42 Results for "

CPI

" in MedChemExpress (MCE) Product Catalog:
Products (42)

42 Results for "CPI" in MCE Product Catalog:

26
26 Publications Verification
Cat. No.: HY-15453
CAS No.: 95809-78-2
Purity:  99.59%
Synonyms: CPI-613
Research Areas:  

Cancer

Devimistat is a mitochondrial metabolism inhibitor. Devimistat is a lipoic acid antagonist that abrogates mitochondrial energy metabolism to induce apoptosis in various cancer cells .
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14
14 Cited Publications
Cat. No.: HY-100421
CAS No.: 1628208-23-0
Purity:  98.31%
Target:  

Histone Demethylase

Research Areas:  

Cancer

CPI-455 is a specific, pan-KDM5 inhibitor with an IC50 of 10 nM for KDM5A. CPI-455 mediates KDM5 inhibition, elevates global levels of H3K4me3, and decreases the number of drug-tolerant persister cancer cells in multiple cancer cell line models treated with standard chemotherapy or targeted agents .
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14
14 Cited Publications
Cat. No.: HY-100421A
CAS No.: 2095432-28-1
Target:  

Histone Demethylase

Research Areas:  

Cancer

CPI-455 hydrochloride is a specific, pan-KDM5 inhibitor with an IC50 of 10 nM for KDM5A. CPI-455 hydrochloride mediates KDM5 inhibition, elevates global levels of H3K4me3, and decreases the number of drug-tolerant persister cancer cells in multiple cancer cell line models treated with standard chemotherapy or targeted agents .
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13
13 Cited Publications
Cat. No.: HY-100482
CAS No.: 1884712-47-3
Purity:  99.91%
CPI-637 is a selective and potent CBP/EP300 bromodomain inhibitor with IC50 values of 0.03 μM, 0.051 μM and 11.0 μM for CBP, EP300 and BRD4 BD-1, respectively, and an EC50 of 0.3 μM for CBP .
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9
9 Cited Publications
Cat. No.: HY-101978
CAS No.: 1202402-40-1
Purity:  99.85%
Synonyms: CPI-444; V81444
Target:  

Adenosine Receptor

Research Areas:  

Cancer

Ciforadenant (CPI-444) is a potent, orally active and selective adenosine A2A receptor (A2AR) antagonist, which induces antitumor responses .
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6
6 Cited Publications
Cat. No.: HY-15846
CAS No.: 1446144-04-2
Purity:  98.98%
Research Areas:  

Cancer

CPI-203 is a novel potent, selective and cell permeable inhibitor of BET bromodomain, with an IC50 value of appr 37 nM (BRD4 α-screen assay).
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3
3 Cited Publications
Cat. No.: HY-150298
CAS No.: 2226636-04-8
Purity:  99.71%
Synonyms: CPI-818
Target:  

Itk

Research Areas:  

Inflammation/Immunology Cancer

Soquelitinib (CPI-818) is an orally active and highly selective covalent interleukin-2-inducible kinase (ITK) inhibitor. Soquelitinib is active in six different models of T cell-mediated inflammatory and immune disease, including acute and chronic asthma, pulmonary fibrosis, systemic sclerosis (scleroderma), psoriasis, and acute graft versus host disease with Th2 cytokine product inhibition. Soquelitinib increases tumor infiltration of normal CD8 + cells that possess enhanced T effector function .
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Cat. No.: HY-12863
CAS No.: 1380087-89-7
Purity:  99.95%
Synonyms: CPI-0610
Research Areas:  

Cancer

Pelabresib (CPI-0610) is a potent, selective, orally active and cell-active BET inhibitor. Pelabresib inhibits BRD4-BD1 with an IC50 of 39 nM, and with an EC50 value of 0.18 μM for MYC .
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Cat. No.: HY-145602
CAS No.: 2567686-02-4
Purity:  98.75%
Synonyms: CPI-0209
Research Areas:  

Cancer

Tulmimetostat (CPI-0209) is an orally active EZH1/EZH2 inhibitor that targets and inhibits the EZH2 enzyme.Tulmimetostat has antitumor activity and is used in a variety of solid tumor studies .
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Cat. No.: HY-136285
CAS No.: 2374971-81-8
Purity:  99.74%
Research Areas:  

