1388 Results for "

Allosteric

" in MedChemExpress (MCE) Product Catalog:
Products (1388)

1388 Results for "Allosteric" in MCE Product Catalog:

11
11 Cited Publications
Cat. No.: HY-116009
CAS No.: 2172651-73-7
Purity:  99.56%
Target:  

SHP2 Phosphatase

Research Areas:  

Cancer

RMC-4550 is a potent, selective and allosteric inhibitor of SHP2, with an IC50 of 0.583 nM.
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11
11 Cited Publications
Cat. No.: HY-17537
CAS No.: 1216665-49-4
Target:  

IRE1

Research Areas:  

Cancer

APY29, an ATP-competitive inhibitor, is an allosteric modulator of IRE1α which inhibits IRE1α autophosphorylation by binding to the ATP-binding pocket with IC50 of 280 nM. APY29 acts as a ligand that allosterically activates IRE1α adjacent RNase domain .
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11
11 Cited Publications
Cat. No.: HY-101068
CAS No.: 54857-86-2
Purity:  99.59%
Synonyms: RMI14514; MDL14514
Research Areas:  

Cancer

TOFA (RMI14514;MDL14514) is an allosteric inhibitor of acetyl-CoA carboxylase-α (ACCA ).
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11
11 Cited Publications
Cat. No.: HY-12682
CAS No.: 311795-38-7
Purity:  99.88%
Synonyms: Compound 968
Target:  

Glutaminase

Research Areas:  

Cancer

Glutaminase C-IN-1 (Compound 968) is an allosteric inhibitor of Glutaminase C that inhibits cancer cell growth without affecting their normal cellular counterparts .
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11
11 Cited Publications
Cat. No.: HY-137067
CAS No.: 2304621-06-3
Purity:  99.45%
Synonyms: LDC203974
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

IMT1B (LDC203974) is an orally active, noncompetitive and specific allosteric inhibitor of mitochondrial RNA polymerase (POLRMT) and inhibits mitochondrial DNA (mtDNA) expression. IMT1B has anti-tumour effects .
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10
10 Cited Publications
Cat. No.: HY-12042
CAS No.: 1236699-92-5
Purity:  99.88%
Synonyms: AS703026; MSC1936369B
Target:  

MEK

Research Areas:  

Cancer

Pimasertib (AS703026) is a highly selective, ATP non-competitive allosteric orally available MEK1/2 inhibitor .
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10
10 Cited Publications
Cat. No.: HY-119339
CAS No.: 1648843-04-2
Purity:  99.67%
Target:  

CXCR

SX-682 is an orally bioavailable, potent allosteric inhibitor of CXCR1 and CXCR2. SX-682 can block tumor myeloid-derived suppressor cells (MDSCs) recruitment and enhance T cell activation and antitumor immunity .
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9
9 Cited Publications
Cat. No.: HY-114164C
CAS No.: 9002-04-4
Purity:  88.00%
Rabbit Thrombin is a Na +-activated, allosteric serine protease that plays opposing functional roles in blood coagulation. Thrombin recognition sequence and can be used to digest GST-tagged proteins .
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9
9 Cited Publications
Cat. No.: HY-114164D
CAS No.: 9002-04-4
Target:  

Thrombin

Research Areas:  

Cardiovascular Disease

Rat Thrombin is a Na +-activated, allosteric serine protease that plays opposing functional roles in blood coagulation. Thrombin recognition sequence and can be used to digest GST-tagged proteins .
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9
9 Cited Publications
Cat. No.: HY-114164
CAS No.: 9002-04-4
Target:  

Thrombin

Research Areas:  

Neurological Disease

Thrombin (MW 37kDa) is a Na +-activated, allosteric serine protease that plays opposing functional roles in blood coagulation. Thrombin recognition sequence and can be used to digest GST-tagged proteins.
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8
8 Cited Publications
Cat. No.: HY-136173
CAS No.: 1801765-04-7
Purity:  99.41%
Synonyms: TNO155
Target:  

SHP2 Phosphatase

Research Areas:  

