44 Results for "

DHPS

" in MedChemExpress (MCE) Product Catalog:
Products (44)

44 Results for "DHPS" in MCE Product Catalog:

8
8 Publications Verification
Cat. No.: HY-108314A
CAS No.: 150417-90-6
Purity:  ≥98.0%
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

GC7 Sulfate is a deoxyhypusine synthase (DHPS) inhibitor.
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8
8 Publications Verification
Cat. No.: HY-B0273
CAS No.: 68-35-9
Research Areas:  

Infection

Sulfadiazine is an orally active sulfonamide antibiotic. Sulfadiazine competitively inhibits p-aminobenzoic acid in the folic-acid-metabolism cycle, inhibiting multiplication of most Gram-positive and many Gram-negative bacteria. Sulfadiazine persists in soil long-term, and exerts selective pressure for sulfonamide-resistant microbial populations. Sulfadiazine targets Toxoplasma gondii DHPS enzyme. Sulfadiazine can be used for the research of congenital toxoplasmosis and bacterial infection .
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8
8 Publications Verification
Cat. No.: HY-B0273A
CAS No.: 547-32-0
Research Areas:  

Infection

Sulfadiazine sodium is an orally active sulfonamide antibiotic. Sulfadiazine sodium competitively inhibits p-aminobenzoic acid in the folic-acid-metabolism cycle, inhibiting multiplication of most Gram-positive and many Gram-negative bacteria. Sulfadiazine sodium persists in soil long-term, and exerts selective pressure for sulfonamide-resistant microbial populations. Sulfadiazine sodium targets Toxoplasma gondii DHPS enzyme. Sulfadiazine sodium can be used for the research of congenital toxoplasmosis and bacterial infection .
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8
8 Publications Verification
Cat. No.: HY-B0273B
CAS No.: 68-35-9
Research Areas:  

Infection

Sulfadiazine 100 µg/mL in methanol is an orally active sulfonamide antibiotic. Sulfadiazine 100 µg/mL in methanol competitively inhibits p-aminobenzoic acid in the folic-acid-metabolism cycle, inhibiting multiplication of most Gram-positive and many Gram-negative bacteria. Sulfadiazine 100 µg/mL in methanol persists in soil long-term, and exerts selective pressure for sulfonamide-resistant microbial populations. Sulfadiazine 100 µg/mL in methanol targets Toxoplasma gondii DHPS enzyme. Sulfadiazine 100 µg/mL in methanol can be used for the research of congenital toxoplasmosis and bacterial infection .
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2
2 Cited Publications
Cat. No.: HY-B0212
CAS No.: 144-83-2
Target:  

Bacterial Antibiotic

Research Areas:  

Infection Inflammation/Immunology

Sulfapyridine, a major metabolite of Sulfasalazine, is a sulfonamide antibiotic agent. Sulfapyridine inhibits recombinant P. carinii dihydropteroate synthetase (DHPS) with an IC50 of 0.18 μM. Sulfapyridine has antibacterial, anti-inflammatory and anti-rheumatic activities .
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2
2 Cited Publications
Cat. No.: HY-135218A
CAS No.: 19350-66-4
Purity:  99.65%
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

AV-153 free base, a 1,4-dihydropyridine (1,4-DHP) derivative, is an antimutagenic. AV-153 free base intercalates to DNA in a single strand break and reduces DNA damage, stimulates DNA repair in human cells in vitro. AV-153 free base interacts with thymine and cytosine and has an influence on poly(ADP)ribosylation. AV-153 free base has anti-cancer activity .
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1
1 Cited Publications
Cat. No.: HY-115712
CAS No.: 2643300-54-1
Purity:  99.78%
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

DHPS-IN-1, with the best DHPS inhibitory potency (IC50 = 0.014 μM), exhibits excellent inhibition against melanoma cells.
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1
1 Cited Publications
Cat. No.: HY-P70038
Purity:  ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: rHuDeoxyhypusine synthase/DHS, His; Deoxyhypusine Synthase; DHS; DHPS; DS
Species:  
Source:  
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Cat. No.: HY-W011231
CAS No.: 74936-72-4
Target:  

Calcium Channel

Research Areas:  

Cardiovascular Disease

DHP-050 is a Felodipine (HY-B0309) analog. DHP-050 can be used to study the structure-activity relationship of 1,4-dihydropyridine (DHP) compounds .
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Cat. No.: HY-161027
CAS No.: 1186292-00-1
Research Areas:  

Cancer

DHP-B is an Ecolignan-type compound and covalent, selective CPT1A inhibitor with a Kd of 1.62 μM. DHP-B can be isolated from the plant Peperomia dindygulensis. DHP-B covalently binds to Cys96 of CPT1A, blocks FAO, and disrupts the mitochondrial CPT1A-VDAC1 interaction. DHP-B triggers Apoptosis. DHP-B exhibits anti-CRC activity .
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Cat. No.: HY-108314
CAS No.: 150333-69-0
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

