Schisanlactone A

Details

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Internal ID 5e00a2c4-9f27-45ec-ae70-bf4bc6557ad9
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name (9R,13R,16R,17R)-8,8,13,17-tetramethyl-16-[(1S)-1-[(2R)-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-7-oxatetracyclo[10.7.0.03,9.013,17]nonadeca-1(12),2,4-trien-6-one
SMILES (Canonical) CC1=CCC(OC1=O)C(C)C2CCC3(C2(CCC4=C3CCC5C(=C4)C=CC(=O)OC5(C)C)C)C
SMILES (Isomeric) CC1=CC[C@@H](OC1=O)[C@@H](C)[C@H]2CC[C@@]3([C@@]2(CCC4=C3CC[C@@H]5C(=C4)C=CC(=O)OC5(C)C)C)C
InChI InChI=1S/C30H40O4/c1-18-7-11-25(33-27(18)32)19(2)22-14-16-30(6)24-10-9-23-20(8-12-26(31)34-28(23,3)4)17-21(24)13-15-29(22,30)5/h7-8,12,17,19,22-23,25H,9-11,13-16H2,1-6H3/t19-,22+,23+,25+,29+,30-/m0/s1
InChI Key VJNOAOVMGNCSPJ-ZCTPSQTASA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C30H40O4
Molecular Weight 464.60 g/mol
Exact Mass 464.29265975 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 6.30
Atomic LogP (AlogP) 6.63
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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CHEBI:66431
(3R,3aR,11aR,13bR)-3a,11,11,13b-tetramethyl-3-{(1S)-1-[(2R)-5-methyl-6-oxo-3,6-dihydro-2H-pyran-2-yl]ethyl}-2,3,3a,4,5,11,11a,12,13,13b-decahydroindeno[5',4':4,5]cyclohepta[1,2-c]oxepin-9(1H)-one
CHEMBL487866
BDBM50479301
Q27134992

2D Structure

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2D Structure of Schisanlactone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9882 98.82%
Caco-2 - 0.5290 52.90%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7958 79.58%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.8243 82.43%
OATP1B3 inhibitior + 0.9598 95.98%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.9212 92.12%
P-glycoprotein inhibitior + 0.8981 89.81%
P-glycoprotein substrate + 0.5076 50.76%
CYP3A4 substrate + 0.6873 68.73%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9084 90.84%
CYP3A4 inhibition - 0.8215 82.15%
CYP2C9 inhibition - 0.8985 89.85%
CYP2C19 inhibition - 0.9345 93.45%
CYP2D6 inhibition - 0.9495 94.95%
CYP1A2 inhibition - 0.7911 79.11%
CYP2C8 inhibition + 0.6282 62.82%
CYP inhibitory promiscuity - 0.9376 93.76%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.6362 63.62%
Eye corrosion - 0.9924 99.24%
Eye irritation - 0.9446 94.46%
Skin irritation + 0.5055 50.55%
Skin corrosion - 0.8935 89.35%
Ames mutagenesis - 0.7400 74.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8610 86.10%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.6695 66.95%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.8667 86.67%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity + 0.7463 74.63%
Acute Oral Toxicity (c) III 0.6525 65.25%
Estrogen receptor binding + 0.8206 82.06%
Androgen receptor binding + 0.7758 77.58%
Thyroid receptor binding + 0.7050 70.50%
Glucocorticoid receptor binding + 0.8262 82.62%
Aromatase binding + 0.8062 80.62%
PPAR gamma + 0.6608 66.08%
Honey bee toxicity - 0.8022 80.22%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity + 0.9941 99.41%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.00% 91.11%
CHEMBL2581 P07339 Cathepsin D 95.77% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 95.66% 95.56%
CHEMBL253 P34972 Cannabinoid CB2 receptor 93.44% 97.25%
CHEMBL1937 Q92769 Histone deacetylase 2 93.22% 94.75%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 89.05% 97.14%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 88.41% 85.94%
CHEMBL3038469 P24941 CDK2/Cyclin A 88.12% 91.38%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.92% 97.09%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 87.20% 99.23%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.42% 100.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.93% 89.00%
CHEMBL1907600 Q00535 Cyclin-dependent kinase 5/CDK5 activator 1 83.51% 93.03%
CHEMBL5103 Q969S8 Histone deacetylase 10 82.81% 90.08%
CHEMBL221 P23219 Cyclooxygenase-1 82.39% 90.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.06% 85.14%
CHEMBL2553 Q15418 Ribosomal protein S6 kinase alpha 1 81.50% 85.11%
CHEMBL5608 Q16288 NT-3 growth factor receptor 81.18% 95.89%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 81.08% 95.50%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.87% 94.45%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.25% 94.00%
CHEMBL4444 P04070 Vitamin K-dependent protein C 80.18% 93.89%

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.
Helenium autumnale
Kadsura longepedunculata
Schisandra propinqua

Cross-Links

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PubChem 44560613
NPASS NPC166143
ChEMBL CHEMBL487866
LOTUS LTS0135654
wikiData Q27134992