74 Results for "

Squalene

" in MedChemExpress (MCE) Product Catalog:
Products (74)

74 Results for "Squalene" in MCE Product Catalog:

3
3 Cited Publications
Cat. No.: HY-N1214
CAS No.: 111-02-4
Synonyms: Super Squalene; trans-Squalene; AddaVax
Squalene (Super Squalene) is an intermediate product in the synthesis of cholesterol, and shows several pharmacological properties such as hypolipidemic, hepatoprotective, antiatherosclerotic, cardioprotective, antioxidant, and antitumour activity .
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29
29 Publications Verification
Cat. No.: HY-103087
CAS No.: 1083162-61-1
Purity:  98.03%
Target:  

Ferroptosis

Research Areas:  

Others

FIN56 is a specific inducer of ferroptosis. FIN56 induces ferroptosis by inducing degradation of GPX4. FIN56 also binds to and activates squalene synthase .
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19
19 Cited Publications
Cat. No.: HY-17395A
CAS No.: 91161-71-6
Synonyms: TDT 067
Research Areas:  

Infection

Terbinafine (TDT 067) is an orally active and potent antifungal agent. Terbinafine is a potent non-competitive inhibitor of squalene epoxidase from Candida, with a Ki of 30 nM. Terbinafine also shows antibacterial activity against certain Gram-positive and Gram-negative bacteria . Terbinafine is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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19
19 Cited Publications
Cat. No.: HY-17395
CAS No.: 78628-80-5
Synonyms: TDT 067 hydrochloride
Research Areas:  

Infection

Terbinafine hydrochloride (TDT 067 hydrochloride) is an orally active and potent antifungal agent. Terbinafine hydrochloride is a potent non-competitive inhibitor of squalene epoxidase from Candida, with a Ki of 30 nM. Terbinafine hydrochloride also shows antibacterial activity against certain Gram-positive and Gram-negative bacteria . Terbinafine hydrochloride is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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16
16 Cited Publications
Cat. No.: HY-16343
CAS No.: 131060-14-5
Target:  

COX

Research Areas:  

Metabolic Disease

NB-598 is a potent and competitive inhibitor of squalene epoxidase (SE), and suppresses triglyceride biosynthesis through the farnesol pathway. NB-598 is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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16
16 Cited Publications
Cat. No.: HY-16343C
CAS No.: 155294-62-5
Target:  

COX

Research Areas:  

Metabolic Disease

NB-598 Maleate is a potent and competitive inhibitor of squalene epoxidase (SE), and suppresses triglyceride biosynthesis through the farnesol pathway. NB-598 (Maleate) is a click chemistry reagent, it contains an Alkyne group and can undergo copper-catalyzed azide-alkyne cycloaddition (CuAAc) with molecules containing Azide groups.
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6
6 Cited Publications
Cat. No.: HY-100313A
CAS No.: 182959-33-7
Purity:  98.23%
Research Areas:  

Infection Metabolic Disease

YM-53601, a squalene synthase inhibitor, reduces plasma cholesterol and triglyceride levels in vivo . YM-53601 inhibits squalene synthase derived from human hepatoma cells with an IC50 of 79 nM. Lipid-lowering agent . YM-53601 is also an inhibitor of farnesyl-diphosphate farnesyltransferase 1 (FDFT1) enzyme activity and abrogates HCV propagation .
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2
2 Cited Publications
Cat. No.: HY-100303A
CAS No.: 204067-52-7
Purity:  98.76%
Research Areas:  

Metabolic Disease

FR194738 is a squalene epoxidase inhibitor. FR194738 inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM.
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2
2 Cited Publications
Cat. No.: HY-100303
CAS No.: 204067-45-8
Purity:  99.84%
Research Areas:  

Metabolic Disease

FR194738 free base is a squalene epoxidase inhibitor. FR194738 inhibits squalene epoxidase activity in HepG2 cell homogenates with an IC50 of 9.8 nM.
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1
1 Cited Publications
Cat. No.: HY-16274
CAS No.: 189060-13-7
Synonyms: TAK-475
Target:  

Farnesyl Transferase

Research Areas:  

Metabolic Disease

Lapaquistat acetate (TAK-475) is a squalene synthase inhibitor, blocking the conversion of farnesyl diphosphate (FPP) to squalene in the cholesterol biosynthesis pathway . Lapaquistat acetate is effective at lowering low-density lipoprotein cholesterol, but it might cause liver damage. Lapaquistat acetate is used for hypercholesterolemia and mevalonate kinase deficiency (MKD) research .
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1
1 Cited Publications
Cat. No.: HY-17396
CAS No.: 101827-46-7
Synonyms: KP363 Hydrochloride
Target:  

Fungal Antibiotic

Research Areas:  

Infection

Butenafine Hydrochloride (KP363 Hydrochloride) is a synthetic benzylamine antifungal, works by inhibiting the synthesis of sterols by inhibiting squalene epoxidase.
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1
1 Cited Publications
Cat. No.: HY-W015635
CAS No.: 2179-57-9
Category:  

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