1101 Results for "

Small molecule

" in MedChemExpress (MCE) Product Catalog:
Products (1101)

1101 Results for "Small molecule" in MCE Product Catalog:

126
126 Publications Verification
Cat. No.: HY-W090090
CAS No.: 121207-31-6
Synonyms: Pyrromethene 546
BODIPY493/503 is a BODIPY dye. BODIPY dye is a small molecule dye with strong ultraviolet absorption ability, its fluorescence peak is relatively sharp, and the quantum yield is high. They are relatively insensitive to the polarity and pH of the environment and are relatively stable under different physiological conditions. Due to its structural asymmetry, BODIPY derives a variety of structural products. BODIPY lipid droplet dyes can well pass through the cell membrane into the cell, and localize the neutral lipids in the cell to specifically stain the lipid droplets, which can be used for labeling of live cells and fixed cells . Maximum excitation/emission wavelength: 493/503 nm .
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74
74 Cited Publications
Cat. No.: HY-19707
CAS No.: 14003-96-4
Synonyms: IRE1 Inhibitor III
Target:  

IRE1

Research Areas:  

Metabolic Disease

4μ8C (IRE1 Inhibitor III) is a small-molecule inhibitor of IRE1α.
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45
45 Cited Publications
Cat. No.: HY-D0819
CAS No.: 146368-14-1
Synonyms: Cy5 NHS Ester; Sulfo-Cyanine5 Succinimidyl Ester
Cy5-SE (Cy5 NHS Ester) is a reactive dye for the labeling of amino-groups in peptides, proteins, and oligonucleotides. This dye requires small amount of organic co-solvent (such as DMF or DMSO) to be used in labeling reaction. This reagent is ideal for very cost-efficient labeling of soluble proteins, as well as all kinds of peptides and oligonucleotides. This reagent also works well in organic solvents for small molecule labeling. Excitation (nm):649, Emission (nm): 670.
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31
31 Cited Publications
Cat. No.: HY-19708
CAS No.: 1589527-65-0
Target:  

IRE1

KIRA6 is an advanced small-molecule IRE1α RNase kinase inhibitor with an IC50 of 0.6 µM . KIRA6 can trigger an apoptotic response .
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23
23 Cited Publications
Cat. No.: HY-50295
CAS No.: 212631-79-3
Synonyms: PD 184352
Target:  

MEK Apoptosis

Research Areas:  

Cancer

CI-1040 (PD 184352) is an orally active, highly specific, small-molecule inhibitor of MEK with an IC50 of 17 nM for MEK1.
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23
23 Cited Publications
Cat. No.: HY-D1614
CAS No.: 216434-81-0
Target:  

Fluorescent Dye

Research Areas:  

Others

BODIPY493/503 methyl bromide is a BODIPY dye. BODIPY dye is a small molecule dye with strong ultraviolet absorption ability, its fluorescence peak is relatively sharp, and the quantum yield is high. They are relatively insensitive to the polarity and pH of the environment and are relatively stable under different physiological conditions. Due to its structural asymmetry, BODIPY derives a variety of structural products. BODIPY lipid droplet dyes can well pass through the cell membrane into the cell, and localize the neutral lipids in the cell to specifically stain the lipid droplets, which can be used for labeling of live cells and fixed cells . Maximum excitation/emission wavelength: 493/503 nm .
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21
21 Cited Publications
Cat. No.: HY-16291
CAS No.: 916151-99-0
Synonyms: LOR-253; LT-253
Target:  

c-Myc KLF Apoptosis

Research Areas:  

Inflammation/Immunology Cancer

APTO-253 (LOR-253) is a small molecule that inhibits c-Myc expression, stabilizes G-quadruplex DNA, and induces cell cycle arrest and apoptosis in acute myeloid leukemia cells. APTO-253 mediates anticancer activity through induction of the Krüppel-like factor 4 (KLF4) tumor suppressor . APTO-253 has antiarthritic activity .
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20
20 Cited Publications
Cat. No.: HY-16438
CAS No.: 925206-65-1
Synonyms: Nibrozetone
RRx-001, a hypoxia-selective epigenetic agent and studied as a radio- and chem-sensitizer, triggers apoptosis and overcomes agent resistance in myeloma. RRx-001 exhibits potent anti-tumor activity with minimal toxicity . RRx-001 is a dual small molecule checkpoint inhibitor by downregulating CD47 and SIRP-α . RRx-001 is a potent inhibitor of G6PD and shows potent antimalarial activity .
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16
16 Cited Publications
Cat. No.: HY-101091
CAS No.: 662163-81-7
Purity:  99.71%
Target:  

Apoptosis

Research Areas:  

