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A0773

Angiotensin Converting Enzyme Inhibitor

≥95% (TLC)

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5 MG

€131.75

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About This Item

Empirical Formula (Hill Notation):
C53H76N14O12
CAS Number:
35115-60-7
Molecular Weight:
1101.26
NACRES:
NA.77
PubChem Substance ID:
329770629
UNSPSC Code:
12352200
MDL number:
MFCD00076208

Key Documents

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Product Name

Angiotensin Converting Enzyme Inhibitor, ≥95% (TLC)

InChI key

UUUHXMGGBIUAPW-CSCXCSGISA-N

SMILES string

CC[C@H](C)[C@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H]1CCCN1C(=O)[C@H](CCCNC(N)=N)NC(=O)[C@@H]2CCCN2C(=O)[C@H](Cc3c[nH]c4ccccc34)NC(=O)[C@@H]5CCC(=O)N5)C(=O)N6CCC[C@H]6C(=O)N7CCC[C@H]7C(O)=O

InChI

1S/C53H76N14O12/c1-3-29(2)43(51(77)66-25-9-16-39(66)50(76)67-26-10-17-40(67)52(78)79)63-45(71)34(18-20-41(54)68)60-46(72)37-14-7-23-64(37)48(74)35(13-6-22-57-53(55)56)61-47(73)38-15-8-24-65(38)49(75)36(62-44(70)33-19-21-42(69)59-33)27-30-28-58-32-12-5-4-11-31(30)32/h4-5,11-12,28-29,33-40,43,58H,3,6-10,13-27H2,1-2H3,(H2,54,68)(H,59,69)(H,60,72)(H,61,73)(H,62,70)(H,63,71)(H,78,79)(H4,55,56,57)/t29-,33-,34-,35-,36-,37-,38-,39-,40-,43-/m0/s1

biological source

synthetic (organic)

assay

≥95% (TLC)

form

powder

mol wt

~_1.1 kDa

solubility

water: soluble 1 mg/mL, clear, colorless

storage temp.

−20°C

Quality Level

200

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1 of 4

This Item
A6185A0230P7340
Angiotensin Converting Enzyme Inhibitor ≥95% (TLC)

Sigma-Aldrich

A0773

Angiotensin Converting Enzyme Inhibitor

Calpain Inhibitor I ≥97% (TLC), powder

Sigma-Aldrich

A6185

Calpain Inhibitor I

Angiotensin IV trifluoroacetate salt ≥95% (HPLC), powder

Sigma-Aldrich

A0230

Angiotensin IV trifluoroacetate salt

(±)-threo-1-Phenyl-2-decanoylamino-3-morpholino-1-propanol hydrochloride

Sigma-Aldrich

P7340

(±)-threo-1-Phenyl-2-decanoylamino-3-morpholino-1-propanol hydrochloride

form

powder

form

powder

form

powder

form

powder

assay

≥95% (TLC)

assay

≥97% (TLC)

assay

≥95% (HPLC)

assay

≥98% (TLC)

Quality Level

200

Quality Level

200

Quality Level

100

Quality Level

100

mol wt

~_1.1 kDa

mol wt

-

mol wt

-

mol wt

-

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

solubility

water: soluble 1 mg/mL, clear, colorless

solubility

DMSO: soluble, ethanol: soluble

solubility

H2O: ~1 mg/mL

solubility

water: 50 mg/mL, clear, colorless

Storage Class

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
0000496363
0000496363
SLCH1799
0000461906
0000456411

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Of mice and men: therapeutic mTOR inhibition in polycystic kidney disease.
York Pei
Journal of the American Society of Nephrology : JASN, 21(3), 390-391 (2010-02-06)
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Bioorganic & medicinal chemistry, 18(9), 3320-3334 (2010-03-30)
Novel alpha-mannosidase inhibitors of the type (2R,3R,4S)-2-({[(1R)-2-hydroxy-1-arylethyl]amino}methyl)pyrrolidine-3,4-diol have been prepared and assayed for their anticancer activities. Compound 30 with the aryl group=4-trifluoromethylbiphenyl inhibits the proliferation of primary cells and cell lines of different origins, irrespective of Bcl-2 expression levels, inducing
Oscar Gallardo et al.
The Journal of biological chemistry, 285(4), 2721-2733 (2009-11-27)
Paenibacillus barcinonensis is a soil bacterium bearing a complex set of enzymes for xylan degradation, including several secreted enzymes and Xyn10B, one of the few intracellular xylanases reported to date. The crystal structure of Xyn10B has been determined by x-ray
R Matsas et al.
The Biochemical journal, 223(2), 433-440 (1984-10-15)
Endopeptidase-24.11 (EC 3.4.24.11), purified to homogeneity from pig kidney, was shown to hydrolyse a wide range of neuropeptides, including enkephalins, tachykinins, bradykinin, neurotensin, luliberin and cholecystokinin. The sites of hydrolysis of peptides were identified, indicating that the primary specificity is
Meden F Isaac-Lam
In silico pharmacology, 9(1), 55-55 (2021-10-12)
COVID-19 is a new communicable disease with a widespread outbreak that affects all populations worldwide triggering a rush of scientific interest in coronavirus research globally. In silico molecular docking experiment was utilized to determine interactions of available compounds with SARS-CoV-2
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