Benazepril HCl - ≥99%, high purity , Angiotensin-converting enzyme inhibitor, CAS No.86541-74-4, Angiotensin-converting enzyme inhibitor

  • ≥99%
Item Number
B129257
Grouped product items
SKUSizeAvailabilityPrice Qty
B129257-250mg
250mg
In stock
$35.90
B129257-1g
1g
In stock
$117.90
B129257-5g
5g
In stock
$414.90
B129257-25g
25g
In stock
$1,867.90

Angiotensin-converting enzyme (ACE) inhibitor. Prodrug.

Basic Description

Synonyms2-[(3S)-3-{[(2S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino}-2-oxo-2,3,4,5-tetrahydro-1H-1-benzazepin-1-yl]acetic acid hydrochloride | 5NSA | Benazepril hydrochloride, European Pharmacopoeia (EP) Reference Standard | SR-01000762893-3 | HY-B0093A | NCGC000951
Specifications & Purity≥99%
Biochemical and Physiological MechanismsBenazepril hydrochloride is an ACE (angiotensin-converting enzyme) inhibitor. This prevents the catalytic conversion of angiotensin I to angiotensin II and in turn causes vasodilation and an increase in capillary blood volume.Angiotensin-converting enzyme
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
Action TypeINHIBITOR
Mechanism of actionAngiotensin-converting enzyme inhibitor
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

An angiotensin-converting enzyme (ACE) inhibitor

Associated Targets(Human)

POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TDP1 Tchem Tyrosyl-DNA phosphodiesterase 1 (345557 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CBX1 Tbio Chromobox protein homolog 1 (92434 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Galc Galactocerebrosidase (11 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Klebsiella pneumoniae (43867 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acinetobacter baumannii (41033 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cryptococcus neoformans (21258 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Names and Identifiers

IUPAC Name 2-[(3S)-3-[[(2S)-1-ethoxy-1-oxo-4-phenylbutan-2-yl]amino]-2-oxo-4,5-dihydro-3H-1-benzazepin-1-yl]acetic acid;hydrochloride
INCHI InChI=1S/C24H28N2O5.ClH/c1-2-31-24(30)20(14-12-17-8-4-3-5-9-17)25-19-15-13-18-10-6-7-11-21(18)26(23(19)29)16-22(27)28;/h3-11,19-20,25H,2,12-16H2,1H3,(H,27,28);1H/t19-,20-;/m0./s1
InChi Key VPSRQEHTHIMDQM-FKLPMGAJSA-N
Canonical SMILES CCOC(=O)C(CCC1=CC=CC=C1)NC2CCC3=CC=CC=C3N(C2=O)CC(=O)O.Cl
Isomeric SMILES CCOC(=O)[C@H](CCC1=CC=CC=C1)N[C@H]2CCC3=CC=CC=C3N(C2=O)CC(=O)O.Cl
WGK Germany 2
RTECS CX7065000
PubChem CID 5362123
Molecular Weight 460.95
Reaxy-Rn 4286047

Certificates

Certificate of Analysis(COA)

Enter Lot Number to search for COA:

Find and download the COA for your product by matching the lot number on the packaging.

6 results found

Lot NumberCertificate TypeDateItem
I2207440Certificate of AnalysisJun 05, 2024 B129257
I2207442Certificate of AnalysisJun 05, 2024 B129257
I2207443Certificate of AnalysisJun 05, 2024 B129257
K2110562Certificate of AnalysisAug 16, 2023 B129257
K2110564Certificate of AnalysisAug 16, 2023 B129257
H1503059Certificate of AnalysisMar 14, 2023 B129257

Chemical and Physical Properties

SolubilitySoluble in water (50 mM), DMSO (100 mM), ethanol, and methanol.
SensitivityMoisture sensitive.
Specific Rotation[α]-134.0 to -140.0 deg(C=1, EtOH)
Melt Point(°C)183°C(lit.)

Safety and Hazards(GHS)

Pictogram(s) GHS08
Signal Warning
Hazard Statements

H361:Suspected of damaging fertility or the unborn child

Precautionary Statements

P280:Wear protective gloves/protective clothing/eye protection/face protection.

P405:Store locked up.

P501:Dispose of contents/container to ...

P203:Obtain, read and follow all safety instructions before use.

P318:if exposed or concerned, get medical advice.

WGK Germany 2
RTECS CX7065000
Reaxy-Rn 4286047
Merck Index 1031

Related Documents

Citations of This Product

1. Wang Yiran, Shi Jihua, Dai Dapeng, Cai Jianping, Wang Shuanghu, Hong Yun, Zhou Shan, Zhao Fangling, Zhou Quan, Geng Peiwu, Zhou Yunfang, Xu Xue, Luo Qingfeng.  (2022)  Evaluation of commonly used cardiovascular drugs in inhibiting vonoprazan metabolism in vitro and in vivo.  Frontiers in Pharmacology,  13    [PMID:36052128] [10.3389/fphar.2022.909168]
2. Tan Lihua, Tu Yanbei, Wang Kai, Han Bing, Peng Hongquan, He Chengwei.  (2020)  Exploring protective effect of Glycine tabacina aqueous extract against nephrotic syndrome by network pharmacology and experimental verification.  Chinese Medicine,  15  (1): (1-17).  [PMID:32765640] [10.1186/s13020-020-00361-7]
3. Zheng Di-Wei, Pan Pei, Chen Ke-Wei, Fan Jin-Xuan, Li Chu-Xin, Cheng Han, Zhang Xian-Zheng.  (2020)  An orally delivered microbial cocktail for the removal of nitrogenous metabolic waste in animal models of kidney failure.  Nature Biomedical Engineering,  (9): (853-862).  [PMID:32632226] [10.1038/s41551-020-0582-1]

References

1. Wang Yiran, Shi Jihua, Dai Dapeng, Cai Jianping, Wang Shuanghu, Hong Yun, Zhou Shan, Zhao Fangling, Zhou Quan, Geng Peiwu, Zhou Yunfang, Xu Xue, Luo Qingfeng.  (2022)  Evaluation of commonly used cardiovascular drugs in inhibiting vonoprazan metabolism in vitro and in vivo.  Frontiers in Pharmacology,  13    [PMID:36052128] [10.3389/fphar.2022.909168]
2. Tan Lihua, Tu Yanbei, Wang Kai, Han Bing, Peng Hongquan, He Chengwei.  (2020)  Exploring protective effect of Glycine tabacina aqueous extract against nephrotic syndrome by network pharmacology and experimental verification.  Chinese Medicine,  15  (1): (1-17).  [PMID:32765640] [10.1186/s13020-020-00361-7]
3. Zheng Di-Wei, Pan Pei, Chen Ke-Wei, Fan Jin-Xuan, Li Chu-Xin, Cheng Han, Zhang Xian-Zheng.  (2020)  An orally delivered microbial cocktail for the removal of nitrogenous metabolic waste in animal models of kidney failure.  Nature Biomedical Engineering,  (9): (853-862).  [PMID:32632226] [10.1038/s41551-020-0582-1]

Solution Calculators