(23E)-3beta-(beta-D-Glucopyranosyloxy)-7beta,25-dimethoxycucurbita-5,23-diene-19-al

Details

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Internal ID ea4abd27-b5dd-47a5-b763-0d40cbe8674a
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Steroidal glycosides > Steroidal saponins > Cucurbitacin glycosides
IUPAC Name (3S,7S,8S,9R,10R,13R,14S,17R)-7-methoxy-17-[(E,2R)-6-methoxy-6-methylhept-4-en-2-yl]-4,4,13,14-tetramethyl-3-[(2R,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-2,3,7,8,10,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-9-carbaldehyde
SMILES (Canonical) CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC3(C2C(C=C4C3CCC(C4(C)C)OC5C(C(C(C(O5)CO)O)O)O)OC)C=O)C)C
SMILES (Isomeric) C[C@H](C/C=C/C(C)(C)OC)[C@H]1CC[C@@]2([C@@]1(CC[C@@]3([C@H]2[C@H](C=C4[C@H]3CC[C@@H](C4(C)C)O[C@H]5[C@@H]([C@H]([C@@H]([C@H](O5)CO)O)O)O)OC)C=O)C)C
InChI InChI=1S/C38H62O9/c1-22(11-10-15-34(2,3)45-9)23-14-16-37(7)32-26(44-8)19-25-24(38(32,21-40)18-17-36(23,37)6)12-13-28(35(25,4)5)47-33-31(43)30(42)29(41)27(20-39)46-33/h10,15,19,21-24,26-33,39,41-43H,11-14,16-18,20H2,1-9H3/b15-10+/t22-,23-,24-,26+,27-,28+,29-,30+,31-,32+,33+,36-,37+,38-/m1/s1
InChI Key CHJLMGVNNACJNJ-ZEKNHKQRSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C38H62O9
Molecular Weight 662.90 g/mol
Exact Mass 662.43938355 g/mol
Topological Polar Surface Area (TPSA) 135.00 Ų
XlogP 4.20
Atomic LogP (AlogP) 4.59
H-Bond Acceptor 9
H-Bond Donor 4
Rotatable Bonds 10

Synonyms

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CHEMBL400959

2D Structure

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2D Structure of (23E)-3beta-(beta-D-Glucopyranosyloxy)-7beta,25-dimethoxycucurbita-5,23-diene-19-al

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8700 87.00%
Caco-2 - 0.8528 85.28%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.8286 82.86%
Subcellular localzation Mitochondria 0.8505 85.05%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7914 79.14%
OATP1B3 inhibitior - 0.2522 25.22%
MATE1 inhibitior - 0.9612 96.12%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior + 0.7062 70.62%
P-glycoprotein inhibitior + 0.7680 76.80%
P-glycoprotein substrate + 0.5581 55.81%
CYP3A4 substrate + 0.7139 71.39%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8371 83.71%
CYP3A4 inhibition - 0.9129 91.29%
CYP2C9 inhibition - 0.7964 79.64%
CYP2C19 inhibition - 0.8644 86.44%
CYP2D6 inhibition - 0.9329 93.29%
CYP1A2 inhibition - 0.7852 78.52%
CYP2C8 inhibition + 0.6072 60.72%
CYP inhibitory promiscuity - 0.8744 87.44%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6980 69.80%
Eye corrosion - 0.9899 98.99%
Eye irritation - 0.9245 92.45%
Skin irritation - 0.5929 59.29%
Skin corrosion - 0.9466 94.66%
Ames mutagenesis - 0.6300 63.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6896 68.96%
Micronuclear - 0.8200 82.00%
Hepatotoxicity - 0.6823 68.23%
skin sensitisation - 0.9019 90.19%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.7336 73.36%
Acute Oral Toxicity (c) III 0.6335 63.35%
Estrogen receptor binding + 0.6632 66.32%
Androgen receptor binding + 0.7451 74.51%
Thyroid receptor binding - 0.5349 53.49%
Glucocorticoid receptor binding + 0.7240 72.40%
Aromatase binding + 0.6521 65.21%
PPAR gamma + 0.6696 66.96%
Honey bee toxicity - 0.6921 69.21%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9553 95.53%

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 98.05% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.34% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.58% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.06% 97.25%
CHEMBL218 P21554 Cannabinoid CB1 receptor 92.60% 96.61%
CHEMBL5608 Q16288 NT-3 growth factor receptor 92.09% 95.89%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.23% 97.09%
CHEMBL3714130 P46095 G-protein coupled receptor 6 89.09% 97.36%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 87.68% 91.07%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.16% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.06% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.99% 97.14%
CHEMBL2581 P07339 Cathepsin D 85.61% 98.95%
CHEMBL3922 P50579 Methionine aminopeptidase 2 84.18% 97.28%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.11% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.64% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 83.51% 100.00%
CHEMBL3286 P00749 Urokinase-type plasminogen activator 83.45% 97.88%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.72% 92.62%
CHEMBL5028 O14672 ADAM10 81.13% 97.50%
CHEMBL4208 P20618 Proteasome component C5 81.07% 90.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.83% 96.00%

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.
Momordica charantia

Cross-Links

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PubChem 23626325
LOTUS LTS0265131
wikiData Q104958885