Ac-LEHD-AMC

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Ac-LEHD-AMC

Ac-LEHD-AMC | 292633-16-0

Catalog Number A18-0023
Category Fluorescent Enzyme Substrates
Molecular Formula C33H41N7O11
Molecular Weight 711.7
Catalog Number Size Price Quantity
A18-0023 -- $--

Product Introduction

Ac-LEHD-AMC is a fluorogenic substrate for caspase-9. Ac-LEHD-AMC is cleaved by caspase-9 to release the fluorescent moiety AMC, which can be used to quantify caspase-9 activity.

Chemical Information

Synonyms N-acetyl-L-leucyl-L-α-glutamyl-L-histidyl-N-(4-methyl-2-oxo-2H-1-benzopyran-7-yl)-L-α-asparagine
Purity ≥95%
IUPAC Name (4S)-4-[[(2S)-2-acetamido-4-methylpentanoyl]amino]-5-[[(2S)-1-[[(2S)-3-carboxy-1-[(4-methyl-2-oxochromen-7-yl)amino]-1-oxopropan-2-yl]amino]-3-(1H-imidazol-5-yl)-1-oxopropan-2-yl]amino]-5-oxopentanoic acid
Canonical SMILES CC1=CC(=O)OC2=C1C=CC(=C2)NC(=O)C(CC(=O)O)NC(=O)C(CC3=CN=CN3)NC(=O)C(CCC(=O)O)NC(=O)C(CC(C)C)NC(=O)C
InChI InChI=1S/C33H41N7O11.C2HF3O2/c1-16(2)9-23(36-18(4)41)32(49)38-22(7-8-27(42)43)30(47)39-24(11-20-14-34-15-35-20)33(50)40-25(13-28(44)45)31(48)37-19-5-6-21-17(3)10-29(46)51-26(21)12-19;3-2(4,5)1(6)7/h5-6,10,12,14-16,22-25H,7-9,11,13H2,1-4H3,(H,34,35)(H,36,41)(H,37,48)(H,38,49)(H,39,47)(H,40,50)(H,42,43)(H,44,45);(H,6,7)/t22-,23-,24-,25-;/m0./s1
InChI Key UOZNIAKIZDCQSH-NATPOTRJSA-N
  • Product Specification
  • Application
Storage Store at -20°C

Ac-LEHD-AMC, a synthetic peptide substrate utilized in biochemical research, serves various purposes in scientific exploration. Here are four key applications of Ac-LEHD-AMC:

Caspase Activity Assays: A cornerstone in the realm of apoptotic pathways, Ac-LEHD-AMC is a pivotal tool for assessing caspase-9 activity. Upon cleavage by the active caspase-9, this substrate liberates a fluorescent AMC molecule, offering a measurable signal. This assay plays a critical role in delving into programmed cell death intricacies and screening potential drugs that modulate apoptosis.

Drug Screening: In the domain of pharmaceutical research, Ac-LEHD-AMC serves as a linchpin in the identification and evaluation of caspase-9 inhibitors. High-throughput screening assays leveraging this substrate can swiftly gauge the effectiveness of novel drug candidates. This contributes significantly to uncovering innovative therapeutic agents tailored to combat apoptosis-related afflictions like cancer.

Biomedical Research: Ac-LEHD-AMC is a prized asset for researchers aiming to unravel the involvement of caspase-9 in diverse diseases ranging from neurodegenerative disorders to cardiovascular conditions. By monitoring caspase activity, scientists delve into disease mechanisms and the impact of apoptosis on disease progression. This knowledge forms the bedrock for crafting precision interventions targeted at specific ailments.

Pathway Elucidation: A key ally in unraveling apoptosis pathways, Ac-LEHD-AMC facilitates precise measurement of caspase-9 activity within cellular milieus. By employing this substrate, researchers can track real-time fluctuations in caspase activity across varied experimental settings. This aids in deciphering the intricate web of signaling pathways governing cell survival and demise, shedding light on the mysteries of life processes.

Computed Properties

XLogP3 -0.3
Hydrogen Bond Donor Count 8
Hydrogen Bond Acceptor Count 12
Rotatable Bond Count 18
Exact Mass 711.28640515 g/mol
Monoisotopic Mass 711.28640515 g/mol
Topological Polar Surface Area 275Ų
Heavy Atom Count 51
Formal Charge 0
Complexity 1370
Isotope Atom Count 0
Defined Atom Stereocenter Count 4
Undefined Atom Stereocenter Count 0
Defined Bond Stereocenter Count 0
Undefined Bond Stereocenter Count 0
Covalently-Bonded Unit Count 1
Compound Is Canonicalized Yes

Patents

Publication NumberTitlePriority Date
EP-3929209-A1 Vasopressin-2 receptor antagonist peptides and uses thereof 2020-06-24
WO-2019227240-A1 Methods for treating cancer with acyldepsipeptide analogs 2018-06-01
CA-3102215-A1 Methods for treating cancer with acyldepsipeptide analogs 2018-06-01
US-2021122780-A1 Compositions for the prevention and treatment of parkinson's disease 2018-03-29
US-2022267367-A1 Compositions for the prevention and treatment of parkinson's disease 2018-03-29
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