-[(8S,9R,10R,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxoheptan-2-yl] acetate
SMILES (Canonical) CC(=O)OC(C)(C)CCC(=O)C(C)(C1C(CC2(C1(CC(=O)C3(C2CC=C4C3C=C(C(=O)C4(C)C)O)C)C)C)O)O
SMILES (Isomeric) CC(=O)OC(C)(C)CCC(=O)[C@@](C)([C@H]1[C@@H](C[C@@]2([C@@]1(CC(=O)[C@@]3([C@H]2CC=C4[C@H]3C=C(C(=O)C4(C)C)O)C)C)C)O)O
InChI InChI=1S/C32H46O8/c1-17(33)40-27(2,3)13-12-23(36)32(9,39)25-21(35)15-29(6)22-11-10-18-19(14-20(34)26(38)28(18,4)5)31(22,8)24(37)16-30(25,29)7/h10,14,19,21-22,25,34-35,39H,11-13,15-16H2,1-9H3/t19-,21-,22+,25+,29+,30-,31+,32+/m1/s1
InChI Key XZBVNQWNPRMHRH-LAMASETHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C32H46O8
Molecular Weight 558.70 g/mol
Exact Mass 558.31926842 g/mol
Topological Polar Surface Area (TPSA) 138.00 Ų
XlogP 3.30
Atomic LogP (AlogP) 4.41
H-Bond Acceptor 8
H-Bond Donor 3
Rotatable Bonds 6

Synonyms

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Dihydrocucurbitacin E
28973-67-3
CHEBI:62228
(4R)-2,16alpha,20-trihydroxy-9beta,10,14-trimethyl-1,11,22-trioxo-4,9-cyclo-9,10-secocholesta-2,5-dien-25-yl acetate
[(6R)-6-[(8S,9R,10R,13R,14S,16R,17R)-2,16-dihydroxy-4,4,9,13,14-pentamethyl-3,11-dioxo-8,10,12,15,16,17-hexahydro-7H-cyclopenta[a]phenanthren-17-yl]-6-hydroxy-2-methyl-5-oxoheptan-2-yl] acetate
19-Norlanosta-1,5-diene-3,11,22-trione, 25-(acetyloxy)-2,16,20-trihydroxy-9-methyl-, (9beta,10alpha,16alpha)-
2,16alpha,20,25-tetrahydroxy-9-methyl-19-nor-9beta,10alpha-lanosta-1,5-diene-3,11,22-trione 25-acetate
25-acetyloxy-2,16alpha,20-trihydroxy-9beta-methyl-19-nor-10alpha-lanosta-1,5-diene-3,11,22-trione
22,23-dihydrocucurbitacin E
CHEMBL256519
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 23,24-dihydrocucurbitacin E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9842 98.42%
Caco-2 - 0.7259 72.59%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8335 83.35%
OATP2B1 inhibitior - 0.7183 71.83%
OATP1B1 inhibitior + 0.8513 85.13%
OATP1B3 inhibitior - 0.3834 38.34%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7782 77.82%
BSEP inhibitior + 0.8380 83.80%
P-glycoprotein inhibitior + 0.7064 70.64%
P-glycoprotein substrate + 0.5390 53.90%
CYP3A4 substrate + 0.7085 70.85%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.9063 90.63%
CYP3A4 inhibition - 0.7807 78.07%
CYP2C9 inhibition - 0.7748 77.48%
CYP2C19 inhibition - 0.8339 83.39%
CYP2D6 inhibition - 0.9511 95.11%
CYP1A2 inhibition - 0.8989 89.89%
CYP2C8 inhibition + 0.5854 58.54%
CYP inhibitory promiscuity - 0.8694 86.94%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.6960 69.60%
Eye corrosion - 0.9934 99.34%
Eye irritation - 0.9084 90.84%
Skin irritation + 0.6742 67.42%
Skin corrosion - 0.9441 94.41%
Ames mutagenesis - 0.6900 69.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5374 53.74%
Micronuclear - 0.7200 72.00%
Hepatotoxicity - 0.5662 56.62%
skin sensitisation - 0.8392 83.92%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity + 1.0000 100.00%
Mitochondrial toxicity + 0.9625 96.25%
Nephrotoxicity + 0.4740 47.40%
Acute Oral Toxicity (c) I 0.5681 56.81%
Estrogen receptor binding + 0.6967 69.67%
Androgen receptor binding + 0.7198 71.98%
Thyroid receptor binding + 0.6207 62.07%
Glucocorticoid receptor binding + 0.7807 78.07%
Aromatase binding + 0.7785 77.85%
PPAR gamma + 0.6167 61.67%
Honey bee toxicity - 0.6981 69.81%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.5400 54.00%
Fish aquatic toxicity + 0.9962 99.62%

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 98.78% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.01% 85.14%
CHEMBL2581 P07339 Cathepsin D 96.96% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.94% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 94.14% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 93.39% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 92.67% 97.25%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.91% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.72% 95.56%
CHEMBL3230 O95977 Sphingosine 1-phosphate receptor Edg-6 84.53% 94.01%
CHEMBL2996 Q05655 Protein kinase C delta 83.89% 97.79%
CHEMBL4208 P20618 Proteasome component C5 82.59% 90.00%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 81.53% 87.67%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.52% 100.00%

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.
Begonia nantoensis
Bryonia alba
Bryonia cretica
Wilbrandia ebracteata

Cross-Links

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PubChem 21577087
LOTUS LTS0055330
wikiData Q27131698