B8011
DL-Benzylsuccinic acid
≥99%
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About This Item
Empirical Formula (Hill Notation):
C11H12O4
CAS Number:
Molecular Weight:
208.21
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
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)
InChI key
GTOFKXZQQDSVFH-UHFFFAOYSA-N
Gene Information
human ... CPA1(1357), CPB1(1360), CPM(1368), CPN1(1369)
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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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 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.
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
History of heart failure.
Hector O Ventura
Congestive heart failure (Greenwich, Conn.), 15(1), 49-49 (2009-02-04)
D R Abendschein et al.
The Journal of laboratory and clinical medicine, 110(6), 798-806 (1987-12-01)
This study was undertaken to identify the carboxypeptidase(s) (CPase) in plasma mediating sequential conversion of the tissue isoform of the MM isoenzyme of creatine kinase (MM3 CK) to MM2 and MM1 isoforms and to elucidate relationships between CPase activity measured
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