B8011
DL-Benzylsuccinic acid
≥99%
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About This Item
Empirical Formula (Hill Notation):
C11H12O4
CAS Number:
Molecular Weight:
208.21
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
≥99%
Form:
powder
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)
InChI key
GTOFKXZQQDSVFH-UHFFFAOYSA-N
Gene Information
human ... CPA1(1357), CPB1(1360), CPM(1368), CPN1(1369)
wgk
WGK 3
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
Eyeshields, Gloves, type N95 (US)
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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 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
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
Global Trade Item Number
| SKU | GTIN |
|---|---|
| B8011-1G | 04061825594767 |
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