206 Results for "

second-generation

" in MedChemExpress (MCE) Product Catalog:
Products (206)

206 Results for "second-generation" in MCE Product Catalog:

6
6 Cited Publications
Cat. No.: HY-101212
CAS No.: 1070790-89-4
Purity:  99.50%
Synonyms: CYC065
Target:  

CDK

Research Areas:  

Cancer

Fadraciclib (CYC065) is a second-generation, orally available ATP-competitive inhibitor of CDK2/CDK9 kinases with IC50s of 5 and 26 nM, respectively .
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6
6 Cited Publications
Cat. No.: HY-B0656
CAS No.: 117976-89-3
Synonyms: LY307640
Rabeprazole (LY307640) is a second-generation proton pump inhibitor (PPI) that irreversibly inactivates gastric H +/K +-ATPase. Rabeprazole induces apoptosis. Rabeprazole acts as an uridine nucleoside ribohydrolase (UNH) inhibitor with an IC50 of 0.3 μM. Rabeprazole can be used for the research of gastric ulcerations and gastroesophageal reflux .
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6
6 Cited Publications
Cat. No.: HY-B0656A
CAS No.: 117976-90-6
Synonyms: LY307640 sodium
Rabeprazole sodium (LY307640 sodium) is a second-generation proton pump inhibitor (PPI) that irreversibly inactivates gastric H +/K +-ATPase. Rabeprazole sodium induces apoptosis. Rabeprazole sodium acts as an uridine nucleoside ribohydrolase (UNH) inhibitor with an IC50 of 0.3 μM. Rabeprazole sodium can be used for the research of gastric ulcerations and gastroesophageal reflux .
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6
6 Cited Publications
Cat. No.: HY-19948
CAS No.: 1236208-20-0
Synonyms: TRx0237 mesylate; Methylene blue leuco base mesylate
Leucomethylene blue (TRx0237) mesylate, an orally active second-generation tau protein aggregation inhibitor (Ki of 0.12 μM), could be used for the study of Alzheimer's Disease. Leucomethylene blue mesylate is a common reduced form of Methylene Blue, Methylene Blue is a member of the thiazine class of dyes .
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5
5 Cited Publications
Cat. No.: HY-15835
CAS No.: 1446182-94-0
Purity:  99.32%
Synonyms: GDC-0917
Target:  

IAP

Research Areas:  

Cancer

CUDC-427 is a potent second-generation pan-selective IAP antagonist, used for treatment of various cancers.
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4
4 Cited Publications
Cat. No.: HY-B0107
CAS No.: 55079-83-9
Synonyms: Ro 10-1670
Research Areas:  

Inflammation/Immunology Cancer

Acitretin (Ro 10-1670) is a second-generation, systemic retinoid that has been used in the treatment of psoriasis. Acitretin also can be used for the research of Alzheimer’s disease .
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4
4 Cited Publications
Cat. No.: HY-17404
CAS No.: 132203-70-4
Synonyms: FRC-8653
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

Cilnidipine is a long-acting, second-generation dihydropyridine Ca 2+-channel blocker on L and N-type Ca 2+ channel . Antihypertensive effects .
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4
4 Cited Publications
Cat. No.: HY-B0157
CAS No.: 34580-13-7
Synonyms: HC 20-511
Ketotifen (HC 20-511) is an orally active second-generation noncompetitive histamine 1 (H1) receptor blocker and mast cell stabilizer. Ketotifen can block 6-phosphogluconate dehydrogenase (PGD) in vitro. Ketotifen also has antiviral activity against SARS-CoV-2 and Influenza virus. Ketotifen can be used to the research of autoimmune encephalomyelitis (EAE) and asthma attack prevention .
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4
4 Cited Publications
Cat. No.: HY-B0157A
CAS No.: 34580-14-8
Synonyms: HC 20511 fumarate
Ketotifen (HC 20-511) fumarate is an orally active second-generation noncompetitive histamine 1 (H1) receptor blocker and mast cell stabilizer. Ketotifen fumarate can block 6-phosphogluconate dehydrogenase (PGD) in vitro. Ketotifen fumarate also has antiviral activity against SARS-CoV-2 and Influenza virus. Ketotifen fumarate can be used to the research of autoimmune encephalomyelitis (EAE) and asthma attack prevention .
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4
4 Cited Publications
Cat. No.: HY-100423
CAS No.: 1642300-52-4
Purity:  99.79%
Synonyms: KPT-8602
Target:  

CRM1

Research Areas:  

Cancer

Eltanexor (KPT-8602) is a second-generation, highly specific and orally active exportin-1 (XPO1) inhibitor with potent anti-leukemic activity. Eltanexor (KPT-8602) inhibits XPO1-dependent nuclear export (EC50=60.9 nM) by directly targeting XPO1. Eltanexor (KPT-8602) induces Caspase-dependent apoptosis in a panel of leukemic cell lines .
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4
4 Cited Publications
Cat. No.: HY-101126
CAS No.: 1361951-15-6
Purity:  99.96%
Synonyms: TP-3654
Research Areas:  

