Javanicolide E

Details

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Internal ID 88729e33-f96d-4b8f-a24f-6f6363fb3a07
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Quassinoids
IUPAC Name methyl (1R,2S,3R,6R,8S,9S,10R,13S,14R,15R,16S,17S)-10,15,16-trihydroxy-9,13-dimethyl-3-(3-methylbut-2-enoyloxy)-4,11-dioxo-5,18-dioxapentacyclo[12.5.0.01,6.02,17.08,13]nonadecane-17-carboxylate
SMILES (Canonical) CC1C2CC3C45COC(C4C(C(=O)O3)OC(=O)C=C(C)C)(C(C(C5C2(CC(=O)C1O)C)O)O)C(=O)OC
SMILES (Isomeric) C[C@H]1[C@@H]2C[C@@H]3[C@@]45CO[C@@]([C@@H]4[C@H](C(=O)O3)OC(=O)C=C(C)C)([C@H]([C@@H]([C@@H]5[C@]2(CC(=O)[C@@H]1O)C)O)O)C(=O)OC
InChI InChI=1S/C26H34O11/c1-10(2)6-15(28)37-18-20-25-9-35-26(20,23(33)34-5)21(31)17(30)19(25)24(4)8-13(27)16(29)11(3)12(24)7-14(25)36-22(18)32/h6,11-12,14,16-21,29-31H,7-9H2,1-5H3/t11-,12-,14+,16+,17+,18+,19+,20+,21-,24-,25+,26-/m0/s1
InChI Key BVRDRHRMMWTKQW-VXNVDJCPSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C26H34O11
Molecular Weight 522.50 g/mol
Exact Mass 522.21011190 g/mol
Topological Polar Surface Area (TPSA) 166.00 Ų
XlogP 1.00
Atomic LogP (AlogP) -0.32
H-Bond Acceptor 11
H-Bond Donor 3
Rotatable Bonds 3

Synonyms

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CHEMBL2037041

2D Structure

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2D Structure of Javanicolide E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9461 94.61%
Caco-2 - 0.7949 79.49%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.8150 81.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8543 85.43%
OATP1B3 inhibitior + 0.9194 91.94%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.9144 91.44%
P-glycoprotein inhibitior + 0.6452 64.52%
P-glycoprotein substrate + 0.8365 83.65%
CYP3A4 substrate + 0.7050 70.50%
CYP2C9 substrate - 0.8253 82.53%
CYP2D6 substrate - 0.8954 89.54%
CYP3A4 inhibition - 0.7852 78.52%
CYP2C9 inhibition - 0.7951 79.51%
CYP2C19 inhibition - 0.8467 84.67%
CYP2D6 inhibition - 0.9413 94.13%
CYP1A2 inhibition - 0.8327 83.27%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.9291 92.91%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.5617 56.17%
Eye corrosion - 0.9887 98.87%
Eye irritation - 0.9234 92.34%
Skin irritation - 0.6481 64.81%
Skin corrosion - 0.9390 93.90%
Ames mutagenesis - 0.5000 50.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5347 53.47%
Micronuclear - 0.6400 64.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8465 84.65%
Respiratory toxicity + 0.8000 80.00%
Reproductive toxicity + 0.9000 90.00%
Mitochondrial toxicity + 0.7125 71.25%
Nephrotoxicity + 0.7148 71.48%
Acute Oral Toxicity (c) I 0.4133 41.33%
Estrogen receptor binding + 0.7474 74.74%
Androgen receptor binding + 0.6888 68.88%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.7145 71.45%
Aromatase binding + 0.6995 69.95%
PPAR gamma + 0.6860 68.60%
Honey bee toxicity - 0.5799 57.99%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9895 98.95%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 97.12% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 96.73% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.38% 96.09%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 94.89% 96.77%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 92.81% 89.34%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 91.01% 91.07%
CHEMBL4040 P28482 MAP kinase ERK2 90.97% 83.82%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.68% 96.00%
CHEMBL340 P08684 Cytochrome P450 3A4 89.18% 91.19%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 88.75% 95.71%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.60% 94.45%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.07% 97.25%
CHEMBL299 P17252 Protein kinase C alpha 87.86% 98.03%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.98% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.90% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.77% 89.00%
CHEMBL2413 P32246 C-C chemokine receptor type 1 85.07% 89.50%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.87% 94.33%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.79% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.78% 99.23%
CHEMBL2996 Q05655 Protein kinase C delta 83.54% 97.79%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 83.46% 98.75%
CHEMBL3137262 O60341 LSD1/CoREST complex 82.40% 97.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.42% 86.33%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.87% 97.14%
CHEMBL5028 O14672 ADAM10 80.49% 97.50%

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.
Asplenium normale
Brucea javanica
Carpobrotus edulis
Castanea crenata
Centrolobium tomentosum
Ceratophyllum submersum
Dracocephalum kotschyi
Lippia carviodora
Myrica nana
Psilostrophe cooperi
Sideritis tragoriganum
Solanum jamaicense
Trifolium alexandrinum

Cross-Links

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PubChem 70686049
NPASS NPC146432
ChEMBL CHEMBL2037041