Briareolide G

Details

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Internal ID 77441a29-01a4-42a1-a3dc-4c67b6cbd46d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name [(1S,2R,7S,8Z,12R,13S,14S,16R,17R)-2,14-diacetyloxy-16-hydroxy-4,9,13,17-tetramethyl-5-oxo-6-oxatricyclo[11.4.0.03,7]heptadeca-3,8-dien-12-yl] butanoate
SMILES (Canonical) CCCC(=O)OC1CCC(=CC2C(=C(C(=O)O2)C)C(C3C1(C(CC(C3C)O)OC(=O)C)C)OC(=O)C)C
SMILES (Isomeric) CCCC(=O)O[C@@H]1CC/C(=C\[C@H]2C(=C(C(=O)O2)C)[C@@H]([C@@H]3[C@@]1([C@H](C[C@H]([C@@H]3C)O)OC(=O)C)C)OC(=O)C)/C
InChI InChI=1S/C28H40O9/c1-8-9-23(32)37-21-11-10-14(2)12-20-24(16(4)27(33)36-20)26(35-18(6)30)25-15(3)19(31)13-22(28(21,25)7)34-17(5)29/h12,15,19-22,25-26,31H,8-11,13H2,1-7H3/b14-12-/t15-,19+,20-,21+,22-,25+,26-,28-/m0/s1
InChI Key JBCNXCLMGJULMZ-PLUBAQGSSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C28H40O9
Molecular Weight 520.60 g/mol
Exact Mass 520.26723285 g/mol
Topological Polar Surface Area (TPSA) 125.00 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.57
H-Bond Acceptor 9
H-Bond Donor 1
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Briareolide G

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9955 99.55%
Caco-2 - 0.6285 62.85%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.6305 63.05%
OATP2B1 inhibitior - 0.8615 86.15%
OATP1B1 inhibitior + 0.8195 81.95%
OATP1B3 inhibitior + 0.9334 93.34%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.9572 95.72%
P-glycoprotein inhibitior + 0.8368 83.68%
P-glycoprotein substrate + 0.5830 58.30%
CYP3A4 substrate + 0.7076 70.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.9055 90.55%
CYP3A4 inhibition + 0.5810 58.10%
CYP2C9 inhibition - 0.8313 83.13%
CYP2C19 inhibition - 0.8860 88.60%
CYP2D6 inhibition - 0.9418 94.18%
CYP1A2 inhibition - 0.6937 69.37%
CYP2C8 inhibition + 0.5481 54.81%
CYP inhibitory promiscuity - 0.8815 88.15%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.5533 55.33%
Eye corrosion - 0.9871 98.71%
Eye irritation - 0.8972 89.72%
Skin irritation + 0.6725 67.25%
Skin corrosion - 0.8660 86.60%
Ames mutagenesis - 0.7564 75.64%
Human Ether-a-go-go-Related Gene inhibition - 0.5000 50.00%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.5355 53.55%
skin sensitisation - 0.7888 78.88%
Respiratory toxicity + 0.6556 65.56%
Reproductive toxicity + 0.7556 75.56%
Mitochondrial toxicity + 0.8750 87.50%
Nephrotoxicity - 0.5903 59.03%
Acute Oral Toxicity (c) III 0.5319 53.19%
Estrogen receptor binding + 0.8249 82.49%
Androgen receptor binding + 0.6529 65.29%
Thyroid receptor binding - 0.6036 60.36%
Glucocorticoid receptor binding + 0.7793 77.93%
Aromatase binding + 0.6069 60.69%
PPAR gamma + 0.7587 75.87%
Honey bee toxicity - 0.7403 74.03%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5068 50.68%
Fish aquatic toxicity + 0.9782 97.82%

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
CHEMBL230 P35354 Cyclooxygenase-2 98.08% 89.63%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 97.89% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 97.32% 96.09%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.34% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.85% 97.25%
CHEMBL1293249 Q13887 Kruppel-like factor 5 93.91% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 93.53% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 93.52% 99.23%
CHEMBL2581 P07339 Cathepsin D 93.32% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.96% 95.56%
CHEMBL3137262 O60341 LSD1/CoREST complex 91.55% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 91.01% 97.79%
CHEMBL221 P23219 Cyclooxygenase-1 87.81% 90.17%
CHEMBL2373 P21730 C5a anaphylatoxin chemotactic receptor 87.76% 92.62%
CHEMBL1994 P08235 Mineralocorticoid receptor 87.38% 100.00%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 86.94% 95.50%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 85.56% 94.80%
CHEMBL340 P08684 Cytochrome P450 3A4 83.49% 91.19%
CHEMBL241 Q14432 Phosphodiesterase 3A 82.81% 92.94%
CHEMBL5608 Q16288 NT-3 growth factor receptor 82.50% 95.89%
CHEMBL3060 Q9Y345 Glycine transporter 2 81.36% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.19% 94.45%

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.
There are no matching plants.

Cross-Links

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PubChem 23427830
LOTUS LTS0118004
wikiData Q105124235