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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
Recommended Products
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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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.
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 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
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