43 Results for "

CPD self-cleavage

" in MedChemExpress (MCE) Product Catalog:
Products (43)

43 Results for "CPD self-cleavage" in MCE Product Catalog:

Cat. No.: HY-RS03089
Research Areas:  

Others

CPD Human Pre-designed siRNA Set A contains three designed siRNAs for CPD gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-168662
CAS No.: 2139329-57-8
Research Areas:  

Cancer

Palbociclib-CH2COOH is a Ligands for Target Protein for PROTACs. Palbociclib-CH2COOH can serve as an active control for the target protein ligand of CPD-39 (HY-168664) and CPD-10 (HY-168660) .
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Cat. No.: HY-144028
CAS No.: 2583778-77-0
Target:  

Trk Receptor

Research Areas:  

Cancer

Compound cpd-1 is a small molecule Trks inhibitor with good antitumor activity .
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Cat. No.: HY-158340
CAS No.: 2770471-05-9
Research Areas:  

Cancer

TYK2 ligand 1 is a TYK2 ligand in the synthesis of PROTAC-based TYK2 degrader (CPD-155, HY-158142) .
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Cat. No.: HY-168663
CAS No.: 3055814-59-7
Research Areas:  

Cancer

E3 Ligase Ligand-linker Conjugate 131 is a conjugate of E3 ligase ligand and linker that serve as a key intermediate for the synthesis of complete PROTAC molecule CPD-10 HY-168660 .
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Cat. No.: HY-168668
CAS No.: 3055816-67-3
Research Areas:  

Cancer

E3 Ligase Ligand-linker Conjugate 132 is a conjugate of E3 ligase ligand and linker that serve as a key intermediate for the synthesis of complete PROTAC molecule CPD-39 (HY-168664) .
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Cat. No.: HY-20240
CAS No.: 1239589-52-6
Target:  

PROTAC Linkers

Research Areas:  

Cancer

tert-Butyl (6-aminospiro[3.3]heptan-2-yl)carbamate is a linker that can be used for synthesis of PROTAC degrader CPD-39 (HY-168664) .
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Cat. No.: HY-134621
CAS No.: 2488868-36-4
Research Areas:  

Cancer

P300-IN-1 (cpd205) is a Histone acetylase p300 inhibitor .
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Cat. No.: HY-153441
CAS No.: 1954722-22-5
Target:  

TAM Receptor

Research Areas:  

Cancer

AXL-IN-15 (cpd391) is a potent Axl inhibitor with both Ki and IC50 <1 nM. AXL-IN-15 can be used for research in cancer .
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Cat. No.: HY-P4914
CAS No.: 120116-56-5
Target:  

Sex Pheromone

Research Areas:  

Others

Sex Pheromone Inhibitor iPD1 is a sex pheromone inhibitor. Sex Pheromone Inhibitor iPD1 inhibits the sex pheromone cPD1 .
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Cat. No.: HY-P4523
CAS No.: 76079-06-6
Target:  

Endogenous Metabolite

Research Areas:  

Endocrinology

FA-Ala-Arg is a dipeptide with furylacryloyl group. FA-Ala-Arg breaks down to produce arginine. While cell-surface Carboxypeptidase-D (CPD) also increases intracellular Arg, which is converted to nitric oxide (NO). FA-Ala-Arg enhances NO production in MCF-7 cells. FA-Ala-Arg also increases the cell survival of prolactin (PRL)-treated cells, PRL regulates CPD mRNA levels in cells .
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Cat. No.: HY-W585819R
CAS No.: 51930-97-3
Synonyms: 3-MPCD dipalmitate (Standard); 3-CPD dipalmitate (Standard)
Research Areas:  

Others

3-Chloropropane-1,2-diol dipalmitate (3-MPCD dipalmitate) Standard is the analytical standard of 3-Chloropropane-1,2-diol dipalmitate (HY-W585819). This product is intended for research and analytical applications. 3-Chloropropane-1,2-diol dipalmitate (3-MPCD dipalmitate) is a fatty acid ester of 3-monochloropropane-1,2-diol (3-MCPD) and a foodborne contaminant .
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Cat. No.: HY-W471937
CAS No.: 874129-03-0
α1b-AR antagonist 1 (Compound Cpd1) is a selective α1B-AR antagonist. Alpha1b-ar antagonist 1 can be used in the study of cardiovascular and central nervous system diseases .
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Cat. No.: HY-179364
CAS No.: 1224565-08-5
Target:  

