12 Results for "

NSD1

" in MedChemExpress (MCE) Product Catalog:
Products (12)

12 Results for "NSD1" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-134086
CAS No.: 2351225-46-0
Purity:  97.76%
Research Areas:  

Cancer

NSD-IN-2 is a potent and irreversible NSD inhibitor with inhibitory activity towards members of the NSD family (NSD1/2/3). NSD-IN-2 can be used in research of acute myeloid leukemia [1].
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Cat. No.: HY-121093
CAS No.: 303141-21-1
Purity:  99.73%
Research Areas:  

Cancer

DC-S239 is a selective histone methyltransferase SET7 inhibitor with an IC50 value of 4.59 μM. DC-S239 also displays selectivity for DNMT1, DOT1L, EZH2, NSD1, SETD8 and G9a. DC-S239 has anticancer activity [1].
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Cat. No.: HY-114340
CAS No.: 1814881-70-3
Purity:  98.06%
Research Areas:  

Cancer

LEM-14 is a potent and selective NSD2 inhibitor with an IC50 of 132 µM. LEM-14 has very weak activitv against NSD1 and has no activity against NSD3. LEM-14 inhibits fibrotic gene expression in ND but not DIO BMDMs. LEM-14 combined with ionizing radiation (IR) enhances the apoptosis rate and reduces the colony-formation ability of CRC cells. LEM-14 exhibits enhanced anti-tumor efficacy in Balb/c nude mice bearing LoVo cell xenografts when combined with ionizing radiation. LEM-14 has the potential for the research of multiple myeloma and colorectal cancer [1] .
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Cat. No.: HY-125244
CAS No.: 2987501-17-5
Purity:  99.57%
Research Areas:  

Cancer

LEM-14-1189, a LEM-14 (HY-114340) derivative, is a NSDs inhibitor with IC50s of 418 μM (NSD1), 111 μM (NSD2), and 60 μM (NSD3), respectively. The NSDs, histone lysine methyltransferases (HMTases), are oncoproteins, drivers of a number of tumors. LEM-14-1189 can be used for multiple myeloma (MM) research [1].
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Cat. No.: HY-RS09587
Research Areas:  

Others

NSD1 Human Pre-designed siRNA Set A contains three designed siRNAs for NSD1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS18628
Research Areas:  

Others

Nsd1 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Nsd1 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS25114
Research Areas:  

Others

Nsd1 Rat Pre-designed siRNA Set A contains three designed siRNAs for Nsd1 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-W649594
CAS No.: 22978-55-8
Research Areas:  

Inflammation/Immunology Cancer

NR2F6 modulator-2 (Compound I) is an autorepressed orphan nuclear receptor NR2F6 (Nuclear Receptor subfamily 2 group F member 6) modulator. NR2F6 modulator-2 can inhibits the recruitment of the bio-NSD1 peptide with an IC50 of 2.0 equivalents of NR2F6. NR2F6 modulator-2 can be used for the researches of cancer and immunology [1].
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Cat. No.: HY-177400
CAS No.: 3034213-62-9
Research Areas:  

Cancer

NSD-IN-5 is a nuclear receptor-binding SET domain (NSD) inhibitor with IC50 values of 6 nM and < 1 nM against NSD1 and NSD2, respectively. NSD-IN-5 can be used in research related to multiple myeloma [1].
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Cat. No.: HY-P85445
Synonyms: NSD1; ARA267; KMT3B; Histone-lysine N-methyltransferase; H3 lysine-36 and H4 lysine-20 specific; Androgen receptor coactivator 267 kDa protein; Androgen receptor-associated protein of 267 kDa; H3-K36-HMTase; H4-K20-HMTase; Lysine N-methyltr

Host:  

Mouse

Application:  

WB

Reactivity:  

Human

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Cat. No.: HY-180553
Research Areas:  

Cancer

NSD2-IN-6 is a selective and orally active NSD2 inhibitor with IC50s of 3.8  and 274 nM for NSD2 and NSD1 respectively. NSD2-IN-6 reduces H3K36me2 levels, reverses cell plasticity by restoring the androgen receptor ( AR) signaling pathway. NSD2-IN-6 reduces a shift from cluster 2 and 3 states towards the cluster 1 state in organoids. NSD2-IN-6 exerts antitumor activity by reversing tumor cell plasticity, suppressing growth, and promoting apoptosis in vivo. NSD2-IN-6 can be used for prostate cancer research [1].
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Cat. No.: HY-133567
CAS No.: 2567886-53-5
SET7-IN-DC21 is a selective, potent SET7 inhibitor (IC50 = 15.93 μM; KD = 18.00 μM). SET7-IN-DC21 has good selectivity for several other epigenetic targets, such as SUV39H1, G9a, NSD1, DOT1L and MOF. SET7-IN-DC21 can be used for the researches of cancer, infection, inflammation, metabolic and cardiovascular disease, such as breast cancer [1].
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