1371 Results for "

2A

" in MedChemExpress (MCE) Product Catalog:
Products (1371)

1371 Results for "2A" in MCE Product Catalog:

21
21 Publications Verification
Cat. No.: HY-P7006
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuBMP-2; BMP2A; BMP-2A; BMP2
Species:  
Source:  
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20
20 Cited Publications
Cat. No.: HY-18983
CAS No.: 101932-71-2
Synonyms: (-)-Calyculin A
Target:  

Phosphatase

Research Areas:  

Cancer

Calyculin A ((-)-Calyculin A) is a potent and cell-permeable protein phosphatase 1 (PP1) and protein phosphatase 2A (PP2A) inhibitor with IC50s of 2 nM and 0.5-1 nM, respectively .
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19
19 Cited Publications
Cat. No.: HY-112929
CAS No.: 1809427-19-7
Purity:  99.83%
Target:  

Phosphatase

Research Areas:  

Cancer

DT-061 is an orally bioavailable activator of protein phosphatase 2A (PP2A) and could be applied in the therapy of KRAS-mutant and MYC-driven tumorigenesis .
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18
18 Cited Publications
Cat. No.: HY-107778
CAS No.: 72882-78-1
Purity:  99.94%
Research Areas:  

Cancer

PF-9366 is a human methionine adenosyltransferase 2A (Mat2A) inhibitor, with an IC50 of 420 nM and a Kd of 170 nM.
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15
15 Cited Publications
Cat. No.: HY-18597
CAS No.: 1632032-53-1
Target:  

Phosphatase

Research Areas:  

Cancer

LB-100 is a protein phosphatase 2A (PP2A) inhibitor, with IC50 of 0.85 μM and 3.87 μM in BxPc-3 and Panc-1 cells [2] .
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12
12 Cited Publications
Cat. No.: HY-14557A
CAS No.: 706782-28-7
Purity:  99.91%
Synonyms: ACP-103 hemitartrate
Target:  

5-HT Receptor

Research Areas:  

Neurological Disease

Pimavanserin (ACP-103) hemitartrate is a potent and brain-penetrant5-HT 2A receptor inverse agonist with pIC50 and pKi of 8.73 and 9.3, respectively.
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12
12 Cited Publications
Cat. No.: HY-N6798
CAS No.: 35891-70-4
Synonyms: Thermozymocidin; ISP-I
Myriocin (Thermozymocidin), a fungal metabolite could be isolated from Myriococcum albomyces, Isaria sinclairi and Mycelia sterilia, is a potent inhibitor of serine-palmitoyl-transferase (SPT) and a key enzyme in de novo synthesis of sphingolipids. Myriocin suppresses replication of both the subgenomic HCV-1b replicon and the JFH-1 strain of genotype 2a infectious HCV, with an IC50 of 3.5 μg/mL for inhibiting HCV infection [2] .
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11
11 Cited Publications
Cat. No.: HY-15789
CAS No.: 1370468-36-2
Purity:  99.97%
Synonyms: MK-8742
Target:  

HCV

Research Areas:  

Infection

Elbasvir (MK-8742) is a hepatitis C virus nonstructural protein 5A (HCV NS5A) inhibitor with EC50s of 4, 3 and 3 nM against genotype 1a, 1b, and 2a, respectively.
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10
10 Cited Publications
Cat. No.: HY-P7022
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuIFN-α2A; IFNA; IFNA2; IFN-a 2A
Species:  
Source:  
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10
10 Cited Publications
Cat. No.: HY-131614
CAS No.: 136186-07-7
Purity:  99.86%
Target:  

Calcium Channel

Research Areas:  

Others

TPC2-A1-N is a powerful and Ca 2+-permeable agonist of two pore channel 2 (TPC2), which plays its role by mimicking the physiological actions of NAADP. TPC2-A1-P reproducibly evokes significant Ca 2+ responses from TPC2 (EC50=7.8 μM), and the effect can be blocked by several TPC blockers. TPC2-A1-N can be used to probe different functions of TPC2 channels in intact cells [2].
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9
9 Cited Publications
Cat. No.: HY-136144
CAS No.: 1391934-98-7
Purity:  98.46%
Research Areas:  

Cancer

FIDAS-5 is a potent and orally active methionine S-adenosyltransferase 2A (MAT2A) inhibitor with an IC50 of 2.1 μM. FIDAS-5 effectively competes against S-adenosylmethionine (SAM) for MAT2A binding. FIDAS-5 has anticancer activities .
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8
8 Cited Publications
Cat. No.: HY-12294A
Purity:  ≥98.0%
Synonyms: NVP-AAM077 tetrasodium hydrate
Target:  

Apoptosis Caspase iGluR

Research Areas:  

