47 Results for "

CS1

" in MedChemExpress (MCE) Product Catalog:
Products (47)

47 Results for "CS1" in MCE Product Catalog:

34
34 Publications Verification
製品番号: HY-141511
CAS 番号: 874748-20-6
純度:  97.74%
Coppersensor-1 (CS1) is a membrane-permeable fluorescent dye. Coppersensor-1 has a picomolar affinity for Cu + with high selectivity over competing cellular metalions. Coppersensor-1 as a probe, can selective and sensitive detection of copper(I) ions (Cu +) in biological samples, including live cells. Coppersensor-1 can be used for the research of imaging of severe diseases such as cancer, cardiovascular disorders and neurogenerative diseases [1].
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6
6 Cited Publications
製品番号: HY-B1692
CAS 番号: 15985-39-4
別名: MSX; MSO
Target:  

Glutaminase

研究分野:  

Neurological Disease

L-Methionine-DL-sulfoximine (MSX; MSO), a highly specific and irreversible inhibitor of Glutamine synthetase (GS), is also a potent convulsant which metabolically and morphologically primarily affects astroglia. L-Methionine-DL-sulfoximine has been employed to inhibit the Gln-dependent ammonia-stimulated neuronal toxicity in vitro, potentiating Gln deficit-dependent depression. L-Methionine-DL-sulfoximine tremendously increases the rate of release of fixed nitrogen in cyanobacteria. L-Methionine-DL-sulfoximine is a promising candidate for research in biofertilizers and convulsive seizures (CS) .
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4
4 Cited Publications
製品番号: HY-16276
CAS 番号: 928134-65-0
別名: LCI699
Osilodrostat (LCI699) is a potent, orally active11β-hydroxylase (CYP11B1) inhibitor with an IC50 value of 35 nM. Osilodrostat is a potent, orally aldosterone synthase (CYP11B2) inhibitor with IC50 values of 0.7 nM and 160 nM for human aldosterone synthase and rat aldosterone synthase, respectively. Osilodrostat inhibits aldosterone and corticosterone synthesis. Osilodrostat has blood pressure lowering ability. Osilodrostat can be used for research of Cushing syndrome (CS) .
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4
4 Cited Publications
製品番号: HY-16276A
CAS 番号: 1315449-72-9
別名: LCI699 phosphate
Osilodrostat (LCI699) phosphate is a potent, orally active11β-hydroxylase (CYP11B1) inhibitor with an IC50 value of 35 nM. Osilodrostat phosphate is a potent, orally aldosterone synthase (CYP11B2) inhibitor with IC50 values of 0.7 nM and 160 nM for human aldosterone synthase and rat aldosterone synthase, respectively. Osilodrostat phosphate inhibits aldosterone and corticosterone synthesis. Osilodrostat phosphate has blood pressure lowering ability. Osilodrostat phosphate can be used for research of Cushing syndrome (CS) .
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製品番号: HY-12515CS1
純度:  ≥99.0%
別名: (R)-YC-93-d3 free base
(R)-Nicardipine-d3 is the deuterium labeled R-Nicardipine (HY-12515C) [1].
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製品番号: HY-106950CS1
別名: Diphosphofructose-2-13C sodium; Esafosfan-2-13C sodium; FDP-2-13C sodium
Fosfructose-2- 13C (sodium) is the 13C labeled Fosfructose [1].
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製品番号: HY-B0311CS1
CAS 番号: 1185134-76-2
(Rac)-Carbidopa-d5 is a deuterium labeled compound.
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製品番号: HY-43962
CAS 番号: 693227-00-8
別名: Androgen receptor ligand 3
CS-1-65 is an androgen receptor (AR) ligand. CS-1-65 is linked to an IAP ligand via a linker to form an ERα PROTAC degrader.
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製品番号: HY-137005
CAS 番号: 1448009-94-6
Target:  

Topoisomerase Apoptosis

研究分野:  

Cancer

CS1 is a potent DNA Topo II α inhibitor. CS1 displays broad-spectrum in vitro antitumor effects, low toxicity in vivo and potential anti-multidrug resistance capabilities. CS1 leads to DNA damage, cell cycle arrest at G2/M phase and apoptosis [1].
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製品番号: HY-P99454
CAS 番号: 1826819-58-2
別名: ABBV-838
研究分野:  

Cancer

Azintuxizumab vedotin (ABBV-838) is an antibody–drug conjugate (ADC) targeting a unique epitope of CD2 subset 1, a cell-surface glycoprotein expressed on multiple myeloma cells [1].
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製品番号: HY-P1816
CAS 番号: 136466-51-8
Target:  

Integrin

研究分野:  

Cancer

The connecting segment 1 (CS-1) is a cell attachment domain located in the type III homology connecting segment (IIICS) of fibronectin. Fibronectin CS1 Peptide lacks the Arg-Gly-Asp-containing domain, actively inhibits tumor metastases in spontaneous and experimental metastasis models [1].
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製品番号: HY-P990644

Target:  

阻害性抗体

研究分野:  

Inflammation/Immunology

PDL-241 is a humanized antibody expressed in CHO that targets SLAMF7/CS1. PDL-241 has a huIgG1 heavy chain and a huκ light chain, with a predicted molecular weight (MW) of 146.38 kDa. The isotype control for PDL-241 can refer to Human IgG1 kappa, Isotype Control (HY-P99001).
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製品番号: HY-179238
Target:  

Estrogen Receptor/ERR

研究分野:  

Cancer

CS-1-103 is a potent estrogen receptor (ER) TRACER (transcriptional regulation via active control of epigenetic reprogramming). CS-1-103 inhibits ER transcriptional activity with an EC50 of 0.36 μM by recruiting methyl-CpG binding domain protein 2 (MBD2), HDACs and the nucleosome remodeling and deacetylase (NuRD) complex. CS-1-103 can be used for breast and prostate cancer research [1].
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製品番号: HY-P84817
別名: 19A; CS1; SLAMF7; CRACC

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human, Mouse, Rat, Monkey, Rabbit

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製品番号: HY-P84817A
別名: 19A; CS1; SLAMF7; CRACC

Host:  

Mouse

Application:  

WB, IHC-P, FC, ELISA

Reactivity:  

Human, Mouse, Rat, Monkey, Rabbit

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製品番号: HY-P81747
別名: SLAM7 (19A; CD319; CRACC; CS1)

Host:  

Rabbit

Application:  

FC, ELISA

Reactivity:  

Human

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製品番号: HY-P78642
純度:  ≥ 90%, as determined by reducing SDS-PAGE.
別名: SLAMF7; CD319; CS1; CRACC; 19A; FOAP-12
Species:  
Source:  
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製品番号: HY-P88880
別名: 19A; CD319; CRACC; CS1

Host:  

Mouse

Application:  

IHC-P, FC

Reactivity:  

Human

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製品番号: HY-P81432
別名: 19A; CS1; SLAMF7; SLAM family member 7

Host:  

Rabbit

Application:  

IHC-P

Reactivity:  

Human

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製品番号: HY-P88880A
別名: 19A; CD319; CRACC; CS1

Host:  

Mouse

Application:  

IHC-P, FC

Reactivity:  

Human

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