Sinocalycanchinensin E

Details

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Internal ID 440e3e6f-62c3-44d4-a8e5-730110c27972
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones
IUPAC Name methyl 3-[(1S,4R,5R,8S,9S,12S,13R)-12-ethenyl-4,8-dimethyl-5-[(1S)-1-[(2R)-5-methyl-6-oxo-2,3-dihydropyran-2-yl]ethyl]-13-tetracyclo[7.5.0.01,13.04,8]tetradecanyl]propanoate
SMILES (Canonical) CC1=CCC(OC1=O)C(C)C2CCC3(C2(CCC45C3CCC(C4(C5)CCC(=O)OC)C=C)C)C
SMILES (Isomeric) CC1=CC[C@@H](OC1=O)[C@@H](C)[C@H]2CC[C@@]3([C@@]2(CC[C@]45[C@H]3CC[C@H]([C@]4(C5)CCC(=O)OC)C=C)C)C
InChI InChI=1S/C30H44O4/c1-7-21-9-11-24-28(5)14-12-22(20(3)23-10-8-19(2)26(32)34-23)27(28,4)16-17-30(24)18-29(21,30)15-13-25(31)33-6/h7-8,20-24H,1,9-18H2,2-6H3/t20-,21+,22+,23+,24-,27+,28-,29+,30-/m0/s1
InChI Key QNZKHYAIUBIBMQ-BDJJLNNZSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H44O4
Molecular Weight 468.70 g/mol
Exact Mass 468.32395988 g/mol
Topological Polar Surface Area (TPSA) 52.60 Ų
XlogP 7.90
Atomic LogP (AlogP) 6.64
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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CHEMBL1774189

2D Structure

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2D Structure of Sinocalycanchinensin E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9802 98.02%
Caco-2 - 0.5783 57.83%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability + 0.5571 55.71%
Subcellular localzation Mitochondria 0.6542 65.42%
OATP2B1 inhibitior - 0.7197 71.97%
OATP1B1 inhibitior + 0.8149 81.49%
OATP1B3 inhibitior + 0.9267 92.67%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.9508 95.08%
P-glycoprotein inhibitior + 0.7310 73.10%
P-glycoprotein substrate + 0.5486 54.86%
CYP3A4 substrate + 0.6960 69.60%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9063 90.63%
CYP3A4 inhibition - 0.6629 66.29%
CYP2C9 inhibition - 0.8405 84.05%
CYP2C19 inhibition - 0.8339 83.39%
CYP2D6 inhibition - 0.9507 95.07%
CYP1A2 inhibition - 0.7052 70.52%
CYP2C8 inhibition + 0.6489 64.89%
CYP inhibitory promiscuity - 0.7919 79.19%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.7293 72.93%
Eye corrosion - 0.9904 99.04%
Eye irritation - 0.9394 93.94%
Skin irritation - 0.6011 60.11%
Skin corrosion - 0.9380 93.80%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7590 75.90%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.5209 52.09%
skin sensitisation - 0.7693 76.93%
Respiratory toxicity + 0.7222 72.22%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7750 77.50%
Nephrotoxicity - 0.6076 60.76%
Acute Oral Toxicity (c) III 0.5545 55.45%
Estrogen receptor binding + 0.8160 81.60%
Androgen receptor binding + 0.7062 70.62%
Thyroid receptor binding + 0.5978 59.78%
Glucocorticoid receptor binding + 0.8158 81.58%
Aromatase binding + 0.7771 77.71%
PPAR gamma + 0.7008 70.08%
Honey bee toxicity - 0.7723 77.23%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5400 54.00%
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 98.80% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.76% 97.25%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 95.73% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.63% 95.56%
CHEMBL2581 P07339 Cathepsin D 91.18% 98.95%
CHEMBL4208 P20618 Proteasome component C5 89.68% 90.00%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 89.29% 91.07%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.12% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 86.11% 90.17%
CHEMBL3492 P49721 Proteasome Macropain subunit 85.59% 90.24%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 85.42% 97.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.95% 95.89%
CHEMBL4227 P25090 Lipoxin A4 receptor 84.94% 100.00%
CHEMBL5028 O14672 ADAM10 83.54% 97.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.08% 86.33%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 82.00% 95.71%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 81.65% 92.62%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 81.62% 93.00%
CHEMBL1937 Q92769 Histone deacetylase 2 81.61% 94.75%
CHEMBL340 P08684 Cytochrome P450 3A4 81.19% 91.19%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.00% 93.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.51% 97.09%
CHEMBL3401 O75469 Pregnane X receptor 80.43% 94.73%

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.
Calycanthus chinensis

Cross-Links

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PubChem 54581329
LOTUS LTS0271743
wikiData Q105224737