639 Results for "

SCO2 mutations

" in MedChemExpress (MCE) Product Catalog:
Products (639)

639 Results for "SCO2 mutations" in MCE Product Catalog:

Cat. No.: HY-101243
CAS No.: 1345098-78-3
Purity:  98.20%
Target:  

Tyrosinase

Research Areas:  

Cancer

XMD16-5 is a potent TNK2 inhibitor with IC50 values of 16 and 77 nM for the D163E and R806Q mutations, respectively.
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Cat. No.: HY-15811
CAS No.: 1234480-46-6
Purity:  99.57%
Synonyms: ACK1-B19
Target:  

Tyrosinase

Research Areas:  

Cancer

XMD8-87 is a potent TNK2 inhibitor with IC50 values of 38 and 113 nM for the D163E and R806Q mutations, respectively.
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Cat. No.: HY-176489
CAS No.: 3043908-63-7
Target:  

PROTACs Ras

Research Areas:  

Cancer

PROTAC pan-KRAS degrader-1 is a pan-KRAS-targeting PROTAC degrader for degrading different KRAS mutation types, such as G12D, G12C, G12V, and G13D. PROTAC pan-KRAS degrader-1 potently degrades KRAS mutation (G12D) in AGS cells, with a DC50 of 1.1 nM, Dmax of 95%. PROTAC pan-KRAS degrader-1 can be used to search diseases caused by KRAS mutation or amplification, especially cancers such as breast cancer, bladder cancer, gastric cancer, etc .
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Cat. No.: HY-152852
CAS No.: 1639014-72-4
Purity:  99.40%
Synonyms: Mifanertinib
Target:  

EGFR

Research Areas:  

Cancer

Mefatinib free base (Mifanertinib) is an orally active EGFR and HER2 kinase inhibitor with IC50 values of 0.4 nM and 11.7 nM, respectively. Mefatinib free base inhibits tumor growth in mouse models of lung cancer xenografts that overexpress EGFR/HER2, carry EGFR mutations, or carry Erlotinib (HY-50896)-resistant EGFR double mutations. Mefatinib free base can be used for the research of advanced EGFR-mutant non-small cell lung cancer .
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Cat. No.: HY-RS12557
Research Areas:  

Others

SCO2 Human Pre-designed siRNA Set A contains three designed siRNAs for SCO2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS20816
Research Areas:  

Others

Sco2 Mouse Pre-designed siRNA Set A contains three designed siRNAs for Sco2 gene (Mouse), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-RS27330
Research Areas:  

Others

Sco2 Rat Pre-designed siRNA Set A contains three designed siRNAs for Sco2 gene (Rat), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-N12109
CAS No.: 585-23-9
Albizziin is an amino acid analog with activity as a competitive inhibitor of asparagine synthetase. Albizziin has been used to isolate Chinese hamster ovary cell mutants with altered levels of the target enzyme. Several mutational classes of albizziin can be distinguished based on cross-resistance to β-aspartic hydroxamic acid. Studies on asparagine synthetase have shown that resistance to albizziin may be associated with altered regulation of asparagine synthetase, structural mutations of the enzyme, and gene amplification .
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Cat. No.: HY-128572
CAS No.: 2377141-31-4
Purity:  99.14%
Target:  

FLT3

Research Areas:  

