Brevione I

Details

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Internal ID e09ebf1d-51bb-4db9-b468-95c73c9fca16
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name (2S,4'aS,4'bR,5'S,8'aR,10'aR)-5'-hydroxy-1',1',4'a,6,7,7',8'a-heptamethylspiro[3H-furo[3,2-c]pyran-2,8'-5,9,10,10a-tetrahydro-4bH-phenanthrene]-2',4-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C27H34O5/c1-14-12-18(28)22-25(6)10-9-20(29)24(4,5)19(25)8-11-26(22,7)27(14)13-17-21(32-27)15(2)16(3)31-23(17)30/h9-10,12,18-19,22,28H,8,11,13H2,1-7H3/t18-,19-,22+,25-,26+,27-/m0/s1
InChI Key AEGIBONSXCYUQG-OBSXHCQDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C27H34O5
Molecular Weight 438.60 g/mol
Exact Mass 438.24062418 g/mol
Topological Polar Surface Area (TPSA) 72.80 Ų
XlogP 3.60
Atomic LogP (AlogP) 4.46
H-Bond Acceptor 5
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Brevione I

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9862 98.62%
Caco-2 + 0.5679 56.79%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.8691 86.91%
OATP2B1 inhibitior - 0.8573 85.73%
OATP1B1 inhibitior + 0.8264 82.64%
OATP1B3 inhibitior + 0.8403 84.03%
MATE1 inhibitior - 0.8600 86.00%
OCT2 inhibitior - 0.5500 55.00%
BSEP inhibitior + 0.9645 96.45%
P-glycoprotein inhibitior + 0.7567 75.67%
P-glycoprotein substrate - 0.5782 57.82%
CYP3A4 substrate + 0.6939 69.39%
CYP2C9 substrate - 0.8151 81.51%
CYP2D6 substrate - 0.8649 86.49%
CYP3A4 inhibition - 0.6570 65.70%
CYP2C9 inhibition - 0.7113 71.13%
CYP2C19 inhibition - 0.7273 72.73%
CYP2D6 inhibition - 0.9083 90.83%
CYP1A2 inhibition + 0.6278 62.78%
CYP2C8 inhibition + 0.5000 50.00%
CYP inhibitory promiscuity - 0.8219 82.19%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.9600 96.00%
Carcinogenicity (trinary) Non-required 0.5020 50.20%
Eye corrosion - 0.9933 99.33%
Eye irritation - 0.9047 90.47%
Skin irritation - 0.5887 58.87%
Skin corrosion - 0.9003 90.03%
Ames mutagenesis - 0.7500 75.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6842 68.42%
Micronuclear - 0.7300 73.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation - 0.7827 78.27%
Respiratory toxicity + 0.5889 58.89%
Reproductive toxicity + 0.9222 92.22%
Mitochondrial toxicity + 0.8375 83.75%
Nephrotoxicity + 0.4519 45.19%
Acute Oral Toxicity (c) I 0.4237 42.37%
Estrogen receptor binding + 0.8666 86.66%
Androgen receptor binding + 0.7317 73.17%
Thyroid receptor binding + 0.7356 73.56%
Glucocorticoid receptor binding + 0.9008 90.08%
Aromatase binding + 0.8280 82.80%
PPAR gamma + 0.7696 76.96%
Honey bee toxicity - 0.8228 82.28%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity + 1.0000 100.00%

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 96.87% 91.11%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.30% 89.00%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.47% 100.00%
CHEMBL2581 P07339 Cathepsin D 87.24% 98.95%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.20% 97.09%
CHEMBL2850 P49840 Glycogen synthase kinase-3 alpha 85.26% 88.84%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 85.02% 95.56%
CHEMBL4829 O00763 Acetyl-CoA carboxylase 2 84.75% 98.00%
CHEMBL1871 P10275 Androgen Receptor 84.72% 96.43%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 83.98% 96.77%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 83.43% 93.04%
CHEMBL1293249 Q13887 Kruppel-like factor 5 83.40% 86.33%
CHEMBL1293277 O15118 Niemann-Pick C1 protein 81.05% 81.11%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.98% 94.00%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.94% 95.89%
CHEMBL253 P34972 Cannabinoid CB2 receptor 80.06% 97.25%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 139585980
LOTUS LTS0125509
wikiData Q77496166