21 Results for "

BCC

" in MedChemExpress (MCE) Product Catalog:
Products (21)

21 Results for "BCC" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-113965
CAS No.: 334998-36-6
Purity:  99.04%
Target:  

Hedgehog Smo Apoptosis

Research Areas:  

Inflammation/Immunology

CUR61414 is a novel, potent and cell permeable Hedgehog signaling pathway inhibitor (IC50 =100-200 nM). CUR61414 is a small-molecule aminoproline class compound and selectively binds to smoothened (Smo) with a Ki value of 44 nM. CUR-61414 can induce apoptosis in cancer cells without affecting neighboring non-tumor cells .
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1
1 Cited Publications
Cat. No.: HY-P72257
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: BCC7; p53; p53 tumor suppressor; Phosphoprotein p5
Species:  
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Cat. No.: HY-NP131
Recombinant Humanized Type III Collagen 10.4kDa is a novel biomaterial that have anticancer effects. Recombinant Humanized Type III Collagen 10.4kDa activates discoidin domain receptor 1 (DDR1), and thus inhibits autophagy, proliferation, and migration of cancer cells, and induces apoptosis .
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Cat. No.: HY-126202
CAS No.: 903892-99-9
Lachnone A is a chromone derivative isolated from the filamentous fungus Lachnum sp. BCC 2424 .
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Cat. No.: HY-124301
CAS No.: 1418291-68-5
Penicolinate A is a picolinic acid derivative. Penicolinate A is isolated from endophytic Penicillium sp. BCC16054. Penicolinate A exhibits antimalarial and antitubercular activities .
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Cat. No.: HY-176246
Target:  

Bacterial

Research Areas:  

Infection

Antitubercular agent-52 (Compound 7k) is an antitubercular agent targeting Mycobacterium tuberculosis (Mtb). Antitubercular agent-52 selectively inhibits the cytochrome bcc (cyt-bcc) electron transport chain of Mtb and also acts on cytochrome bd (cyt-bd). Antitubercular agent-52 blocks electron transfer and ATP production by interfering with the key energy metabolism pathway of Mtb. Antitubercular agent-52 is promising for research of tuberculosis .
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Cat. No.: HY-176762
CAS No.: 67047-17-0
Target:  

Topoisomerase

Research Areas:  

Infection Cancer

TOP3B-IN-1 (NSC-260610) is a Topoisomerase IIIβ (TOP3B) inhibitor. TOP3B-IN-1 fails to induce the formation of TOP3B cleavage complexes (TOP3Bccs) with both DNA and RNA, and destabilizes TOP3Bccs. TOP3B-IN-1 can be used as a control compound for the development of inhibitors targeting TOP3B .
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Cat. No.: HY-N15678
CAS No.: 52940-12-2
Synonyms: 1,3,6,8-THAQ
Rheoemodin is an anthraquinone and antibacterial agent. Rheoemodin can be isolated from Cordyceps morakotii BCC 56811. Rheoemodin exhibits antibacterial activity against Acinetobacter baumannii (MIC: 12.5 μg/mL). Rheoemodin also exhibits weak to moderate antimycobacterial and antifungal activity. Rheoemodin also exhibits anticancer activity against breast cancer and small cell lung cancer .
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Cat. No.: HY-N15652
CAS No.: 30270-17-8
Versimide (Compound 15) can be isolated from the insect pathogenic fungus Gibellula sp. BCC36964. Versimide exhibits cytotoxicity in cell lines including MCF-7, KB, NCI-H187, and Vero with IC50s of 3.59, 4.83, 1.89, and 3.49 μg/mL, respectively, demonstrating its anticancer activity .
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Cat. No.: HY-N19150
CAS No.: 2227456-72-4
Cordybislactone hydrolyzed derivative-1 (Compound 4) is a C-7 ester hydrolyzed derivative of Cordybislactone that can be found in the hopper pathogenic fungus Cordyceps sp. BCC 49294 .
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Cat. No.: HY-182711
CAS No.: 1379615-30-1
Target:  

Bacterial Parasite

Research Areas:  

Infection

SCR0911 is an inhibitor of mycobacterial cytochrome bcc oxidase and Plasmodium falciparum cytochrome bc1. SCR0911 disrupts oxidative phosphorylation by binding to mycobacterial cytochrome bcc, binds to the Qi site of Plasmodium falciparum cytochrome bc1, inhibits mycobacterial cell growth and ATP synthesis, and exhibits broad-spectrum anti-mycobacterial and anti-malarial activities. SCR0911 can be used in research related to tuberculosis, malaria, and isolated persistent hypermethioninemia (iph) .
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Cat. No.: HY-183075
CAS No.: 1648720-01-7
Target:  

Bacterial ATP Synthase

Research Areas:  

Infection

ND-011458 is an Antibacterial agent, a QcrB inhibitor, and also an inhibitor of cytochrome bcc:aa3 oxidase function. ND-011458 binds to the QcrB subunit of cytochrome bcc:aa3 oxidase. ND-011458 inhibits ATP formation. When used in combination with Clofazimine (HY-B1046), ND-011458 exhibits bactericidal activity against Mycobacterium abscessus. ND-011458 can be used in studies related to Mycobacterium abscessus pulmonary infections .
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Cat. No.: HY-165368
CAS No.: 519-67-5
Target:  

Bacterial

Atromentin, a phthalide derivative that can be isolated from the wood fungus Hypoxylon fendleri BCC32408, is a selective enoyl-ACP reductase FabK inhibitor with an IC50 of 0.24 μM. Atromentin exhibits selectivity over FabI. Atromentin can be used for antimicrobial research .
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Cat. No.: HY-P706187
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: BCC7; p53; p53 tumor suppressor; Phosphoprotein p5
Species:  
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Cat. No.: HY-P706188
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: BCC7; p53; p53 tumor suppressor; Phosphoprotein p5
Species:  
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Cat. No.: HY-P77778
Purity:  ≥ 95%, as determined by Bis-Tris PAGE.
Synonyms: MHC; HLA-A; P53; TP53; Antigen NY-CO-13; BCC7; FLJ92943; LFS1; TRP53
Species:  
Source:  
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Cat. No.: HY-P77780
Purity:  ≥ 95%, as determined by Bis-Tris PAGE.
Synonyms: MHC; HLA-A; P53; TP53; Antigen NY-CO-13; BCC7; FLJ92943; LFS1; TRP53
Species:  
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Cat. No.: HY-P77779
Purity:  ≥ 95%, as determined by Bis-Tris PAGE.
Synonyms: MHC; HLA-A; P53; TP53; Antigen NY-CO-13; BCC7; FLJ92943; LFS1; TRP53
Species:  
Source:  
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Cat. No.: HY-P77775
Purity:  ≥ 95%, as determined by Bis-Tris PAGE.
Synonyms: MHC; HLA-A; P53; TP53; Antigen NY-CO-13; BCC7; FLJ92943; LFS1; TRP53
Species:  
Source:  
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Cat. No.: HY-P77777
Purity:  ≥ 95%, as determined by Bis-Tris PAGE.
Synonyms: MHC; HLA-A; P53; TP53; Antigen NY-CO-13; BCC7; FLJ92943; LFS1; TRP53
Species:  
Source:  
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