Pyrroles
Medchemexpress LLC Methyl 1H-pyrrole-2-carboxylate | 1193-62-0 | 99.98% | 125.13 | 25 G
Methyl 1H-pyrrole-2-carboxylate is a drug intermediate that can act as an acyl donor. It can be synthesized into a series of pyrrolidine derivatives through tranesterification reactions with various alcohols.
- Drug intermediate
- Can act as an acyl donor
- Can be synthesized into a series of pyrrolidine derivatives through tranesterification reactions with various alcohols
SHANGHAI CHEMHERE CO LTD 1H PYRROLE 2 5 DIONE 3 4 10MG
1H-Pyrrole-2,5-dione, 3-(4-bromophenyl)-4-hydroxy-, 10mg, 84863-94-5
![eMolecules 625-82-1 | 2,4-Dimethylpyrrole | AA Blocks LLC | MFCD00192088 | 95.145 | C6H9N | 0.000 | Cc1c[nH]c(C)c1 | 100g | 713326739](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000473680.jpg-250.jpg)
eMolecules 625-82-1 | 2,4-Dimethylpyrrole | AA Blocks LLC | MFCD00192088 | 95.145 | C6H9N | 0.000 | Cc1c[nH]c(C)c1 | 100g | 713326739
2,4-Dimethylpyrrole | AA Blocks LLC | 625-82-1 | MFCD00192088 | 95.145 | C6H9N | 0.000 | Cc1c[nH]c(C)c1 | 100g | 713326739
Medchemexpress LLC 1H-Pyrrole-2-carboxylic acid | 634-97-9 | 111.10 | 100 G
Pyrrole-2-carboxylic acid is a natural alkaloid found in the marine bacterium *Pelomonas puraquae sp. Nov*. It is a biological form of pyrrole that is commonly found in natural compounds and serves as a precursor for various pyrrole derivatives in biosynthetic processes.
- Natural alkaloid
- Biological form of pyrrole
- Precursor for pyrrole derivatives
- Exhibits antineuroinflammatory activity
eMolecules 25128-35-2 | 2,3-Dioxoindoline-7-Carboxylic Acid | AA Blocks LLC | MFCD00612492 | 191.142 | C9H5NO4 | 0.000 | OC(=O)c1cccc2C(=O)C(=O)Nc12 | 1g | 436021899
2,3-Dioxoindoline-7-Carboxylic Acid | AA Blocks LLC | 25128-35-2 | MFCD00612492 | 191.142 | C9H5NO4 | 0.000 | OC(=O)c1cccc2C(=O)C(=O)Nc12 | 1g | 436021899
eMolecules 25128-32-9 | 2,3-Dioxoindoline-5-Carboxylic Acid | AA Blocks LLC | MFCD00967204 | 191.142 | C9H5NO4 | 0.000 | OC(=O)c1ccc2NC(=O)C(=O)c2c1 | 1g | 436021900
2,3-Dioxoindoline-5-Carboxylic Acid | AA Blocks LLC | 25128-32-9 | MFCD00967204 | 191.142 | C9H5NO4 | 0.000 | OC(=O)c1ccc2NC(=O)C(=O)c2c1 | 1g | 436021900
Medchemexpress LLC Pyrrole-2-carboxylic acid | 634-97-9 | 111.10 | 5 G
Pyrrole-2-carboxylic acid is a natural alkaloid found in the marine bacterium *Pelomonas puraquae* sp. Nov. This biological form of pyrrole is frequently encountered in natural compounds.
- Acts as a precursor for various pyrrole derivatives
- Involved in biosynthetic pathways for clorobiocin, coumermycin A1, pyoluteorin, leupyrrins, and undecylprodigiosin
Medchemexpress LLC Pyrrole-2-carboxaldehyde | 1003-29-8 | >99.99% | C5H5NO | 5 G
Pyrrole-2-carboxaldehyde is a five-membered N-heterocyclic system containing a pyrrole group as a proton donor and a carbonyl group as a proton acceptor. It exhibits vibrational and electronic characteristics that establish its dimeric form in solid phase and monomeric form in solution phase.
