5,19-Epoxy-25-methoxycucurbita-6,23-dien-3-ol

Details

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Internal ID 8207cc89-8ede-4a2b-a8c9-ecb1844e9170
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Cucurbitacins
IUPAC Name (1R,4S,5S,8R,9R,12S,13S,16S)-8-[(E,2R)-6-methoxy-6-methylhept-4-en-2-yl]-5,9,17,17-tetramethyl-18-oxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-2-en-16-ol
SMILES (Canonical) CC(CC=CC(C)(C)OC)C1CCC2(C1(CCC34C2C=CC5(C3CCC(C5(C)C)O)OC4)C)C
SMILES (Isomeric) C[C@H](C/C=C/C(C)(C)OC)[C@H]1CC[C@@]2([C@@]1(CC[C@]34[C@H]2C=C[C@]5([C@H]3CC[C@@H](C5(C)C)O)OC4)C)C
InChI InChI=1S/C31H50O3/c1-21(10-9-15-26(2,3)33-8)22-13-16-29(7)23-14-17-31-24(11-12-25(32)27(31,4)5)30(23,20-34-31)19-18-28(22,29)6/h9,14-15,17,21-25,32H,10-13,16,18-20H2,1-8H3/b15-9+/t21-,22-,23+,24+,25+,28-,29+,30+,31-/m1/s1
InChI Key VQRZZBXVRJGWRS-VHZLPNKGSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C31H50O3
Molecular Weight 470.70 g/mol
Exact Mass 470.37599545 g/mol
Topological Polar Surface Area (TPSA) 38.70 Ų
XlogP 6.70
Atomic LogP (AlogP) 6.95
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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81910-39-6
AKOS040761163
FS-9065
(1R,4S,5S,8R,9R,12S,13S,16S)-8-[(E,2R)-6-methoxy-6-methylhept-4-en-2-yl]-5,9,17,17-tetramethyl-18-oxapentacyclo[10.5.2.01,13.04,12.05,9]nonadec-2-en-16-ol

2D Structure

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2D Structure of 5,19-Epoxy-25-methoxycucurbita-6,23-dien-3-ol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9959 99.59%
Caco-2 - 0.5996 59.96%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.6462 64.62%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8445 84.45%
OATP1B3 inhibitior + 0.9366 93.66%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6541 65.41%
BSEP inhibitior + 0.9636 96.36%
P-glycoprotein inhibitior + 0.5987 59.87%
P-glycoprotein substrate + 0.5907 59.07%
CYP3A4 substrate + 0.6890 68.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7076 70.76%
CYP3A4 inhibition - 0.8399 83.99%
CYP2C9 inhibition - 0.6188 61.88%
CYP2C19 inhibition - 0.7421 74.21%
CYP2D6 inhibition - 0.9533 95.33%
CYP1A2 inhibition - 0.8277 82.77%
CYP2C8 inhibition + 0.4922 49.22%
CYP inhibitory promiscuity - 0.8443 84.43%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6406 64.06%
Eye corrosion - 0.9875 98.75%
Eye irritation - 0.9505 95.05%
Skin irritation - 0.7672 76.72%
Skin corrosion - 0.9544 95.44%
Ames mutagenesis - 0.6370 63.70%
Human Ether-a-go-go-Related Gene inhibition + 0.8148 81.48%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation - 0.7769 77.69%
Respiratory toxicity + 0.6111 61.11%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6750 67.50%
Nephrotoxicity - 0.7053 70.53%
Acute Oral Toxicity (c) III 0.3663 36.63%
Estrogen receptor binding + 0.8592 85.92%
Androgen receptor binding + 0.7412 74.12%
Thyroid receptor binding + 0.6762 67.62%
Glucocorticoid receptor binding + 0.7528 75.28%
Aromatase binding + 0.7372 73.72%
PPAR gamma + 0.6416 64.16%
Honey bee toxicity - 0.6712 67.12%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9362 93.62%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 98.93% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 98.48% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 97.10% 97.25%
CHEMBL2581 P07339 Cathepsin D 96.42% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.06% 91.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 94.73% 95.89%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 91.01% 96.77%
CHEMBL5469 Q14289 Protein tyrosine kinase 2 beta 90.69% 91.03%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 88.42% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 88.26% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.21% 86.33%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.63% 97.09%
CHEMBL3922 P50579 Methionine aminopeptidase 2 85.76% 97.28%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.41% 91.07%
CHEMBL1907605 P24864 Cyclin-dependent kinase 2/cyclin E1 85.30% 92.88%
CHEMBL1744525 P43490 Nicotinamide phosphoribosyltransferase 82.95% 96.25%
CHEMBL1907602 P06493 Cyclin-dependent kinase 1/cyclin B1 82.91% 91.24%
CHEMBL5888 Q99558 Mitogen-activated protein kinase kinase kinase 14 82.75% 100.00%
CHEMBL1951 P21397 Monoamine oxidase A 82.57% 91.49%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 82.22% 92.62%
CHEMBL5028 O14672 ADAM10 82.12% 97.50%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 82.03% 98.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.89% 97.14%
CHEMBL2959 Q08881 Tyrosine-protein kinase ITK/TSK 81.80% 95.00%
CHEMBL233 P35372 Mu opioid receptor 81.08% 97.93%
CHEMBL2413 P32246 C-C chemokine receptor type 1 80.61% 89.50%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 80.56% 87.16%
CHEMBL2996 Q05655 Protein kinase C delta 80.38% 97.79%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.07% 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.
Momordica charantia

Cross-Links

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PubChem 91884853
LOTUS LTS0079790
wikiData Q105291462