Cancer

Batoprotafib (TNO155) is a potent selective and orally active allosteric inhibitor of wild-type SHP2 (IC50=0.011 µM). Batoprotafib has the potential for the study of RTK-dependent malignancies, especially advanced solid tumors .
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8
8 Cited Publications
Cat. No.: HY-115627
CAS No.: 2143896-83-5
Purity:  99.94%
Synonyms: GPX4-Activator-1d4
Research Areas:  

Inflammation/Immunology

PKUMDL-LC-101-D04 (GPX4-Activator-1d4) is a glutathione peroxidase 4 (GPX4) allosteric activator (pEC50=4.7). PKUMDL-LC-101-D04 can inhibit ferroptosis and inflammation .
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8
8 Cited Publications
Cat. No.: HY-112769
CAS No.: 1219739-36-2
Purity:  98.92%
Target:  

AMPK

Research Areas:  

Metabolic Disease

EX229, a Benzimidazole derivative, is a potent and allosteric activator of AMP-activated protein kinase (AMPK), with Kds of 0.06 μM, 0.06 μM and 0.51 μM for α1β1γ1, α2β1γ1 and α1β2γ1 in biolayer interferometry, respectively.
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7
7 Cited Publications
Cat. No.: HY-10167A
CAS No.: 177172-49-5
Purity:  99.66%
Synonyms: R-568 hydrochloride; NPS R-568
Target:  

CaSR

Research Areas:  

Others

Tecalcet Hydrochloride (R 568 Hydrochloride), an orally active calcimimetic compound, allosterically and positively modulates the calcium-sensing receptor (CaSR). Tecalcet Hydrochloride (R 568 Hydrochloride) increases the sensitivity to activation by extracellular Ca 2+ .
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6
6 Cited Publications
Cat. No.: HY-13449
CAS No.: 1035555-63-5
Purity:  99.79%
Target:  

MEK

Research Areas:  

Cancer

TAK-733 is a potent and selective MEK allosteric site inhibitor with an IC50 of 3.2 nM.
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6
6 Cited Publications
Cat. No.: HY-59047
CAS No.: 41964-07-2
Synonyms: MLR-1023
Target:  

Src

Research Areas:  

Metabolic Disease

Tolimidone is a potent and selective allosteric activator of Lyn kinase with an EC50 of 63 nM.
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6
6 Cited Publications
Cat. No.: HY-18652
CAS No.: 946128-88-7
Synonyms: Ro 5126766; CH5126766
Target:  

MEK Raf

Research Areas:  

Cancer

Avutometinib (Ro 5126766) is a first-in-class dual MEK/RAF inhibitor that allosterically inhibits BRAF V600E, CRAF, MEK, and BRAF (IC50: 8.2, 56, 160 nM, and 190 nM, respectively).
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6
6 Cited Publications
Cat. No.: HY-P1125
CAS No.: 300851-67-6
Research Areas:  

Others

4-CMTB is a selective free fatty acid receptor 2 (FFA2/GPR43) agonist and a positive allosteric modulator (pEC50=6.38) .
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6
6 Cited Publications
Cat. No.: HY-12429
CAS No.: 958002-33-0
Purity:  99.94%
Synonyms: BMS-791325
Target:  

DNA/RNA Synthesis HCV

Research Areas:  

Infection

Beclabuvir is an allosteric inhibitor that binds to thumb site 1 of the hepatitis C virus (HCV) NS5B RNA-dependent RNA polymerase, and inhibits recombinant NS5B proteins from HCV genotypes 1, 3, 4, and 5 with IC50 of < 28 nM .
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6
6 Cited Publications
Cat. No.: HY-50688
CAS No.: 211096-49-0
Target:  

CXCR

Research Areas:  

Inflammation/Immunology

SB-265610 is a selective, competitive, nonpeptide and allosteric CXCR2 antagonist. SB-265610 blocks rat cytokine-induced neutrophil chemoattractant-1 (CINC-1)-induced calcium mobilization and neutrophil chemotaxis with IC50s of 3.7 nM and 70 nM, respectively .
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