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Dokumente

B8011

Sigma-Aldrich

DL-Benzylbernsteinsäure

≥99%

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About This Item

Empirische Formel (Hill-System):
C11H12O4
CAS-Nummer:
884-33-3
Molekulargewicht:
208.21
MDL-Nummer:
MFCD00055798
UNSPSC-Code:
12352100
PubChem Substanz-ID:
24892039
NACRES:
NA.22

Assay

≥99%

Form

powder

SMILES String

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)

InChIKey

GTOFKXZQQDSVFH-UHFFFAOYSA-N

Angaben zum Gen

human ... CPA1(1357) , CPB1(1360) , CPM(1368) , CPN1(1369)

Lagerklassenschlüssel

11 - Combustible Solids

WGK

WGK 3

Flammpunkt (°F)

Not applicable

Flammpunkt (°C)

Not applicable

Persönliche Schutzausrüstung

Eyeshields, Gloves, type N95 (US)

Analysenzertifikate (COA)

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A Gumà et al.
Molecular and cellular endocrinology, 91(1-2), 29-33 (1993-02-01)
Benzyl succinate inhibited insulin binding and tyrosine receptor kinase in a concentration-dependent manner in the partially purified insulin receptor preparation from rat skeletal muscle. Benzyl succinate lowered the apparent number of high-affinity insulin binding sites. We have made use of
D W Cushman et al.
The American journal of cardiology, 49(6), 1390-1394 (1982-04-21)
Captopril is a remarkably effective new antihypertensive drug designed and developed as a potent and specific inhibitor of angiotensin-converting enzyme, a zinc metallopeptidase that participates in the synthesis of a hypertensive peptide, angiotensin II, and in the degradation of a
A C Hausrath et al.
The Journal of biological chemistry, 269(29), 18839-18842 (1994-07-22)
The complex of benzylsuccinic acid with thermolysin has been redetermined at 1.7-A resolution and refined to a crystallographic residual of 15.7%. In contrast to the prior study, which was to 2.3-A resolution, and without the benefit of refinement (Bolognesi, M.
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
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
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