Pyrazoles

Organic heterocyclic compounds that consists of a 5-membered ring of three carbon atoms and two adjacent nitrogen atoms with the formula: C₃H₃N₂H.

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331 – 345 of 1,831 results

331

Aobchem 3-(Thiophen-2-yl)-1H-pyrazole | ≥95% | CAS 19933-24-5 | C7H6N2S | 1g

3-(Thiophen-2-yl)-1H-pyrazole | ≥95% | CAS 19933-24-5 | C7H6N2S | 1g

Pricing & Availability

332

Aobchem 4-Chloro-1-ethyl-1H-pyrazole-5-carboxylic acid | ≥95% | CAS 400756-39-0 | C6H7ClN2O2 | 1g

4-Chloro-1-ethyl-1H-pyrazole-5-carboxylic acid | ≥95% | CAS 400756-39-0 | C6H7ClN2O2 | 1g

Pricing & Availability

333

eMolecules 1328893-17-9 | methyl 5-bromo-1H-pyrazole-3-carboxylate | Pharmablock | MFCD23701497 | 205.011 | C5H5BrN2O2 | 97.000 | COC(=O)c1cc(Br)[nH]n1 | 25g | 600902827

methyl 5-bromo-1H-pyrazole-3-carboxylate | Pharmablock | 1328893-17-9 | MFCD23701497 | 205.011 | C5H5BrN2O2 | 97.000 | COC(=O)c1cc(Br)[nH]n1 | 25g | 600902827

Pricing & Availability

334

Medchemexpress LLC RecO E.coli His-SU 50ug

RecO Protein, E. coli (His-SUMO) is a recombinant Escherichia coli DNA repair protein supplied as a lyophilized preparation with an N-terminal His-SUMO fusion tag. It is intended for research use in DNA recombination and repair studies; consult the Certificate of Analysis for lot-specific concentration and storage instructions.

Recombinant E. coli RecO with N-terminal His-SUMO tag for purification and detection.
Lyophilized powder for improved stability and long-term storage.
Approximate molecular weight 43.4 kDa for experimental planning.
Suitable for DNA repair and recombination studies.
Certificate of Analysis and SDS available for lot-specific details.

Pricing & Availability

335

eMolecules 68703-67-3 | ChemScene | 4-Amino-1H-pyrazole-3-carbonitrile | 100mg | 572243502 | CS-W019204 | MFCD00619110 | 108.104 | C4H4N4

ChemScene | 4-Amino-1H-pyrazole-3-carbonitrile | 100mg | 572243502 | CS-W019204 | 68703-67-3 | MFCD00619110 | 108.104 | C4H4N4

Pricing & Availability

336

Research Products International Corp Allopurinol 5 G

Allopurinol inhibits the enzyme xanthine oxidase, which is involved in the production of uric acid. Researchers may use allopurinol to manipulate uric acid levels in experimental settings, allowing them to study the metabolism and physiological effects of uric acid in various tissues and organs.

Allopurinol may be used in studies examining drug interactions or combination therapies. By understanding how allopurinol interacts with other medications or compounds, researchers can optimize treatment strategies and minimize potential adverse effects.

Allopurinol's mechanism of action extends beyond its inhibition of xanthine oxidase. Researchers may utilize allopurinol to probe the downstream effects of xanthine oxidase inhibition, including alterations in oxidative stress, inflammation, and purine metabolism pathways.