Bromomyrothenone B

Details

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Internal ID 464f7087-2bde-4eee-9067-c0517b879def
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Acyloins
IUPAC Name (5R)-3-amino-2-bromo-5-ethenyl-5-hydroxycyclopent-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H8BrNO2/c1-2-7(11)3-4(9)5(8)6(7)10/h2,11H,1,3,9H2/t7-/m0/s1
InChI Key TXDWSEOGINGPSP-ZETCQYMHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8BrNO2
Molecular Weight 218.05 g/mol
Exact Mass 216.97384 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.44
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Bromomyrothenone B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9821 98.21%
Caco-2 + 0.6606 66.06%
Blood Brain Barrier + 0.6750 67.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6471 64.71%
OATP2B1 inhibitior - 0.8628 86.28%
OATP1B1 inhibitior + 0.9609 96.09%
OATP1B3 inhibitior + 0.9425 94.25%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.8338 83.38%
BSEP inhibitior - 0.9029 90.29%
P-glycoprotein inhibitior - 0.9796 97.96%
P-glycoprotein substrate - 0.9805 98.05%
CYP3A4 substrate - 0.6621 66.21%
CYP2C9 substrate - 0.8065 80.65%
CYP2D6 substrate - 0.8237 82.37%
CYP3A4 inhibition - 0.7250 72.50%
CYP2C9 inhibition - 0.6802 68.02%
CYP2C19 inhibition - 0.6845 68.45%
CYP2D6 inhibition - 0.8645 86.45%
CYP1A2 inhibition - 0.7273 72.73%
CYP2C8 inhibition - 0.9660 96.60%
CYP inhibitory promiscuity - 0.7304 73.04%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7004 70.04%
Carcinogenicity (trinary) Non-required 0.4445 44.45%
Eye corrosion - 0.9615 96.15%
Eye irritation + 0.7717 77.17%
Skin irritation - 0.6938 69.38%
Skin corrosion - 0.8847 88.47%
Ames mutagenesis + 0.5600 56.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6779 67.79%
Micronuclear - 0.5268 52.68%
Hepatotoxicity + 0.6526 65.26%
skin sensitisation - 0.7104 71.04%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.6667 66.67%
Mitochondrial toxicity + 0.5875 58.75%
Nephrotoxicity + 0.7064 70.64%
Acute Oral Toxicity (c) III 0.6628 66.28%
Estrogen receptor binding - 0.9313 93.13%
Androgen receptor binding - 0.7125 71.25%
Thyroid receptor binding - 0.7243 72.43%
Glucocorticoid receptor binding - 0.8571 85.71%
Aromatase binding - 0.8814 88.14%
PPAR gamma - 0.7847 78.47%
Honey bee toxicity - 0.8372 83.72%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.5700 57.00%
Fish aquatic toxicity - 0.5812 58.12%

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 97.64% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.36% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.17% 95.56%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 82.37% 93.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.05% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.48% 89.34%
CHEMBL3137262 O60341 LSD1/CoREST complex 80.46% 97.09%

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 16109855
LOTUS LTS0183880
wikiData Q77496643