Cancer

CPI-1612 is a highly potent, orally active EP300/CBP histone acetyltransferase (HAT) inhibitor with an IC50 of 8.1 nM for EP300 HAT. CPI-1612 has an anticancer activity .
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Cat. No.: HY-P10856
CAS No.: 3085809-95-3
Target:  

P-glycoprotein

Research Areas:  

Cancer

CPI1 is a multidrug resistance protein 1 (MRP1) inhibitor with a Ki value of 100 nM. CPI1 binds to the same substrate-binding site as leukotriene C4, stabilizes MRP1 in an apo-like inward-facing conformation, blocks the conformational changes required for ATP hydrolysis and substrate transport, and inhibits the ATPase activity of human and bovine MRP1. CPI1 serves as a tool for investigating the substrate transport mechanism of MRP1. CPI1 is applicable to research related to cancer multidrug resistance .
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Cat. No.: HY-P99181
CAS No.: 2451856-97-4
Synonyms: CPI-006

Target:  

CD73

Mupadolimab (CPI-006) is an IgG1κ humanized FcγR binding-deficient anti-CD73 monoclonal antibody (mAb) that activates CD73 POS B cells .
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Cat. No.: HY-102024
CAS No.: 443103-97-7
Purity:  98.66%
Synonyms: CPI-444 analog
Target:  

Adenosine Receptor

Research Areas:  

Neurological Disease Cancer

A2A receptor antagonist 1 (CPI-444 analog) is an antagonist of both adenosine A2A receptor and A1 receptor with Ki values of 4 and 264 nM, respectively .
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Cat. No.: HY-42429
CAS No.: 1997304-12-7
CPI-203-PEG1-C3-O-COOH is a conjugate of the BRD4 ligand (HY-78695) and the linker (HY-42427). CPI-203-PEG1-C3-O-COOH can be used for synthesizing PROTAC BRD4 degrader ARV-771 (HY-100972) .
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Cat. No.: HY-123419
CAS No.: 1628214-07-2
Purity:  ≥99.0%
Target:  

Histone Demethylase

Research Areas:  

Cancer

CPI-4203 is a potent KDM5A inhibitor with an IC50 of 250 nM. CPI-4203 is competitive with 2-oxoglutarate (2-OG). CPI-4203 is structurally related to CPI-455 (HY-100421) but is less potent .
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Cat. No.: HY-100376
CAS No.: 183619-38-7
Purity:  98.49%
Target:  

TNF Receptor Apoptosis

Research Areas:  

Infection Neurological Disease

CPI-1189 is an orally active TNF-α release inhibitor. CPI-1189 inhibits phosphorylation of p38. CPI-1189 can inhibit apoptosis. CPI-1189 can be used in the study of HIV and neurological diseases .
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Cat. No.: HY-129379
CAS No.: 615538-51-7
Purity:  95.00%
Target:  

ADC Payloads

Research Areas:  

Cancer

DC0-NH2 is an effector moiety for ADC and a simplified analog of DC1 with better stability. DC0-NH2 is about 1000-fold more cytotoxic than commonly used anticancer agents (ex. Doxorubicin). DC0-NH2 can bind to the minor groove of DNA, followed by alkylation of adenine residues by its propabenzindole (CBI) component .
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Cat. No.: HY-P10759
CAS No.: 372491-73-1
Research Areas:  

Cancer

DTS-201 sodium (CPI-0004Na) is a peptidic prodrug of Doxorubicin (HY-15142A). DTS-201, comprising the tetrapeptide portion, is cleaved by endopeptidases in the tumor environment to produce metabolites that subsequently enter the cell and are converted to active Doxorubicin. DTS-201 shows antitumoral efficacy in tumor xenograft models of prostate, breast, and lung cancer .
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Cat. No.: HY-12863B
CAS No.: 1380089-81-5
CPI-0610 carboxylic acid is a ligand for target protein for PROTACT. CPI-0610 carboxylic acid is a potent bromodomain and extra-terminal (BET) protein inhibitor. CPI-0610 carboxylic acid has the potential in the therapy of multiple myeloma .
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Cat. No.: HY-134899
CAS No.: 2390367-27-6
Research Areas:  

Cancer

CPI-1328 is an EZH2 inhibitor with a Ki value of 63 fM.
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