5 Results for "

CamA

" in MedChemExpress (MCE) Product Catalog:
Products (5)

5 Results for "CamA" in MCE Product Catalog:

Cat. No.: HY-148789
CAS No.: 2092925-89-6
Purity:  99.90%
Synonyms: OP-1250
Target:  

Estrogen Receptor/ERR

Research Areas:  

Inflammation/Immunology Cancer

Palazestrant is an antiestrogen and antineoplastic agent. Palazestrant can completely inhibit the activity of 17b-estradiol (E2) with IC50 value of 6.4 nM, and inhibit the proliferation of MCF7 and CAMA-1 cells with IC50 value of 1.4-1.6 nM. Palazestrant can inhibit ER +/HER2 + cancer .
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Cat. No.: HY-177046
CAS No.: 3092067-21-2
Research Areas:  

Cancer

KAT6A/KAT7-IN-4 is a KAT6A and KAT7 inhibitor. KAT6A/KAT7-IN-4 has IC50 values of both ≤ 1 nM for KAT6A and KAT7. KAT6A/KAT7-IN-4 can inhibit the acetylation of H3K14 and H3K23. KAT6A/KAT7-IN-4 also inhibits tumor cell proliferation, with an IC50 of ≤ 100 nM for CAMA-1. KAT6A/KAT7-IN-4 can be used in the study of breast cancer .
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Cat. No.: HY-148578
CAS No.: 2924055-46-7
Purity:  99.03%
Target:  

Bacterial

Research Areas:  

Infection

CamA-IN-1 is a Clostridioides difficile-specific DNA adenine methyltransferase (CamA) inhibitor. CamA-IN-1 has inhibitory for CamA with IC50 and Kd values of 0.4 μM and 0.2 μM, respectively. CamA-IN-1 can be used for the research of Clostridioides difficile infections (CDI) .
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Cat. No.: HY-168636
Research Areas:  

Cancer

p53 Activator 13 (compound 11) is a 6mA methyltransferase CamA inhibitor and a p53 activator. p53 Activator 13 intercalates into CamA-bound DNA via the minor groove, causing a conformational shift that moves the catalytic domain away from the DNA and elicits DNA damage response via p53 activation. p53 Activator 13 can be utilized in cancer research .
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Cat. No.: HY-170336
CAS No.: 2421260-43-5
Research Areas:  

Cancer

PROTAC ERα Degrader-10 is an orally active estrogen receptor α (ERα) PROTAC degrader, with DC50 values of 0.37, 1.1, and 0.47 nM in MCF7, T47D, and CAMA-1 cells, respectively. PROTAC ERα Degrader-10 exhibits significant anti-tumor activity both in vitro and in vivo, and can be used for breast cancer research .
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