Myrothenone B

Details

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Internal ID 5ebe0329-0179-4cf8-9da6-d35c9fb310e4
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Acyloins
IUPAC Name (5R)-3-amino-5-ethenyl-5-hydroxycyclopent-2-en-1-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H9NO2/c1-2-7(10)4-5(8)3-6(7)9/h2-3,10H,1,4,8H2/t7-/m0/s1
InChI Key RNZVUWAMBDXWDJ-ZETCQYMHSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C7H9NO2
Molecular Weight 139.15 g/mol
Exact Mass 139.063328530 g/mol
Topological Polar Surface Area (TPSA) 63.30 Ų
XlogP -0.30
Atomic LogP (AlogP) -0.28
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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AKOS006348244
(5R)-3-amino-5-ethenyl-5-hydroxycyclopent-2-en-1-one

2D Structure

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2D Structure of Myrothenone B

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9836 98.36%
Caco-2 + 0.8115 81.15%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.6450 64.50%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9615 96.15%
OATP1B3 inhibitior + 0.9446 94.46%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9088 90.88%
BSEP inhibitior - 0.9339 93.39%
P-glycoprotein inhibitior - 0.9841 98.41%
P-glycoprotein substrate - 0.9610 96.10%
CYP3A4 substrate - 0.6630 66.30%
CYP2C9 substrate - 0.8071 80.71%
CYP2D6 substrate - 0.8202 82.02%
CYP3A4 inhibition - 0.8803 88.03%
CYP2C9 inhibition - 0.8489 84.89%
CYP2C19 inhibition - 0.7600 76.00%
CYP2D6 inhibition - 0.9232 92.32%
CYP1A2 inhibition - 0.8269 82.69%
CYP2C8 inhibition - 0.9854 98.54%
CYP inhibitory promiscuity - 0.8669 86.69%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.7600 76.00%
Carcinogenicity (trinary) Non-required 0.5358 53.58%
Eye corrosion - 0.9621 96.21%
Eye irritation + 0.9519 95.19%
Skin irritation - 0.6646 66.46%
Skin corrosion - 0.8496 84.96%
Ames mutagenesis + 0.5463 54.63%
Human Ether-a-go-go-Related Gene inhibition - 0.8189 81.89%
Micronuclear + 0.5232 52.32%
Hepatotoxicity + 0.5847 58.47%
skin sensitisation - 0.6833 68.33%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5740 57.40%
Acute Oral Toxicity (c) III 0.6525 65.25%
Estrogen receptor binding - 0.9348 93.48%
Androgen receptor binding - 0.5345 53.45%
Thyroid receptor binding - 0.7847 78.47%
Glucocorticoid receptor binding - 0.8686 86.86%
Aromatase binding - 0.8682 86.82%
PPAR gamma - 0.8583 85.83%
Honey bee toxicity - 0.8211 82.11%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.5600 56.00%
Fish aquatic toxicity - 0.8619 86.19%

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 98.18% 91.11%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 91.35% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.89% 95.56%
CHEMBL4208 P20618 Proteasome component C5 80.33% 90.00%

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 11298006
LOTUS LTS0089427
wikiData Q105241977