Cancer

Nuvisertib (TP-3654) is an orally active second-generation pan-PIM kinase inhibitor with Ki values of 5 nM, 239 nM, and 42 nM against PIM-1, PIM-2, and PIM-3, respectively. Nuvisertib inhibits JAK-independent inflammatory and survival signaling pathways, reduces the production of proinflammatory cytokines, restores apoptotic sensitivity, inhibits mTORC1, MYC, and TGF-β signaling pathways, and decreases the expression of fibrosis markers. Nuvisertib selectively impairs the transport function of ABCG2, resensitizes multidrug-resistant cancer cells to cytotoxic drugs, and overcomes JAK2 inhibitor resistance. Nuvisertib can be used in research related to myelofibrosis, renal cell carcinoma, multidrug-resistant cancer, advanced solid tumors, urothelial carcinoma, and prostate adenocarcinoma .
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4
4 Cited Publications
Cat. No.: HY-15994
CAS No.: 1316215-12-9
Synonyms: ACY241
Target:  

HDAC

Research Areas:  

Cancer

Citarinostat (ACY241) is a second generation potent, orally active and high-selective HDAC6 inhibitor with an IC50 of 2.6 nM (IC50s of 35 nM, 45 nM, 46 nM and 137 nM for HDAC1, HDAC2, HDAC3 and HDAC8, respectively). Citarinostat has anticancer effects .
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3
3 Cited Publications
Cat. No.: HY-17042
CAS No.: 83881-51-0
Cetirizine, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine, is a specific, orally active and long-acting histamine H1-receptor antagonist. Cetirizine marks antiallergic properties and inhibits eosinophil chemotaxis during the allergic response .
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3
3 Cited Publications
Cat. No.: HY-17042A
CAS No.: 83881-52-1
Synonyms: P071
Cetirizine dihydrochloride, a second-generation antihistamine and the carboxylated metabolite of hydroxyzine, is a specific, orally active and long-acting histamine H1-receptor antagonist. Cetirizine dihydrochloride marks antiallergic properties and inhibits eosinophil chemotaxis during the allergic response .
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3
3 Cited Publications
Cat. No.: HY-120056
CAS No.: 2172617-15-9
Purity:  99.66%
Research Areas:  

Inflammation/Immunology

YKL-06-061 is a potent, selective, second-generation salt-inducible kinase (SIK) inhibitor with IC50 values of 6.56 nM/1.77 nM/20.5 nM for SIK1/2/3, respectively .
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3
3 Cited Publications
Cat. No.: HY-13722
CAS No.: 149402-51-7
Purity:  99.74%
Synonyms: Photochlor
Research Areas:  

Cancer

HPPH (Photochlor) is a second generation photosensitizer, which acts as a photodynamic therapy (PDT) agent.
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3
3 Cited Publications
Cat. No.: HY-134990
CAS No.: 148471-91-4
Purity:  ≥95.0%
Target:  

Apoptosis

Research Areas:  

Cancer

Hematoporphyrin monomethyl ether, second generation of porphyrin-related photosensitizer, is characterized by its single form, high yield of singlet oxygen, high selectivity, and low toxicity, which has been widely used in the diagnosis and research of various tumors, including lung cancer, bladder cancer, and nevus flammeus and brain glioma .
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2
2 Cited Publications
Cat. No.: HY-129141
CAS No.: 2172617-16-0
Purity:  99.44%
Research Areas:  

Inflammation/Immunology

YKL-06-062 is a second-generation salt-inducible kinase (SIK) inhibitor with an IC50 of 2.12 nM/1.40 nM/2.86 nM for SIK1, SIK2 and SIK3, respectively .
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2
2 Cited Publications
Cat. No.: HY-76200S
CAS No.: 1217661-14-7
Synonyms: UK-109496-d3
Voriconazole-d3 is the deuterium labeled Voriconazole. Voriconazole (UK-109496) is a second-generation, broad-spectrum triazole antifungal agent that inhibits fungal ergosterol biosynthesis. Voriconazole exerts its antifungal activity by inhibition of 14-α-lanosterol demethylation, which is mediated by fungal cytochrome P450 enzymes .
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2
2 Cited Publications
Cat. No.: HY-108361
CAS No.: 1443437-74-8
Purity:  99.89%
Target:  

Ras

Research Areas:  

Inflammation/Immunology Cancer

CCG-203971 is a second-generation Rho/MRTF/SRF pathway inhibitor. CCG-203971 potently targets RhoA/C-activated SRE-luciferase (IC50 =6.4 μM). CCG-203971 inhibits PC-3 cell migration with an IC50 of 4.2 μM. Potential anti-metastasis Agent .
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