13 Results for "

schwannoma

" in MedChemExpress (MCE) Product Catalog:
Products (13)

13 Results for "schwannoma" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-15827
CAS No.: 7497-07-6
Purity:  99.63%
Target:  

MMP

Research Areas:  

Cardiovascular Disease Cancer

NSC 405020 is a specific MMP14 inhibitor. NSC 405020 can directly interact with the hemopexin domain of MMP14. NSC 405020 reduces the expression of full length and active cleaved Notch3 (NICD3). NSC 405020 can be used to research vestibular schwannoma, hemostasis and thrombosis .
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3
3 Cited Publications
Cat. No.: HY-P7002
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: AREG; AR; Prev. AREGB; schwannoma-Derived Growth Factor; Prev. SDGF; Amphiregulin B; CRDGF; Amphiregulin; Colorectum Cell-Derived Growth Factor
Species:  
Human
Source:  
HEK293
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2
2 Cited Publications
Cat. No.: HY-P77868
Purity:  ≥ 90%, as determined by Bis-Tris PAGE.
Synonyms: AREG; AR; Prev. AREGB; schwannoma-Derived Growth Factor; Prev. SDGF; Amphiregulin B; CRDGF; Amphiregulin; Colorectum Cell-Derived Growth Factor
Species:  
Mouse
Source:  
HEK293
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Cat. No.: HY-400902
CAS No.: 2506273-81-8
Target:  

YAP VEGFR Hippo (MST)

Research Areas:  

Cancer

VT3989 is an orally active pan-TEAD autopalmitoylation inhibitor that modulates the Hippo signaling pathway. VT3989 directly binds to TEAD transcription factors to block their palmitoylation modification, thereby disrupting the formation of YAP/TAZ-TEAD complexes and inhibiting downstream oncogenic transcriptional activity. VT3989 effectively inhibits the growth of NF2-deficient schwannoma and meningioma cells and reverses the Schwann cell phenotype. In addition, VT3989 exerts a synergistic effect when combined with Osimtinib (HY-15772) in EGFR-mutant non-small cell lung cancer models, significantly delaying tumor recurrence and prolonging survival. VT3989 can be used for the research of epithelioid hemangioendothelioma, malignant pleural mesothelioma, type 2 neurofibromatosis and related advanced solid tumors .
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Cat. No.: HY-110085
CAS No.: 6088-51-3
Purity:  98.49%
Synonyms: DDD; Bis(6-hydroxy-2-naphthyl)disulfide; PIR-3.5
Target:  

PAK

Research Areas:  

Cancer

2,2′-Dihydroxy-6,6′-dinaphthyl disulfide (PIR-3.5) is a PAK1 inhibitor .
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Cat. No.: HY-107662
CAS No.: 34320-83-7
Purity:  99.72%
Target:  

Apoptosis

Research Areas:  

Infection Cancer

TCS PrP Inhibitor 13, an antiprion agent, is a cellular prion protein (PrP C) inhibitor. TCS PrP Inhibitor 13, as a protease-resistant form of prion protein (PrP-res) accumulation inhibitor, shows an IC50 value of 3 nM in both ScN2a and F3 cell lines. TCS PrP Inhibitor 13 induces Schwannoma cells apoptosis .
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Cat. No.: HY-120614
CAS No.: 167467-53-0
Target:  

Farnesyl Transferase

Research Areas:  

Cancer

BMS-186511 is a farnesyltransferase (FT) inhibitor and shows anticancer activity .
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Cat. No.: HY-W259575
CAS No.: 70035-83-5
Research Areas:  

Cancer

CDKi free base is a CDK inhibitor. CDKi free base induces morphological changes, DNA fragmentation, and cell death in vestibular schwannoma cells. CDKi free base downregulates pRb, EGF-R, PI3K, NF-κB, and Shh levels, while upregulating JNK, ASK1, Caspase 3, and p21, and induces PARP-1 cleavage. CDKi free base can be used in research related to vestibular schwannoma .
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Cat. No.: HY-P70578
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: AREG; AR; Prev. AREGB; schwannoma-Derived Growth Factor; Prev. SDGF; Amphiregulin B; CRDGF; Amphiregulin; Colorectum Cell-Derived Growth Factor
Species:  
Human
Source:  
E. coli
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Cat. No.: HY-P702502
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: AREG; AR; Prev. AREGB; schwannoma-Derived Growth Factor; Prev. SDGF; Amphiregulin B; CRDGF; Amphiregulin; Colorectum Cell-Derived Growth Factor
Species:  
Mouse
Source:  
E. coli
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Cat. No.: HY-P702502A
Purity:  ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: AREG; AR; Prev. AREGB; schwannoma-Derived Growth Factor; Prev. SDGF; Amphiregulin B; CRDGF; Amphiregulin; Colorectum Cell-Derived Growth Factor
Species:  
Mouse
Source:  
E. coli
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Cat. No.: HY-107662R
CAS No.: 34320-83-7
Research Areas:  

Infection Cancer

TCS PrP Inhibitor 13 (Standard) is the analytical standard of TCS PrP Inhibitor 13 (HY-107662). This product is intended for research and analytical applications. TCS PrP Inhibitor 13, an antiprion agent, is a cellular prion protein (PrPC) inhibitor. TCS PrP Inhibitor 13, as a protease-resistant form of prion protein (PrP-res) accumulation inhibitor, shows an IC50 value of 3 nM in both ScN2a and F3 cell lines. TCS PrP Inhibitor 13 induces Schwannoma cells apoptosis .
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Cat. No.: HY-L188
2,134 compounds

Although brain cancer only accounts for 2% of all tumors, it has a poor prognosis, high mortality and high recurrence rate. Brain cancer can be divided into primary brain cancer and secondary brain cancer. According to the location of the cancer, brain cancer can also be divided into: brain glioma, pituitary adenoma, schwannoma, craniopharyngioma, meningioma and so on. Glioma is the most common primary brain tumor, accounting for about 1/3 of all brain tumors. At present, brain cancer lacks precision targeted therapeutic drugs, and there is still a great clinical demand that has not been met. With the continuous development of high-throughput screening technology, it may be able to help develop effective anti-brain cancer drugs by screening compounds targeting PKC, PD-1, c-Met, PARP, etc targets.

MCE designs a unique collection of 2,134 small molecules with definite or potential anti-brain cancer activity, which is an important tool for studying the pathological mechanism of brain cancer and developing drugs for brain cancer.

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