(25r)-5alpha-Spirostane-3,6-dione

Details

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Internal ID f47efafb-de2e-404f-9a6d-956d78a97ba6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (1R,2S,4S,5'R,6R,7S,8R,9S,12S,13R,18S)-5',7,9,13-tetramethylspiro[5-oxapentacyclo[10.8.0.02,9.04,8.013,18]icosane-6,2'-oxane]-16,19-dione
SMILES (Canonical) CC1CCC2(C(C3C(O2)CC4C3(CCC5C4CC(=O)C6C5(CCC(=O)C6)C)C)C)OC1
SMILES (Isomeric) C[C@@H]1CC[C@@]2([C@H]([C@H]3[C@@H](O2)C[C@@H]4[C@@]3(CC[C@H]5[C@H]4CC(=O)[C@@H]6[C@@]5(CCC(=O)C6)C)C)C)OC1
InChI InChI=1S/C27H40O4/c1-15-5-10-27(30-14-15)16(2)24-23(31-27)13-20-18-12-22(29)21-11-17(28)6-8-25(21,3)19(18)7-9-26(20,24)4/h15-16,18-21,23-24H,5-14H2,1-4H3/t15-,16+,18-,19+,20+,21-,23+,24+,25-,26+,27-/m1/s1
InChI Key CGXQJOWMWZPOPV-VNDFWDEUSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C27H40O4
Molecular Weight 428.60 g/mol
Exact Mass 428.29265975 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 4.40
Atomic LogP (AlogP) 5.18
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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SCHEMBL16039251
DTXSID501306802
Spirostan-3,6-dione, (5alpha,25R)-
3514-59-8

2D Structure

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2D Structure of (25r)-5alpha-Spirostane-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 + 0.9813 98.13%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.7813 78.13%
OATP2B1 inhibitior - 0.7141 71.41%
OATP1B1 inhibitior + 0.8959 89.59%
OATP1B3 inhibitior + 0.9603 96.03%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior + 0.7184 71.84%
P-glycoprotein inhibitior + 0.6255 62.55%
P-glycoprotein substrate - 0.6309 63.09%
CYP3A4 substrate + 0.7034 70.34%
CYP2C9 substrate - 0.7818 78.18%
CYP2D6 substrate - 0.7984 79.84%
CYP3A4 inhibition - 0.8920 89.20%
CYP2C9 inhibition - 0.9028 90.28%
CYP2C19 inhibition - 0.9008 90.08%
CYP2D6 inhibition - 0.9375 93.75%
CYP1A2 inhibition - 0.9085 90.85%
CYP2C8 inhibition - 0.5947 59.47%
CYP inhibitory promiscuity - 0.9711 97.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.6772 67.72%
Eye corrosion - 0.9793 97.93%
Eye irritation - 0.9423 94.23%
Skin irritation - 0.7543 75.43%
Skin corrosion - 0.8673 86.73%
Ames mutagenesis - 0.6770 67.70%
Human Ether-a-go-go-Related Gene inhibition - 0.5290 52.90%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.6073 60.73%
skin sensitisation - 0.9068 90.68%
Respiratory toxicity + 0.7889 78.89%
Reproductive toxicity + 0.6444 64.44%
Mitochondrial toxicity - 0.5125 51.25%
Nephrotoxicity - 0.6578 65.78%
Acute Oral Toxicity (c) III 0.7041 70.41%
Estrogen receptor binding + 0.7829 78.29%
Androgen receptor binding + 0.6307 63.07%
Thyroid receptor binding + 0.6342 63.42%
Glucocorticoid receptor binding + 0.8254 82.54%
Aromatase binding + 0.7268 72.68%
PPAR gamma + 0.5564 55.64%
Honey bee toxicity - 0.5381 53.81%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.9455 94.55%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 96.37% 97.09%
CHEMBL1914 P06276 Butyrylcholinesterase 92.55% 95.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 92.43% 100.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.80% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 90.56% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.06% 91.11%
CHEMBL6136 O60341 Lysine-specific histone demethylase 1 88.06% 95.58%
CHEMBL1902 P62942 FK506-binding protein 1A 87.60% 97.05%
CHEMBL5255 O00206 Toll-like receptor 4 87.10% 92.50%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.99% 93.04%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.17% 95.56%
CHEMBL1871 P10275 Androgen Receptor 84.38% 96.43%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.33% 89.00%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 84.00% 85.11%
CHEMBL4685 P14902 Indoleamine 2,3-dioxygenase 82.84% 96.38%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 82.82% 96.77%
CHEMBL236 P41143 Delta opioid receptor 81.98% 99.35%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.74% 97.14%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.60% 99.23%
CHEMBL4523377 Q86WV6 Stimulator of interferon genes protein 81.18% 95.48%
CHEMBL325 Q13547 Histone deacetylase 1 80.98% 95.92%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 80.59% 93.40%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 80.52% 89.05%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 80.43% 100.00%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 80.40% 94.78%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.35% 95.89%

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.
Solanum torvum

Cross-Links

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PubChem 10788676
LOTUS LTS0233402
wikiData Q104958389