Neurological Disease

PEAQX tetrasodium hydrate (NVP-AAM077 tetrasodium hydrate) is a tetrasodium hydrate of PEAQX (HY-12294). PEAQX tetrasodium hydrate is an orally active and selective NMDA antagonist, with IC50 values of 270 nM and 29.6 μM for hNMDAR 1A/2A and hNMDAR 1A/2B, respectively. PEAQX tetrasodium hydrate can promote the activation of caspase-3 and induce cell apoptosis in cortical striatal slice cultures [2].
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8
8 Cited Publications
Cat. No.: HY-15745A
CAS No.: 1621884-22-7
Purity:  99.31%
Target:  

HCV

Research Areas:  

Infection

PSI-7409 tetrasodium is an active 5'-triphosphate metabolite of sofosbuvir (PSI-7977), inhibiting HCV NS5B polymerases, with IC50s of 1.6, 2.8, 0.7 and 2.6 μM for GT 1b_Con1, GT 2a_JFH1, GT 3a, and GT 4a NS5B polymerases, respectively.
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7
7 Cited Publications
Cat. No.: HY-128946
CAS No.: 1279680-68-0
Purity:  99.07%
CL2A-SN-38 is a agent-linker conjugate composed of a potent a DNA Topoisomerase I inhibitor SN-38 and a linker CL2A to make antibody agent conjugate (ADC). CL2A-SN-38 provides significant and specific antitumor effects against a range of human solid tumor types. CL2A-SN-38 uses hydrolyzable linker to deliver active agents within tumor cells and in the tumor microenvironment, resulting in bystander effects .
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6
6 Cited Publications
Cat. No.: HY-131615
CAS No.: 2804595-86-4
Purity:  99.79%
Target:  

Sodium Channel

Research Areas:  

Others

TPC2-A1-P is a powerful and membrane permeable agonist of two pore channel 2 (TPC2) with an EC50 of 10.5 μM. TPC2-A1-P plays its role by mimicking the physiological actions of PI(3,5)P2. TPC2-A1-P also shows higher potency to induce Na 2+ mobilisation from TPC2 than TPC-A1-N (HY-131614). TPC2-A1-P can be used to probe different functions of TPC2 channels in intact cells [2] .
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6
6 Cited Publications
Cat. No.: HY-P80316
Synonyms: AML3, CBFA1, OSF2, PEBP2A, RUNX2, Runt-related transcription factor 2, Acute myeloid leukemia 3 protein, Core-binding factor subunit alpha-1, Oncogene AML-3, Osteoblast-specific transcription factor 2, Polyomavirus enhancer-binding protein 2 alpha A subunit, SL3-3 enhancer factor 1 alpha A subunit, SL3/AKV core-binding factor alpha A subunit, CBF-alpha-1, OSF-2, PEA2-alpha A, PEBP2-alpha A

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP, FC, IF-Tissue, mIHC

Reactivity:  

Human, Mouse, Rat

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5
5 Cited Publications
Cat. No.: HY-124306
CAS No.: 496775-95-2
Purity:  99.75%
Synonyms: CID-888706
Target:  

Ras

Research Areas:  

Cancer

ML-099 (CID-888706) is a pan Ras-related GTPases activator that can activate Rac1, cell division cycle 42, Ras, Rab7, and Rab-2A .
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5
5 Cited Publications
Cat. No.: HY-P99032
CAS No.: 1228763-95-8
Synonyms: IPH2201
Monalizumab (IPH2201) is an immune checkpoint inhibitor targeting Natural Killer Group 2A (NKG2A). Monalizumab, a humanized anti-NKG2A blocking mAb, increases IFN-γ production, thereby promoting NK cell effector functions. Monalizumab can be used for the research of head and neck squamous cell carcinoma (HNSCC) [2].
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5
5 Cited Publications
Cat. No.: HY-P990679

Target:  

Inhibitory Antibodies

Research Areas:  

Inflammation/Immunology Cancer

Rat IgG2a kappa, Isotype Control is a monoclonal antibody derived from rats, representing the immunoglobulin G2a (IgG2a) subclass with a kappa light chain. Rat IgG2a kappa, Isotype Control exhibits high efficiency in inducing K cell mediated cytotoxicity. Rat IgG2a kappa, Isotype Control is utilized in research investigating the roles of different immunoglobulin subclasses in tumor immunology. Rat IgG2a kappa, an isotype control, can be used as an isotype control for Anti-Mouse PD-1 Antibody (RMP1-14) (HY-P99144), Anti-Mouse CD11a/LFA-1α Antibody (M17/4) (HY-P990801), and Anti-Mouse IL-2 Antibody (S4B6-1) (HY-P990796) [2].
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5
5 Cited Publications
Cat. No.: HY-P80920
Synonyms: TREM2; TREM-2; Trem2A; Trem2b; Trem2c; triggering receptor expressed on myeloid cells 2

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF

Reactivity:  

Human, Mouse, Rat

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