Cancer

FLT3-IN-6 is a potent and selective inhibitor of FLT3-ITD (FLT3 mutation) with an IC50 of 1.336 nM .
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Cat. No.: HY-115741
CAS No.: 956025-99-3
Purity:  ≥99.0%
3BrB-PP1 is an ATP-competitive analog. 3BrB-PP1 can specifically inhibit the activity of protein kinase with mutations in the ATP-binding pocket (mutation of Thr97 within Sty1’s ATP-binding pocket) [2].
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Cat. No.: HY-135887
CAS No.: 2254805-62-2
Purity:  98.59%
ZX-29 is a potent and selective ALK inhibitor with an IC50 of 2.1 nM, 1.3 nM and 3.9 nM for ALK, ALK L1196M and ALK G1202R mutations, respectively. ZX-29 is inactive against EGFR. ZX-29 induces apoptosis by inducing endoplasmic reticulum (ER) stress and overcomes cell resistance caused by an ALK mutation. ZX-29 also induces protective autophagy and has antitumor effect .
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Drisapersen sodium
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RNA, (P-thio)(Um-Cm-Am-Am-Gm-Gm-Am-Am-Gm-Am-Um-Gm-Gm-Cm-Am-Um-Um-Um-Cm-Um), sodium salt
Cat. No.: HY-145724A
CAS No.: 1181666-20-5
Purity:  96.05%
Synonyms: Kyndrisa sodium; GSK2402968A sodium; PRO051 sodium
Drisapersen sodium, a antisense oligonucleotide, induces exon 51 skipping during dystrophin pre-mRNA splicing and allows synthesis of partially functional dystrophin in Duchenne muscular dystrophy (DMD) patients with amenable mutations.
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Sepofarsen
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RNA, (P-thio)(Gm-Gm-Um-Gm-Gm-Am-Um-Cm-Am-Cm-Gm-Am-Gm-Um-Um-Cm-Am)
Cat. No.: HY-153496
CAS No.: 2227173-68-2
Synonyms: QR 110
Sepofarsen (QR-110) is an RNA antisense oligonucleotide targeting to the p.Cys998X mutation (also known as the c.2991+1655A>G mutation) in the CEP290 gene.
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Cat. No.: HY-174387
CAS No.: 2941104-53-4
Target:  

c-Met/HGFR

Research Areas:  

Cancer

KIN-8741 is a highly selective Type IIb c-Met inhibitor. KIN-8741 has broad activity against c-Met kinase mutations. KIN-8741 shows antitumor activity in MET gene amplified and exon 14 deleted non-small cell lung cancer models. KIN-8741 can be used in the research of c-Met driven cancers, especially advanced tumors carrying MET exon 14 jump mutations, acquired drug resistance mutations, etc .
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Cat. No.: HY-145937
CAS No.: 2413987-20-7
Purity:  98.50%
Target:  

MDM-2/p53

Research Areas:  

Cancer

PK9327 is a small-molecule stabilizer targeting cavity-creating p53 cancer mutations.
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Cat. No.: HY-400785
CAS No.: 2452300-94-4
Target:  

Drug Derivative

Research Areas:  

Cancer

Dapagliflozin impurity A (Compound A) is a dapagliflozin peroxide, a genotoxic impurity, can cause damage to human genetic material at very low concentrations, leading to genetic mutations and possibly tumorigenesis .
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Cat. No.: HY-172552
CAS No.: 3038234-95-3
Target:  

DNA/RNA Synthesis

Research Areas:  

Metabolic Disease

RECTAS-2.0 is a small molecule designed to correct RNA mis-splicing caused by the GLA c.639+919G>A mutation, used for the research of Fabry disease .
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Cat. No.: HY-P1828
CAS No.: 129112-17-0
Target:  

EGFR

Research Areas:  

Cancer

EGFRvIII peptide (PEPvIII) is a tumor-specific mutation that is widely expressed in glioblastoma multiforme (GBM) and other neoplasms and its expression enhances tumorigenicity. EGFRvIII peptide represents a truly tumor-specific target for antitumor immunotherapy .
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Cat. No.: HY-P87066
Synonyms: SCO2

Host:  

Rabbit

Application:  

WB, IHC-P, ICC/IF, IP

Reactivity:  

Human, Mouse, Rat

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Cat. No.: HY-123359
CAS No.: 414909-09-4
Research Areas:  

Others

RTC14 is a read-through compound (RTC) that can induce ribosomes to bypass nonsense mutations in mRNA and allow the production of full-length functional proteins. RTC14 has the potential to be used in the research of various genetic disorders, such as nonsense mutations in the ataxia-telangiectasia mutated (ATM) gene and the dystrophin gene .
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