11 Results for "

Calu-1

" in MedChemExpress (MCE) Product Catalog:
Products (11)

11 Results for "Calu-1" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-160699
CAS No.: 2543673-19-2
Target:  

ULK Ras Autophagy

Research Areas:  

Cancer

DCC-3116 is an orally active ULK1/2 inhibitor. DCC-3116 can inhibit autophagy in lung cancer cells by inhibiting KRAS G12C signaling, thereby inhibiting the proliferation of lung cancer cells and exerting anti-cancer effects [1].
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1
1 Cited Publications
Cat. No.: HY-18707
CAS No.: 1469337-95-8
Target:  

Ras Apoptosis

Research Areas:  

Cancer

K-Ras(G12C) inhibitor 12 is an irreversible inhibitor of K-Ras(G12C). K-Ras(G12C) inhibitor 12 can alter the nucleotide-binding preference of K-Ras and block its interaction with effector proteins. K-Ras(G12C) inhibitor 12 can reduce cell viability and induce apoptosis in lung cancer cell lines with G12C mutations. K-Ras(G12C) inhibitor 12 has anti-tumor activity [1].
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Cat. No.: HY-123242
CAS No.: 344900-92-1
Purity:  99.11%
Target:  

Farnesyl Transferase

Research Areas:  

Cancer

FTI-2153 is a potent and highly selective inhibitor of farnesyltransferase (FTase), with an IC50 of 1.4 nM. FTI-2153 is >3000-fold more potent at blocking H-Ras (IC50, 10 nM) than Rap1A processing. Anti-cancer activity [1].
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Cat. No.: HY-147185
CAS No.: 2247753-73-5
Purity:  98.70%
Research Areas:  

Cancer

PRMT7-IN-1 (Compound 14) is a PRMT7 inhibitor with an IC50 of 2.1 μM. PRMT7-IN-1 shows anticancer activity against different cancer cells [1].
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Cat. No.: HY-147636
CAS No.: 2508134-76-5
Target:  

Ras

Research Areas:  

Cancer

KRAS G12C inhibitor 55 (Compound 1) is a KRAS G12C inhibitor [1].
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Cat. No.: HY-123242A
CAS No.: 2820151-01-5
Purity:  99.11%
Target:  

Farnesyl Transferase

Research Areas:  

Cancer

FTI-2153 TFA is a potent and highly selective inhibitor of farnesyltransferase (FTase), with an IC50 of 1.4 nM. FTI-2153 TFA is >3000-fold more potent at blocking H-Ras (IC50, 10 nM) than Rap1A processing. Anti-cancer activity [1].
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Cat. No.: HY-N1107
CAS No.: 466-09-1
Synonyms: NSC 119993; NSC 277290; Odorigeni
Target:  

Others

Uzarigenin (NSC 119993; NSC 277290; Odorigeni) is a carnolide can be isolated from Pergularia tomentosa and exhibits antiproliferative activity. Uzarigenin resists the proliferation of PC3 cells, HeLa cells, Calu-1 cells, MCF-7 cells and U251MG cells, with IC50 values of 0.3 μM, 3.0 μM, 8.0 μM, 6.0 μM and 6.0 μM respectively [1].
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Cat. No.: HY-111207
CAS No.: 883561-04-4
Purity:  99.94%
Target:  

CDK Apoptosis

Research Areas:  

Cancer

CA224 (Compound 1) is a selective and orally active Cdk4–cyclin D1 inhibitor with an IC50 of 6.2 µM. CA224 induces cell apoptosis and shows antitumor activity [1].
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Cat. No.: HY-N18310
CAS No.: 275365-36-1
Robustaflavone 4′-methyl ether is a biflavonoid compound that can be isolated from the whole plant of Selaginella gracillima. Robustaflavone 4′-methyl ether inhibits the growth of cancer cells. Robustaflavone 4′-methyl ether can be used in the research of EBV-transformed B-cell carcinoma and lung cancer [1].
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Cat. No.: HY-184434
CAS No.: 3064280-41-4
Research Areas:  

Cancer

PRMT5-IN-57 is an orally active andselective MTA-cooperative PRMT5 inhibitor, with an IC50 of 8.39 nM against PRMT5/MTA complex. PRMT5-IN-57 exhibits potent and selective antiproliferative activity against MTAP-null cancer cells. PRMT5-IN-57 demonstrates significant in vivo antitumor efficacy in an HCT116 MTAP-/- CDX model. PRMT5-IN-57 can be used for the research of MTAP-deleted cancers [1].
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Cat. No.: HY-184244
CAS No.: 3094094-17-1
Synonyms: CAS-13312-010
Target:  

Deubiquitinase

Research Areas:  

Cancer

CAS-010 (CAS-13312-010) is a potent and selective USP28 inhibitor with an IC50 of 2.2 nM against full-length USP28. CAS-010 acts as a ubiquitin-competitive inhibitor and shows higher selectivity over USP25 (IC50 = 51 nM) and other USP family members, disrupting the 53BP1-USP28 interaction and suppressing p53-dependent transcription of CDKN1A (p21), MDM2, and BAX. CAS-010 can be used for studying USP28-mediated DNA damage response and p53 signaling in cancer-related research [1].
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