Schleicherastatin 5

Details

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Internal ID 03ef5216-d4d5-476f-a70f-a8ebaeebd0ba
Taxonomy Lipids and lipid-like molecules > Steroids and steroid derivatives > Stigmastanes and derivatives
IUPAC Name (3S,8S,9S,10R,13R,14S,17R)-17-[(2S,3R,5R)-5-ethyl-3-hydroxy-6-methylheptan-2-yl]-3-hydroxy-10,13-dimethyl-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta[a]phenanthren-7-one
SMILES (Canonical) CCC(CC(C(C)C1CCC2C1(CCC3C2C(=O)C=C4C3(CCC(C4)O)C)C)O)C(C)C
SMILES (Isomeric) CC[C@H](C[C@H]([C@@H](C)[C@H]1CC[C@@H]2[C@@]1(CC[C@H]3[C@H]2C(=O)C=C4[C@@]3(CC[C@@H](C4)O)C)C)O)C(C)C
InChI InChI=1S/C29H48O3/c1-7-19(17(2)3)14-25(31)18(4)22-8-9-23-27-24(11-13-29(22,23)6)28(5)12-10-21(30)15-20(28)16-26(27)32/h16-19,21-25,27,30-31H,7-15H2,1-6H3/t18-,19+,21-,22+,23-,24-,25+,27-,28-,29+/m0/s1
InChI Key XWLHFTUCQDCSTJ-PNGDTKJZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C29H48O3
Molecular Weight 444.70 g/mol
Exact Mass 444.36034539 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 6.90
Atomic LogP (AlogP) 6.17
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 6

Synonyms

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256445-58-6
(3S,8S,9S,10R,13R,14S,17R)-17-((2S,3R,5R)-5-ethyl-3-hydroxy-6-methylheptan-2-yl)-3-hydroxy-10,13-dimethyl-1,2,3,4,8,9,11,12,14,15,16,17-dodecahydrocyclopenta(a)phenanthren-7-one
RefChem:69166
(3beta,22R)-3,22-Dihydroxystigmast-5-en-7-one
SCHLEICHERASTATIN 5
CHEBI:169002
DTXSID701266624
(3I(2),22R)-3,22-Dihydroxystigmast-5-en-7-one

2D Structure

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2D Structure of Schleicherastatin 5

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 - 0.5977 59.77%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.7545 75.45%
OATP2B1 inhibitior - 0.5876 58.76%
OATP1B1 inhibitior + 0.8326 83.26%
OATP1B3 inhibitior + 0.9880 98.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior + 0.6000 60.00%
BSEP inhibitior + 0.8005 80.05%
P-glycoprotein inhibitior + 0.5937 59.37%
P-glycoprotein substrate + 0.6578 65.78%
CYP3A4 substrate + 0.6987 69.87%
CYP2C9 substrate - 0.7411 74.11%
CYP2D6 substrate - 0.8673 86.73%
CYP3A4 inhibition - 0.7201 72.01%
CYP2C9 inhibition - 0.9078 90.78%
CYP2C19 inhibition - 0.8809 88.09%
CYP2D6 inhibition - 0.9352 93.52%
CYP1A2 inhibition - 0.9515 95.15%
CYP2C8 inhibition - 0.5857 58.57%
CYP inhibitory promiscuity - 0.5246 52.46%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5903 59.03%
Eye corrosion - 0.9954 99.54%
Eye irritation - 0.9487 94.87%
Skin irritation + 0.6123 61.23%
Skin corrosion - 0.9594 95.94%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6423 64.23%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6182 61.82%
skin sensitisation - 0.5875 58.75%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.9875 98.75%
Nephrotoxicity - 0.8895 88.95%
Acute Oral Toxicity (c) III 0.5745 57.45%
Estrogen receptor binding + 0.8117 81.17%
Androgen receptor binding + 0.8571 85.71%
Thyroid receptor binding + 0.6014 60.14%
Glucocorticoid receptor binding + 0.7656 76.56%
Aromatase binding + 0.5516 55.16%
PPAR gamma + 0.5776 57.76%
Honey bee toxicity - 0.8198 81.98%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity + 0.9957 99.57%

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
CHEMBL2581 P07339 Cathepsin D 98.71% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 98.28% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 98.13% 95.93%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.06% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 93.76% 91.11%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 92.61% 90.71%
CHEMBL1994 P08235 Mineralocorticoid receptor 91.63% 100.00%
CHEMBL3137262 O60341 LSD1/CoREST complex 89.77% 97.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 89.05% 95.89%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 87.20% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.13% 94.45%
CHEMBL255 P29275 Adenosine A2b receptor 86.50% 98.59%
CHEMBL1806 P11388 DNA topoisomerase II alpha 84.16% 89.00%
CHEMBL221 P23219 Cyclooxygenase-1 83.70% 90.17%
CHEMBL1871 P10275 Androgen Receptor 82.70% 96.43%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.69% 86.33%
CHEMBL3746 P80365 11-beta-hydroxysteroid dehydrogenase 2 82.52% 94.78%
CHEMBL4208 P20618 Proteasome component C5 81.96% 90.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.07% 95.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.62% 93.04%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.52% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 80.32% 82.69%

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.
Schleichera oleosa

Cross-Links

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PubChem 11797567
LOTUS LTS0021032
wikiData Q105343538