(2R,3E,5R)-3-(2-Hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo(3.2.0)heptane-2-carboxylic acid

Details

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Internal ID 7ca8fcdb-3b43-4d95-a18f-58b6074211cc
Taxonomy Organic acids and derivatives > Carboxylic acids and derivatives > Amino acids, peptides, and analogues > Alpha amino acids and derivatives
IUPAC Name (2R,3E,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H9NO5/c10-2-1-4-7(8(12)13)9-5(11)3-6(9)14-4/h1,6-7,10H,2-3H2,(H,12,13)/b4-1+/t6-,7-/m1/s1
InChI Key HZZVJAQRINQKSD-INJCQMSSSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C8H9NO5
Molecular Weight 199.16 g/mol
Exact Mass 199.04807239 g/mol
Topological Polar Surface Area (TPSA) 87.10 Ų
XlogP -1.20
Atomic LogP (AlogP) -1.10
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 2

Synonyms

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62319-53-3
C11833
(2R,3E,5R)-3-(2-hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo[3.2.0]heptane-2-carboxylic acid
58001-44-8
AC1NQXVM
SureCN2292022
SCHEMBL2292022
CHEBI:29607
CHEBI:94565
DTXSID001121437
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (2R,3E,5R)-3-(2-Hydroxyethylidene)-7-oxo-4-oxa-1-azabicyclo(3.2.0)heptane-2-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9685 96.85%
Caco-2 - 0.8016 80.16%
Blood Brain Barrier - 0.6750 67.50%
Human oral bioavailability + 0.8571 85.71%
Subcellular localzation Mitochondria 0.5321 53.21%
OATP2B1 inhibitior - 0.8612 86.12%
OATP1B1 inhibitior + 0.9450 94.50%
OATP1B3 inhibitior + 0.9382 93.82%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.9601 96.01%
P-glycoprotein inhibitior - 0.9805 98.05%
P-glycoprotein substrate - 0.9426 94.26%
CYP3A4 substrate - 0.5859 58.59%
CYP2C9 substrate - 0.7962 79.62%
CYP2D6 substrate - 0.8367 83.67%
CYP3A4 inhibition - 0.9798 97.98%
CYP2C9 inhibition - 0.8957 89.57%
CYP2C19 inhibition - 0.8915 89.15%
CYP2D6 inhibition - 0.9295 92.95%
CYP1A2 inhibition - 0.8694 86.94%
CYP2C8 inhibition - 0.9695 96.95%
CYP inhibitory promiscuity - 0.9926 99.26%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.8700 87.00%
Carcinogenicity (trinary) Non-required 0.5265 52.65%
Eye corrosion - 0.9743 97.43%
Eye irritation + 0.6097 60.97%
Skin irritation - 0.7319 73.19%
Skin corrosion - 0.9107 91.07%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8735 87.35%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.5678 56.78%
skin sensitisation - 0.9436 94.36%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity - 0.6314 63.14%
Acute Oral Toxicity (c) IV 0.6106 61.06%
Estrogen receptor binding - 0.8399 83.99%
Androgen receptor binding - 0.4885 48.85%
Thyroid receptor binding - 0.7379 73.79%
Glucocorticoid receptor binding - 0.6685 66.85%
Aromatase binding - 0.8955 89.55%
PPAR gamma - 0.4928 49.28%
Honey bee toxicity - 0.9313 93.13%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.7900 79.00%
Fish aquatic toxicity - 0.8223 82.23%

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
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.98% 85.14%
CHEMBL3807 P17706 T-cell protein-tyrosine phosphatase 85.54% 93.00%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.15% 95.56%
CHEMBL340 P08684 Cytochrome P450 3A4 82.67% 91.19%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.65% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.39% 96.09%

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 5281002
LOTUS LTS0027179
wikiData Q27110175