B8011
DL-Benzylsuccinic acid
≥99%
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About This Item
Formule empirique (notation de Hill):
C11H12O4
Numéro CAS:
Poids moléculaire :
208.21
Numéro MDL:
Code UNSPSC :
12352100
ID de substance PubChem :
Nomenclature NACRES :
NA.22
Produits recommandés
Essai
≥99%
Forme
powder
Chaîne SMILES
OC(=O)CC(Cc1ccccc1)C(O)=O
InChI
1S/C11H12O4/c12-10(13)7-9(11(14)15)6-8-4-2-1-3-5-8/h1-5,9H,6-7H2,(H,12,13)(H,14,15)
Clé InChI
GTOFKXZQQDSVFH-UHFFFAOYSA-N
Informations sur le gène
human ... CPA1(1357) , CPB1(1360) , CPM(1368) , CPN1(1369)
Code de la classe de stockage
11 - Combustible Solids
Classe de danger pour l'eau (WGK)
WGK 3
Point d'éclair (°F)
Not applicable
Point d'éclair (°C)
Not applicable
Équipement de protection individuelle
Eyeshields, Gloves, type N95 (US)
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H R Beller et al.
Applied and environmental microbiology, 58(9), 3192-3195 (1992-09-01)
Two dead-end metabolites of anaerobic toluene transformation, benzylsuccinic acid and benzylfumaric acid, accumulated in sulfate-reducing enrichment cultures that were fed toluene as the sole carbon source. Stable isotope-labeled toluene and gas chromatography-mass spectrometry were used to confirm that the compounds
D E Reusser et al.
Journal of chromatography. A, 953(1-2), 215-225 (2002-06-13)
Benzylsuccinic acid (BSA) and methylbenzylsuccinic acid (methyl-BSA) are unambiguous biotransformation products resulting from anaerobic toluene and xylene biodegradation, respectively. A solid-phase extraction method based on polystyrene-divinylbenzene sorbent was developed for the quantitative BSA determination in groundwater samples as an alternative
S Mangani et al.
Journal of molecular biology, 223(2), 573-578 (1992-01-20)
The X-ray crystal structure of the carboxypeptidase A-L-benzylsuccinate complex has been refined at 2.0 A resolution to a final R-factor of 0.166. One molecule of the inhibitor binds to the enzyme active site. The terminal carboxylate forms a salt link
D R Webster et al.
Journal of cellular biochemistry, 60(3), 424-436 (1996-03-01)
alpha-tubulin subunits within microtubules (MTs) can be post-translationally detyrosinated by a tubulin-specific carboxypeptidase (TCP) activity to form biochemically distinct MTs. Attempts to characterize and purify TCP have suffered from the inability to detect low levels of activity and to distinguish
Ya-lou Wang et al.
Yao xue xue bao = Acta pharmaceutica Sinica, 44(5), 491-495 (2009-07-22)
Based on the SAR of glinide agents, mitiglinide has been modified to study the SAR of glinides. a-Benzylsuccinic acid derivatives which were designed and synthesized in order to find some more hypoglycemic active agents and further investigate the SAR of
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