Brevione E

Details

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Internal ID c0f1c55a-87e1-4c55-8852-b6060c63365b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbohydrates and carbohydrate conjugates > Monosaccharides
IUPAC Name [(1S,4R,10S,12R,13R,16R,21R,22R,23S)-3,6,7,17,22-pentamethyl-8,19-dioxo-5,11,24-trioxahexacyclo[19.2.1.04,10.04,13.013,23.016,22]tetracosa-2,6,17-trien-12-yl] acetate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C28H34O7/c1-13-9-18(30)11-22-26(6)19(13)7-8-27-24(26)21(33-22)10-14(2)28(27)23(34-25(27)32-17(5)29)12-20(31)15(3)16(4)35-28/h9-10,19,21-25H,7-8,11-12H2,1-6H3/t19-,21+,22-,23+,24+,25+,26+,27+,28+/m1/s1
InChI Key MPBWVNYITUYHFY-VKIAQROPSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C28H34O7
Molecular Weight 482.60 g/mol
Exact Mass 482.23045342 g/mol
Topological Polar Surface Area (TPSA) 88.10 Ų
XlogP 1.90
Atomic LogP (AlogP) 3.96
H-Bond Acceptor 7
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Brevione E

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9899 98.99%
Caco-2 - 0.5418 54.18%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7311 73.11%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8308 83.08%
OATP1B3 inhibitior + 0.8597 85.97%
MATE1 inhibitior - 0.6600 66.00%
OCT2 inhibitior - 0.6750 67.50%
BSEP inhibitior + 0.9257 92.57%
P-glycoprotein inhibitior + 0.8712 87.12%
P-glycoprotein substrate - 0.5164 51.64%
CYP3A4 substrate + 0.6996 69.96%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8820 88.20%
CYP3A4 inhibition - 0.7965 79.65%
CYP2C9 inhibition - 0.9178 91.78%
CYP2C19 inhibition - 0.8611 86.11%
CYP2D6 inhibition - 0.9518 95.18%
CYP1A2 inhibition - 0.6856 68.56%
CYP2C8 inhibition + 0.5124 51.24%
CYP inhibitory promiscuity - 0.8385 83.85%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9700 97.00%
Carcinogenicity (trinary) Non-required 0.4563 45.63%
Eye corrosion - 0.9853 98.53%
Eye irritation - 0.8872 88.72%
Skin irritation - 0.5587 55.87%
Skin corrosion - 0.8139 81.39%
Ames mutagenesis - 0.6864 68.64%
Human Ether-a-go-go-Related Gene inhibition + 0.7099 70.99%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.5166 51.66%
skin sensitisation - 0.7589 75.89%
Respiratory toxicity + 0.5333 53.33%
Reproductive toxicity + 0.8222 82.22%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity + 0.6260 62.60%
Acute Oral Toxicity (c) III 0.4648 46.48%
Estrogen receptor binding + 0.8600 86.00%
Androgen receptor binding + 0.7570 75.70%
Thyroid receptor binding + 0.5936 59.36%
Glucocorticoid receptor binding + 0.8554 85.54%
Aromatase binding + 0.6631 66.31%
PPAR gamma + 0.8104 81.04%
Honey bee toxicity - 0.7478 74.78%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.9748 97.48%

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 98.10% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.37% 96.09%
CHEMBL2581 P07339 Cathepsin D 92.96% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.82% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.25% 86.33%
CHEMBL1806 P11388 DNA topoisomerase II alpha 86.25% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 86.12% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 85.69% 93.04%
CHEMBL241 Q14432 Phosphodiesterase 3A 85.35% 92.94%
CHEMBL1994 P08235 Mineralocorticoid receptor 85.07% 100.00%
CHEMBL4026 P40763 Signal transducer and activator of transcription 3 84.35% 82.69%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 84.23% 97.14%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.20% 95.89%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.11% 94.80%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.77% 97.09%
CHEMBL340 P08684 Cytochrome P450 3A4 83.55% 91.19%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 83.34% 86.00%
CHEMBL4208 P20618 Proteasome component C5 83.01% 90.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 81.60% 85.14%
CHEMBL5255 O00206 Toll-like receptor 4 81.35% 92.50%
CHEMBL5028 O14672 ADAM10 80.72% 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.
There are no matching plants.

Cross-Links

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PubChem 139588445
LOTUS LTS0041954
wikiData Q105169317