Dichapetalin J

Details

Top
Internal ID bf17d622-90da-4739-800f-d93c6cebf5c3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids > Limonoids
IUPAC Name (3S,5R)-3-[(1R,2R,3R,5R,6R,9S,14S,15R,17R,18S,19S)-3,17-dihydroxy-9-(4-methoxyphenyl)-2,6,14-trimethyl-8-oxahexacyclo[16.3.1.01,18.02,15.05,14.06,11]docos-11-en-19-yl]-5-[(E)-3-hydroxy-2-methylprop-1-enyl]oxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C39H52O7/c1-22(19-40)14-26-16-27(34(43)46-26)28-11-13-38-20-39(28,38)33(42)18-31-35(2)12-10-24-15-29(23-6-8-25(44-5)9-7-23)45-21-36(24,3)30(35)17-32(41)37(31,38)4/h6-10,14,26-33,40-42H,11-13,15-21H2,1-5H3/b22-14+/t26-,27-,28-,29-,30+,31+,32+,33+,35-,36-,37-,38+,39+/m0/s1
InChI Key KOTGYKATMONDCA-YZSQOBSSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

Top
Molecular Formula C39H52O7
Molecular Weight 632.80 g/mol
Exact Mass 632.37130399 g/mol
Topological Polar Surface Area (TPSA) 105.00 Ų
XlogP 5.20
Atomic LogP (AlogP) 5.92
H-Bond Acceptor 7
H-Bond Donor 3
Rotatable Bonds 5

Synonyms

Top
876610-27-4
14,18-Cyclocholesta-2,24-dieno(4,3-c)pyran-21-oic acid, 2',4,5',6'-tetrahydro-7,12,23,26-tetrahydroxy-6'-(4-methoxyphenyl)-4,8-dimethyl-, gamma-lactone, (4alpha,5alpha,6'alpha,7alpha,12beta,13alpha,17alpha,20S,23R,24E)-
CHEMBL448039

2D Structure

Top
2D Structure of Dichapetalin J

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9830 98.30%
Caco-2 - 0.8358 83.58%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6857 68.57%
Subcellular localzation Mitochondria 0.8339 83.39%
OATP2B1 inhibitior - 0.5784 57.84%
OATP1B1 inhibitior + 0.8229 82.29%
OATP1B3 inhibitior + 0.9449 94.49%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.9787 97.87%
P-glycoprotein inhibitior + 0.7599 75.99%
P-glycoprotein substrate + 0.6095 60.95%
CYP3A4 substrate + 0.7521 75.21%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7886 78.86%
CYP3A4 inhibition + 0.5843 58.43%
CYP2C9 inhibition - 0.7587 75.87%
CYP2C19 inhibition - 0.7422 74.22%
CYP2D6 inhibition - 0.9015 90.15%
CYP1A2 inhibition - 0.7326 73.26%
CYP2C8 inhibition + 0.7808 78.08%
CYP inhibitory promiscuity - 0.6625 66.25%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.5191 51.91%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9251 92.51%
Skin irritation - 0.6961 69.61%
Skin corrosion - 0.9412 94.12%
Ames mutagenesis - 0.6078 60.78%
Human Ether-a-go-go-Related Gene inhibition + 0.6968 69.68%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5573 55.73%
skin sensitisation - 0.8770 87.70%
Respiratory toxicity + 0.8333 83.33%
Reproductive toxicity + 0.9667 96.67%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.5069 50.69%
Acute Oral Toxicity (c) I 0.4293 42.93%
Estrogen receptor binding + 0.8268 82.68%
Androgen receptor binding + 0.7838 78.38%
Thyroid receptor binding - 0.4882 48.82%
Glucocorticoid receptor binding + 0.7761 77.61%
Aromatase binding + 0.6643 66.43%
PPAR gamma + 0.6976 69.76%
Honey bee toxicity - 0.6511 65.11%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9857 98.57%

Targets

Top

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 98.55% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 98.11% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.30% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.58% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.45% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 93.29% 85.14%
CHEMBL1994 P08235 Mineralocorticoid receptor 90.13% 100.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 89.87% 95.71%
CHEMBL2996 Q05655 Protein kinase C delta 89.35% 97.79%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.13% 86.33%
CHEMBL332 P03956 Matrix metalloproteinase-1 88.90% 94.50%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 86.72% 94.00%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 86.42% 93.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.29% 89.00%
CHEMBL226 P30542 Adenosine A1 receptor 86.14% 95.93%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.03% 93.99%
CHEMBL221 P23219 Cyclooxygenase-1 85.68% 90.17%
CHEMBL5608 Q16288 NT-3 growth factor receptor 85.15% 95.89%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 84.81% 92.62%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 84.60% 89.05%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 83.88% 86.92%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.31% 95.89%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.14% 94.45%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.59% 100.00%

Plants that contains it

Top
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.
Dichapetalum gelonioides

Cross-Links

Top
PubChem 11549096
LOTUS LTS0202471
wikiData Q105143988