Apolipoprotein

Research Areas:  

Metabolic Disease

PLTP-IN-1 (cpd B) is a selective phospholipid transfer protein (PLTP) inhibitor with an IC50 of 1.6 μM. PLTP-IN-1 can block the phospholipid transfer mediated by PLTP and reduce the secretion of apolipoprotein B. PLTP-IN-1 has no effect on the level of triglycerides. PLTP-IN-1 can be used for the research of metabolic disease, such as hyperlipidemia .
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Cat. No.: HY-W585819S
CAS No.: 3044743-84-9
Synonyms: 3-MPCD dipalmitate-13C3; 3-CPD dipalmitate-13C3
3-Chloropropane-1,2-diol dipalmitate- 13C3 (3-MPCD dipalmitate- 13C3) is 13C labeled 3-Chloropropane-1,2-diol dipalmitate (HY-W585819). 3-Chloropropane-1,2-diol dipalmitate (3-MPCD dipalmitate) is a fatty acid ester of 3-monochloropropane-1,2-diol (3-MCPD) and a foodborne contaminant .
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Cat. No.: HY-178488
CAS No.: 2468048-19-1
Target:  

SWI/SNF Complex

Research Areas:  

Infection Cancer

BRM/BRG1 ATP-IN-7 (Compound Cpd69) is a selective dual BRM (SMARCA2) and BRG1 (SMARCA4) inhibitor with IC50 values of 12 nM and 8 nM, respectively. BRM/BRG1 ATP-IN-7 is promising for research of BRM/BRG1-dependent cancers (e.g., non-small cell lung cancer, Ewing sarcoma) and virus-associated diseases (e.g., HPV infection) .
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Cat. No.: HY-172455
CAS No.: 3023854-95-4
Target:  

Potassium Channel

Research Areas:  

Neurological Disease

TREK inhibitor-3 (Cpd8l) is a selective and BBB-permeable TREK-1 inhibitor with an IC50 of 0.81 μM. TREK inhibitor-3 has neuroprotective effects, which can significantly reduce the death of cortical neurons induced by oxygen-glucose deprivation/reoxygenation (OGD/R) and improve brain injury in mice models of middle cerebral artery occlusion/reperfusion (MCAO/R). TREK inhibitor-3 can be used in the research of ischemic stroke .
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Cat. No.: HY-178490
CAS No.: 2468046-72-0
Target:  

SWI/SNF Complex

Research Areas:  

Cancer

BRM/BRG1 ATP-IN-8 (Compound Cpd14) is an orally active BRG1/BRM ATPase domain inhibitor. BRM/BRG1 ATP-IN-8 exerts antitumor effects by disrupting aberrant chromatin remodeling in cancer cells, inducing apoptosis and growth arrest. BRM/BRG1 ATP-IN-8 is promising for research of BRG1/BRM-dependent malignancies, including hematological cancers, prostate cancer, breast cancer, and Ewing's sarcoma .
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Cat. No.: HY-169059
Target:  

Ferroptosis

Research Areas:  

Inflammation/Immunology

Ferroptosis-IN-12 (Cpd-A1) is a ferroptosis inhibitor. Ferroptosis-IN-12 exhibits effective ferroptosis inhibition in Erastin (HY-15763)-treated mouse tubular epithelial cells (mTECs) and improves kidney function, alleviates renal tubular damage, and reduces inflammation in a dose-dependent manner in acute kidney injury (AKI) mouse models induced by ischemia/reperfusion (I/R) or cecal ligation and puncture (CLP). Ferroptosis-IN-12 demonstrates good plasma stability and high distribution in kidney tissues in pharmacokinetic studies in mice. Ferroptosis-IN-12 holds promise for research in the field of acute kidney injury (AKI) .
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Cat. No.: HY-RS18891
Research Areas:  

Others

Cpd Mouse Pre-designed siRNA Set A contains three designed siRNAs for Cpd gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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