- Solid appearance
- White to light brown color
- Molecular weight of 95.10
- Classified as pyrrole alkaloids
- Initial source from plants
- Store at 4°C, protected from light and under nitrogen
- Soluble in DMSO at 100 mg/mL (1051.52 mM)
![eMolecules 625-82-1 | 2,4-Dimethyl-1H-pyrrole | Ambeed | MFCD00192088 | 95.145 | C6H9N | 98.000 | Cc1c[nH]c(C)c1 | 10g | 525246779](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000474156.jpg-250.jpg)
eMolecules 625-82-1 | 2,4-Dimethyl-1H-pyrrole | Ambeed | MFCD00192088 | 95.145 | C6H9N | 98.000 | Cc1c[nH]c(C)c1 | 10g | 525246779
2,4-Dimethyl-1H-pyrrole | Ambeed | 625-82-1 | MFCD00192088 | 95.145 | C6H9N | 98.000 | Cc1c[nH]c(C)c1 | 10g | 525246779
![eMolecules 625-82-1 | 2,4-Dimethyl-1H-pyrrole | Apollo Scientific | MFCD00192088 | 95.145 | C6H9N | 98.000 | Cc1c[nH]c(C)c1 | 5g | 562530882](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000491286.jpg-250.jpg)
eMolecules 625-82-1 | 2,4-Dimethyl-1H-pyrrole | Apollo Scientific | MFCD00192088 | 95.145 | C6H9N | 98.000 | Cc1c[nH]c(C)c1 | 5g | 562530882
2,4-Dimethyl-1H-pyrrole | Apollo Scientific | 625-82-1 | MFCD00192088 | 95.145 | C6H9N | 98.000 | Cc1c[nH]c(C)c1 | 5g | 562530882
Medchemexpress LLC MDL-29951 | 130798-51-5 | 99.2% | 302.11 | 5 MG
MDL-29951 is a novel glycine antagonist of NMDA receptor activation, exhibiting a Ki of 0.14 μM for [3H]glycine binding both in vitro and in vivo. It is intended for research use only.
- Approximately 2000-fold selective for the glycine binding site over glutamate recognition sites.
- Inhibits human F16Bpase (IC50=2.5 μM), porcine kidney (IC50=1.0 μM), and rabbit liver (IC50=0.21 μM) isoforms of the enzyme.
- Promotes Ca2+ signaling responses and inhibits cyclic adenosine monophosphate (cAMP) accumulation in rat oligodendrocyte precursor cells.
- Exhibits GPCR-mediated signaling activities, including G protein-dependent activation of ERK1/2 and recruitment of β-arrestin.
Medchemexpress LLC Pyrrole-2-carboxylic acid | 634-97-9 | 111.10 | 50 G
Pyrrole-2-carboxylic acid is a natural alkaloid found in the marine bacterium *Pelomonas puraquae* sp. Nov. It is a biological form of pyrrole often present in natural compounds and serves as a precursor for various pyrrole derivatives such as clorobiocin, coumermycin A1, pyoluteorin, leupyrrins, and undecylprodigiosin in biosynthetic processes. This product is for research use only.
- Natural alkaloid found in marine bacterium *Pelomonas puraquae* sp. Nov.
- Biological form of pyrrole.
- Precursor for various pyrrole derivatives (clorobiocin, coumermycin A1, pyoluteorin, leupyrrins, undecylprodigiosin).
- For research use only.
Apexbio Technology LLC Pyrrole-2-carboxylic acid 634-97-9 500mg
Pyrrole-2-carboxylic acid (CAS 634-97-9) is a heterocyclic organic compound characterized by a carboxyl substituent at the 2-position of the pyrrole ring This molecule has been investigated in biomedical research as an inhibitor of certain enzymatic pathways involving pyrrole derivatives including roles in microbial metabolism and secondary metabolite biosynthesis Pyrrole-2-carboxylic acid is utilized in studies examining enzyme specificity metabolic pathway modulation and as a precursor in the synthesis of pharmacologically relevant molecules Its defined structure makes it a valuable tool for probing pyrrole-related biochemical mechanisms