Dichapetalin K

Details

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Internal ID 76d8175d-3939-42ac-b536-bc9218ca66f1
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Triterpenoids
IUPAC Name (3S,5R)-3-[(1S,2R,3R,5R,6R,9S,14S,15R,18S,19S)-3-hydroxy-9-(4-methoxyphenyl)-2,6,14-trimethyl-8-oxahexacyclo[16.3.1.01,18.02,15.05,14.06,11]docosa-11,16-dien-19-yl]-5-[(E)-3-hydroxy-2-methylprop-1-enyl]oxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C39H50O6/c1-23(20-40)16-27-18-28(34(42)45-27)29-11-15-39-21-38(29,39)14-12-31-35(2)13-10-25-17-30(24-6-8-26(43-5)9-7-24)44-22-36(25,3)32(35)19-33(41)37(31,39)4/h6-10,12,14,16,27-33,40-41H,11,13,15,17-22H2,1-5H3/b23-16+/t27-,28-,29-,30-,31+,32+,33+,35+,36-,37-,38+,39+/m0/s1
InChI Key TUJRURFPAUTAHC-OJWYEGDGSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C39H50O6
Molecular Weight 614.80 g/mol
Exact Mass 614.36073931 g/mol
Topological Polar Surface Area (TPSA) 85.20 Ų
XlogP 6.30
Atomic LogP (AlogP) 6.73
H-Bond Acceptor 6
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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876610-29-6
14,18-Cyclocholesta-2,11,24-trieno(4,3-c)pyran-21-oic acid, 2',4,5',6'-tetrahydro-7,23,26-trihydroxy-6'-(4-methoxyphenyl)-4,8-dimethyl-, gamma-lactone, (4alpha,5alpha,6'alpha,7alpha,13alpha,17alpha,20S,23R,24E)-
CHEMBL502745

2D Structure

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2D Structure of Dichapetalin K

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9766 97.66%
Caco-2 - 0.8161 81.61%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8222 82.22%
OATP2B1 inhibitior - 0.7197 71.97%
OATP1B1 inhibitior + 0.8154 81.54%
OATP1B3 inhibitior + 0.9630 96.30%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9934 99.34%
P-glycoprotein inhibitior + 0.7989 79.89%
P-glycoprotein substrate + 0.6443 64.43%
CYP3A4 substrate + 0.7587 75.87%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8005 80.05%
CYP3A4 inhibition + 0.6375 63.75%
CYP2C9 inhibition - 0.7937 79.37%
CYP2C19 inhibition - 0.7397 73.97%
CYP2D6 inhibition - 0.8884 88.84%
CYP1A2 inhibition - 0.7205 72.05%
CYP2C8 inhibition + 0.8195 81.95%
CYP inhibitory promiscuity - 0.6374 63.74%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9200 92.00%
Carcinogenicity (trinary) Non-required 0.4807 48.07%
Eye corrosion - 0.9892 98.92%
Eye irritation - 0.9265 92.65%
Skin irritation - 0.6797 67.97%
Skin corrosion - 0.9411 94.11%
Ames mutagenesis - 0.6140 61.40%
Human Ether-a-go-go-Related Gene inhibition + 0.7042 70.42%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5948 59.48%
skin sensitisation - 0.8727 87.27%
Respiratory toxicity + 0.8556 85.56%
Reproductive toxicity + 0.9333 93.33%
Mitochondrial toxicity + 0.7625 76.25%
Nephrotoxicity + 0.5625 56.25%
Acute Oral Toxicity (c) I 0.4353 43.53%
Estrogen receptor binding + 0.8313 83.13%
Androgen receptor binding + 0.7793 77.93%
Thyroid receptor binding + 0.5682 56.82%
Glucocorticoid receptor binding + 0.8122 81.22%
Aromatase binding + 0.6438 64.38%
PPAR gamma + 0.7123 71.23%
Honey bee toxicity - 0.6437 64.37%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.9834 98.34%

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 98.93% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 98.16% 97.09%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.26% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.74% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.60% 85.14%
CHEMBL2581 P07339 Cathepsin D 95.27% 98.95%
CHEMBL226 P30542 Adenosine A1 receptor 93.79% 95.93%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.31% 94.45%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 91.21% 93.00%
CHEMBL4051 P13569 Cystic fibrosis transmembrane conductance regulator 90.98% 95.71%
CHEMBL4681 P42330 Aldo-keto-reductase family 1 member C3 90.87% 89.05%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.06% 86.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.91% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 88.87% 90.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 88.53% 92.62%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.24% 89.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 87.05% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 86.65% 95.89%
CHEMBL3192 Q9BY41 Histone deacetylase 8 86.24% 93.99%
CHEMBL2243 O00519 Anandamide amidohydrolase 85.95% 97.53%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 85.81% 91.07%
CHEMBL255 P29275 Adenosine A2b receptor 85.44% 98.59%
CHEMBL1907603 Q05586 Glutamate NMDA receptor; GRIN1/GRIN2B 83.84% 95.89%
CHEMBL2996 Q05655 Protein kinase C delta 83.56% 97.79%
CHEMBL3820 P35557 Hexokinase type IV 81.86% 91.96%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 81.15% 97.14%
CHEMBL3922 P50579 Methionine aminopeptidase 2 80.94% 97.28%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 80.78% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.47% 99.23%

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.
Dichapetalum gelonioides

Cross-Links

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PubChem 11585309
LOTUS LTS0206177
wikiData Q105264811