Cancer

Importazole is a small molecule inhibitor of the nuclear transport receptor importin-β.
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16
16 Cited Publications
Cat. No.: HY-12302
CAS No.: 142273-20-9
Purity:  98.20%
Synonyms: 9-Bromopaullone; NSC-664704
Target:  

CDK GSK-3

Research Areas:  

Cancer

Kenpaullone is a potent inhibitor of CDK1/cyclin B and GSK-3β, with IC50s of 0.4 μM and 23 nM, and also inhibits CDK2/cyclin A, CDK2/cyclin E, and CDK5/p25 with IC50s of 0.68 μM, 7.5 μM, 0.85 μM, respectively. Kenpaullone, a small molecule inhibitor of KLF4, reduces self-renewal of breast cancer stem cells and cell motility in vitro.
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14
14 Cited Publications
Cat. No.: HY-150031
CAS No.: 694488-83-0
Purity:  99.44%
Research Areas:  

Others

MFI8 is a small molecule inhibitor of mitochondrial .
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13
13 Cited Publications
Cat. No.: HY-19980
CAS No.: 5291-32-7
Synonyms: APR-246; PRIMA-1Met
Research Areas:  

Cancer

Eprenetapopt (APR-246) is a first-in-class, small molecule that restores wild-type p53 functions in TP53-mutant cells. Eprenetapopt triggers apoptosis in tumor cells. Eprenetapopt also targets the selenoprotein thioredoxin reductase 1 (TrxR1), a key regulator of cellular redox balance .
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13
13 Cited Publications
Cat. No.: HY-129039
CAS No.: 778649-18-6
Purity:  99.58%
Synonyms: MB-3
Butyrolactone 3 (MB-3) is a specifical small-molecule inhibitor of the histone acetyltransferase Gcn5 (IC50=100 μM), which has a high affinity to the Gcn5 enzyme comparable to that of its natural substrate, histone H3. Butyrolactone 3 shows weak inhibitory on CBP (IC50=0.5 mM). Butyrolactone 3 can be used in studies of cancer, metabolic, autoimmune and neurological diseases .
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12
12 Cited Publications
Cat. No.: HY-100493
CAS No.: 1334493-07-0
Purity:  99.52%
Target:  

STAT

Research Areas:  

Cancer

BP-1-102 is an orally available, small-molecule inhibitor of transcription factor Stat3, with an IC50 of 6.8 μM.
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12
12 Cited Publications
Cat. No.: HY-106101
CAS No.: 512-64-1
Purity:  98.57%
Synonyms: Quinomycin A; NSC-13502
Research Areas:  

Cancer

Echinomycin (Quinomycin A) is potent small-molecule and cell-permeable inhibitor of hypoxia-inducible factor-1 (HIF-1) DNA-binding activity. Echinomycin selectively inhibits the cancer stem cells (CSCs) with an IC50 of 29.4 pM .
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10
10 Cited Publications
Cat. No.: HY-103665
CAS No.: 2138299-29-1
Purity:  99.90%
Target:  

STING

Research Areas:  

Cancer

STING agonist-3, extracted from patent WO2017175147A1 (example 10), is a selective and non-nucleotide small-molecule STING agonist with a pEC50 and pIC50 of 7.5 and 9.5, respectively. STING agonist-3 has durable anti-tumor effect and tremendous potential to improve treatment of cancer .
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10
10 Cited Publications
Cat. No.: HY-103665A
Purity:  98.36%
Target:  

STING

Research Areas:  

Cancer

STING agonist-3 trihydrochloride, extracted from patent WO2017175147A1 (example 10), is a selective and non-nucleotide small-molecule STING agonist with a pEC50 and pEC50 of 7.5 and 9.5, respectively. STING agonist-3 trihydrochloride has durable anti-tumor effect and tremendous potential to improve treatment of cancer .
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9
9 Cited Publications
Cat. No.: HY-K1043

MCE CEPT Cocktail is composed of CET small molecules (Chroman 1, Emricasan and Trans-ISRIB) and Polyamine Solution, and can effectively enhance cell survival and promote clonal growth of genetically stable hPSCs.


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8
8 Cited Publications
Cat. No.: HY-16925
CAS No.: 1857417-13-0
Research Areas:  

Cancer

MI-503 is a highly potent and orally bioavailable small molecule inhibitor of the menin-mLL interaction.
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8
8 Cited Publications
Cat. No.: HY-131296
CAS No.: 2677841-58-4
Purity:  98.98%
Target:  

Drug Derivative

Research Areas:  

Inflammation/Immunology

5-A-RU-PABC-Val-Cit-Fmoc is the proagent of 5-A-RU . 5-A-RU, a precursor of bacterial Riboflavin, is a mucosal-associated invariant T (MAIT) cells activator. 5-A-RU forms potent MAIT-activating antigens via non-enzymatic reactions with small molecules, such as glyoxal and methylglyoxal, which are derived from other metabolic pathways .
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