Spiroscytalin

Details

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Internal ID 51c5a4aa-0b71-43c4-ace6-7625b5f5830a
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name (4S,4aR,5S,5'R,6S,8aR)-5'-benzyl-4,6-dimethylspiro[2,3,4,4a,6,8a-hexahydro-1H-naphthalene-5,3'-pyrrolidine]-2',4'-dione
SMILES (Canonical) CC1CCCC2C1C3(C(C=C2)C)C(=O)C(NC3=O)CC4=CC=CC=C4
SMILES (Isomeric) C[C@H]1CCC[C@H]2[C@@H]1[C@@]3([C@H](C=C2)C)C(=O)[C@H](NC3=O)CC4=CC=CC=C4
InChI InChI=1S/C22H27NO2/c1-14-7-6-10-17-12-11-15(2)22(19(14)17)20(24)18(23-21(22)25)13-16-8-4-3-5-9-16/h3-5,8-9,11-12,14-15,17-19H,6-7,10,13H2,1-2H3,(H,23,25)/t14-,15-,17+,18+,19+,22-/m0/s1
InChI Key ZUCYLMDAXHXTEP-BWGSOXPZSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C22H27NO2
Molecular Weight 337.50 g/mol
Exact Mass 337.204179104 g/mol
Topological Polar Surface Area (TPSA) 46.20 Ų
XlogP 4.90
Atomic LogP (AlogP) 3.54
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Spiroscytalin

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 + 0.5862 58.62%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.4169 41.69%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9079 90.79%
OATP1B3 inhibitior + 0.9465 94.65%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior + 0.5186 51.86%
BSEP inhibitior + 0.6471 64.71%
P-glycoprotein inhibitior - 0.5000 50.00%
P-glycoprotein substrate - 0.5491 54.91%
CYP3A4 substrate + 0.5723 57.23%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8162 81.62%
CYP3A4 inhibition - 0.8487 84.87%
CYP2C9 inhibition - 0.5870 58.70%
CYP2C19 inhibition + 0.5910 59.10%
CYP2D6 inhibition - 0.7960 79.60%
CYP1A2 inhibition - 0.5849 58.49%
CYP2C8 inhibition - 0.6272 62.72%
CYP inhibitory promiscuity + 0.7422 74.22%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.4871 48.71%
Eye corrosion - 0.9918 99.18%
Eye irritation - 0.9973 99.73%
Skin irritation - 0.7638 76.38%
Skin corrosion - 0.8966 89.66%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7596 75.96%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation - 0.8279 82.79%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.4830 48.30%
Acute Oral Toxicity (c) III 0.6149 61.49%
Estrogen receptor binding + 0.7714 77.14%
Androgen receptor binding + 0.6051 60.51%
Thyroid receptor binding + 0.5548 55.48%
Glucocorticoid receptor binding + 0.6016 60.16%
Aromatase binding + 0.6749 67.49%
PPAR gamma - 0.6950 69.50%
Honey bee toxicity - 0.8879 88.79%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.8404 84.04%

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 98.25% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.31% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.84% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 91.74% 90.17%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.15% 97.09%
CHEMBL2693 Q9UIQ6 Cystinyl aminopeptidase 91.13% 97.64%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 88.74% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.25% 86.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 85.11% 85.14%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.73% 82.69%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.36% 95.89%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 82.80% 93.03%
CHEMBL2535 P11166 Glucose transporter 81.77% 98.75%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 80.19% 94.62%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.10% 96.25%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139587811
LOTUS LTS0011252
wikiData Q77624588