Cipadesin J

Details

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Internal ID 8935cf44-ce90-43a4-901f-3a50beba1370
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name [(1R,2R,5S,6S,9R,11S,12S,13S,14R,17R,18R,20S,21R)-20-acetyloxy-6-(furan-3-yl)-13-hydroxy-1,5,12,17-tetramethyl-8-oxo-7,10,15-trioxahexacyclo[12.6.1.02,12.05,11.09,11.017,21]henicosan-18-yl] acetate
SMILES (Canonical) CC(=O)OC1CC(C2(C3CCC4(C(OC(=O)C5C4(C3(C(C6C2C1(CO6)C)O)C)O5)C7=COC=C7)C)C)OC(=O)C
SMILES (Isomeric) CC(=O)O[C@@H]1C[C@@H]([C@@]2([C@H]3CC[C@]4([C@@H](OC(=O)[C@H]5[C@]4([C@@]3([C@@H]([C@H]6[C@H]2[C@@]1(CO6)C)O)C)O5)C7=COC=C7)C)C)OC(=O)C
InChI InChI=1S/C30H38O10/c1-14(31)37-18-11-19(38-15(2)32)28(5)17-7-9-27(4)23(16-8-10-35-12-16)39-25(34)24-30(27,40-24)29(17,6)22(33)20-21(28)26(18,3)13-36-20/h8,10,12,17-24,33H,7,9,11,13H2,1-6H3/t17-,18-,19+,20-,21+,22-,23+,24+,26-,27+,28+,29+,30+/m1/s1
InChI Key LVAGOWFLIUIEFT-LAFZNRGESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C30H38O10
Molecular Weight 558.60 g/mol
Exact Mass 558.24649740 g/mol
Topological Polar Surface Area (TPSA) 134.00 Ų
XlogP 2.70
Atomic LogP (AlogP) 3.11
H-Bond Acceptor 10
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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CHEMBL1215107

2D Structure

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2D Structure of Cipadesin J

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9405 94.05%
Caco-2 - 0.7864 78.64%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.8190 81.90%
OATP2B1 inhibitior - 0.8603 86.03%
OATP1B1 inhibitior - 0.5000 50.00%
OATP1B3 inhibitior + 0.8448 84.48%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.9364 93.64%
P-glycoprotein inhibitior + 0.7298 72.98%
P-glycoprotein substrate + 0.5272 52.72%
CYP3A4 substrate + 0.7154 71.54%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8241 82.41%
CYP3A4 inhibition - 0.5858 58.58%
CYP2C9 inhibition - 0.7999 79.99%
CYP2C19 inhibition - 0.8390 83.90%
CYP2D6 inhibition - 0.9472 94.72%
CYP1A2 inhibition - 0.8197 81.97%
CYP2C8 inhibition + 0.7198 71.98%
CYP inhibitory promiscuity - 0.9157 91.57%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.5942 59.42%
Eye corrosion - 0.9896 98.96%
Eye irritation - 0.8740 87.40%
Skin irritation - 0.7104 71.04%
Skin corrosion - 0.9281 92.81%
Ames mutagenesis - 0.5819 58.19%
Human Ether-a-go-go-Related Gene inhibition + 0.6984 69.84%
Micronuclear - 0.6600 66.00%
Hepatotoxicity - 0.5447 54.47%
skin sensitisation - 0.9058 90.58%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.8444 84.44%
Mitochondrial toxicity + 0.7250 72.50%
Nephrotoxicity + 0.5738 57.38%
Acute Oral Toxicity (c) I 0.5304 53.04%
Estrogen receptor binding + 0.8356 83.56%
Androgen receptor binding + 0.7534 75.34%
Thyroid receptor binding + 0.6073 60.73%
Glucocorticoid receptor binding + 0.7577 75.77%
Aromatase binding + 0.7859 78.59%
PPAR gamma + 0.7405 74.05%
Honey bee toxicity - 0.7539 75.39%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5600 56.00%
Fish aquatic toxicity + 0.9852 98.52%

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 97.25% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.38% 96.09%
CHEMBL3137262 O60341 LSD1/CoREST complex 92.89% 97.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.60% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.05% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 89.80% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.99% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.75% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.27% 94.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 86.27% 82.69%
CHEMBL2581 P07339 Cathepsin D 85.16% 98.95%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 83.52% 100.00%
CHEMBL3922 P50579 Methionine aminopeptidase 2 83.24% 97.28%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.81% 95.56%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 80.55% 93.04%
CHEMBL340 P08684 Cytochrome P450 3A4 80.30% 91.19%

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.
Cipadessa baccifera

Cross-Links

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PubChem 46918555
LOTUS LTS0162654
wikiData Q105157749