(22e)-Stigmasta-4,22-diene-3,6-dione

Details

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Internal ID ed1e2a90-c934-4a35-bf55-7b471dfb1071
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Stigmastanes and derivatives
IUPAC Name (8S,9S,10R,13R,14S,17R)-17-[(E,2R,5S)-5-ethyl-6-methylhept-3-en-2-yl]-10,13-dimethyl-2,7,8,9,11,12,14,15,16,17-decahydro-1H-cyclopenta[a]phenanthrene-3,6-dione
SMILES (Canonical) CCC(C=CC(C)C1CCC2C1(CCC3C2CC(=O)C4=CC(=O)CCC34C)C)C(C)C
SMILES (Isomeric) CC[C@H](/C=C/[C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2CC(=O)C4=CC(=O)CC[C@]34C)C)C(C)C
InChI InChI=1S/C29H44O2/c1-7-20(18(2)3)9-8-19(4)23-10-11-24-22-17-27(31)26-16-21(30)12-14-29(26,6)25(22)13-15-28(23,24)5/h8-9,16,18-20,22-25H,7,10-15,17H2,1-6H3/b9-8+/t19-,20-,22+,23-,24+,25+,28-,29-/m1/s1
InChI Key XWHBTBBUPBKDBB-IZDHLYCQSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C29H44O2
Molecular Weight 424.70 g/mol
Exact Mass 424.334130642 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 7.60
Atomic LogP (AlogP) 7.19
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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Stigmasta-4,22-diene-3,6-dione
DTXSID901290106
50868-51-4

2D Structure

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2D Structure of (22e)-Stigmasta-4,22-diene-3,6-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.6567 65.67%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.7616 76.16%
OATP1B3 inhibitior + 0.9849 98.49%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.9533 95.33%
P-glycoprotein inhibitior + 0.8206 82.06%
P-glycoprotein substrate - 0.5878 58.78%
CYP3A4 substrate + 0.7090 70.90%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8671 86.71%
CYP3A4 inhibition - 0.8416 84.16%
CYP2C9 inhibition - 0.8675 86.75%
CYP2C19 inhibition - 0.5851 58.51%
CYP2D6 inhibition - 0.9365 93.65%
CYP1A2 inhibition - 0.9149 91.49%
CYP2C8 inhibition - 0.6276 62.76%
CYP inhibitory promiscuity - 0.5050 50.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5356 53.56%
Eye corrosion - 0.9886 98.86%
Eye irritation - 0.9640 96.40%
Skin irritation + 0.5077 50.77%
Skin corrosion - 0.9669 96.69%
Ames mutagenesis - 0.7914 79.14%
Human Ether-a-go-go-Related Gene inhibition + 0.7478 74.78%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5408 54.08%
skin sensitisation + 0.6737 67.37%
Respiratory toxicity + 0.9222 92.22%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.8625 86.25%
Nephrotoxicity - 0.9042 90.42%
Acute Oral Toxicity (c) III 0.7670 76.70%
Estrogen receptor binding + 0.8532 85.32%
Androgen receptor binding + 0.8031 80.31%
Thyroid receptor binding + 0.6313 63.13%
Glucocorticoid receptor binding + 0.8150 81.50%
Aromatase binding + 0.5812 58.12%
PPAR gamma + 0.6594 65.94%
Honey bee toxicity - 0.7009 70.09%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9959 99.59%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.37% 97.25%
CHEMBL2581 P07339 Cathepsin D 97.56% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.80% 96.09%
CHEMBL4224 P49759 Dual specificty protein kinase CLK1 95.33% 85.30%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 94.66% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.85% 91.11%
CHEMBL1994 P08235 Mineralocorticoid receptor 93.79% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.17% 97.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.76% 95.56%
CHEMBL4072 P07858 Cathepsin B 89.67% 93.67%
CHEMBL1871 P10275 Androgen Receptor 89.42% 96.43%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 88.92% 95.89%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 87.79% 82.69%
CHEMBL221 P23219 Cyclooxygenase-1 86.19% 90.17%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.20% 93.04%
CHEMBL202 P00374 Dihydrofolate reductase 84.91% 89.92%
CHEMBL236 P41143 Delta opioid receptor 84.87% 99.35%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.42% 85.14%
CHEMBL5203 P33316 dUTP pyrophosphatase 83.27% 99.18%
CHEMBL299 P17252 Protein kinase C alpha 82.21% 98.03%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.60% 97.14%
CHEMBL4227 P25090 Lipoxin A4 receptor 81.59% 100.00%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.57% 86.33%
CHEMBL1902 P62942 FK506-binding protein 1A 81.52% 97.05%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.39% 90.71%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 80.89% 92.86%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.80% 94.78%
CHEMBL237 P41145 Kappa opioid receptor 80.61% 98.10%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 80.07% 95.71%

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.
Conium maculatum
Frullania brasiliensis
Vitex trifolia

Cross-Links

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PubChem 10455054
NPASS NPC51331
LOTUS LTS0195091
wikiData Q105343394