GC7 Sulfate is a deoxyhypusine synthase (DHPS) inhibitor.
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Cat. No.: HY-126171
CAS No.: 34994-11-1
Target:  

Endogenous Metabolite

Research Areas:  

Others

Hypusine is a natural amino acid. The post-translational synthesis of hypusine is mainly catalyzed by deoxyhypusine synthase (DHPS) and deoxyhypusine hydroxylase (DOHH) .
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Cat. No.: HY-B0612DS1
CAS No.: 1189954-18-4
Lercanidipine-d3 (hydrochloride) is the deuterium labeled Lercanidipine. Lercanidipine is a lipophilic third-generation dihydropyridine-calcium channel blocker (DHP-CCB). Lercanidipine has long lasting antihypertensive action and reno-protective effect .
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Cat. No.: HY-B0212R
CAS No.: 144-83-2
Sulfapyridine (Standard) is the analytical standard of Sulfapyridine. This product is intended for research and analytical applications. Sulfapyridine, a major metabolite of Sulfasalazine, is a sulfonamide antibiotic agent. Sulfapyridine inhibits recombinant P. carinii dihydropteroate synthetase (DHPS) with an IC50 of 0.18 μM. Sulfapyridine has antibacterial, anti-inflammatory and anti-rheumatic activities .
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Cat. No.: HY-B0273S
CAS No.: 1020719-78-1
Sulfadiazine-d4 is a deuterium labeled Sulfadiazine (HY-B0273). Sulfadiazine is an orally active sulfonamide antibiotic. Sulfadiazine competitively inhibits p-aminobenzoic acid in the folic-acid-metabolism cycle, inhibiting multiplication of most Gram-positive and many Gram-negative bacteria. Sulfadiazine persists in soil long-term, and exerts selective pressure for sulfonamide-resistant microbial populations. Sulfadiazine targets Toxoplasma gondii DHPS enzyme. Sulfadiazine can be used for the research of congenital toxoplasmosis and bacterial infection .
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Cat. No.: HY-B0612AS
CAS No.: 1261397-71-0
Lercanidipine- 13C,d3 (hydrochloride) is the deuterium and 13C labeled Lercanidipine hydrochloride . Lercanidipine hydrochloride is a lipophilic third-generation dihydropyridine-calcium channel blocker (DHP-CCB). Lercanidipine hydrochloride has long lasting antihypertensive action and reno-protective effect .
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Cat. No.: HY-B0273R
CAS No.: 68-35-9
Research Areas:  

Infection

Sulfadiazine (Standard) is the analytical standard of Sulfadiazine (HY-B0273). This product is intended for research and analytical applications. Sulfadiazine is an orally active sulfonamide antibiotic. Sulfadiazine competitively inhibits p-aminobenzoic acid in the folic-acid-metabolism cycle, inhibiting multiplication of most Gram-positive and many Gram-negative bacteria. Sulfadiazine persists in soil long-term, and exerts selective pressure for sulfonamide-resistant microbial populations. Sulfadiazine targets Toxoplasma gondii DHPS enzyme. Sulfadiazine can be used for the research of congenital toxoplasmosis and bacterial infection .
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Cat. No.: HY-W761300
CAS No.: 2446913-96-6
Target:  

Ligands for E3 Ligase

Research Areas:  

Others

1-(4-Pip-Ph)-DHP-dione is an E3 ligase ligand. 1-(4-Pip-Ph)-DHP-dione can be used for synthesis of PROTAC HPK1 Degrader-2 (HY-162544) .
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Cat. No.: HY-147721
CAS No.: 2418026-70-5
Target:  

Bacterial

Research Areas:  

Infection

Dihydropteroate synthase-IN-1 (compound 5g) is a potent dihydropteroate synthase (DHPS) inhibitor. Dihydropteroate synthase-IN-1 shows antimicrobial activities and antifungal activity. Dihydropteroate synthase-IN-1 inhibits cytochromes P450. Dihydropteroate synthase-IN-1 can bu used as diagnostic radio imaging material .
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Cat. No.: HY-175828
Target:  

DNA/RNA Synthesis

Research Areas:  

Cancer

DHPS-IN-2 is an allosteric deoxyhypusine synthase (DHPS) inhibitor with an IC50 of 70 nM and a Kd of 26.4 μM. DHPS-IN-2 significantly suppresses melanoma cell migration and invasiveness in vitro and exhibits potent anti-tumor efficacy in an A375 cell zebrafish xenograft model. DHPS-IN-2 can be used for the study of melanoma .
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