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Thienopyridines

Organic heterocyclic compounds that consist of a thiophene ring fused to a pyridine ring.
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Search Within Results
Keyword Search:
106 – 120 of 184 results
106

eMolecules​ 2R 4S-1-FMOC-4-BOC-AMINO 1G

5000170292 2R 4S-1-FMOC-4-BOC-AMINO 1G

ENCOMPASS_PREFERRED
107

Cayman Chemical Pentacosanoic Acid methyl est
SDP

A long chain saturated, fatty acid; the methyl ester of the 25-carbon, fully saturated fatty acid pentacosanoic acid; designed to be used as a standard in total fatty acid analysis

ENCOMPASS_PREFERRED
108

Medchemexpress LLC Pyridin-4-ol | 25G
SDP

Pyridin-4-ol | 25G

ENCOMPASS_PREFERRED
109

eMolecules​ 3S-TETRAHYDROFURAN-3-AMI 25G

5000223728 3S-TETRAHYDROFURAN-3-AMI 25G

ENCOMPASS_PREFERRED
110

eMolecules​ 3 5-DICHLOROPYRIDAZIN-4-AMI 5G

5000217484 3 5-DICHLOROPYRIDAZIN-4-AMI 5G

ENCOMPASS_PREFERRED
111

Medchemexpress LLC MEDCHEMEXPRESS LLC
SDP

5000669297 HUMAN GIP3-30 AMI 50MG

ENCOMPASS_PREFERRED
112

Medchemexpress LLC AMI-1 free acid | 134-47-4 | 99.5% | 504.49 | 1 ML
SDP

AMI-1 free acid is a potent, cell-permeable, and reversible inhibitor of protein arginine N-methyltransferases (PRMTs), with IC50s of 8.8 μM for human PRMT1 and 3.0 μM for yeast-Hmt1p. It exerts its inhibitory effects on PRMTs by blocking peptide-substrate binding.

  • Potent, cell-permeable, and reversible inhibitor of PRMTs.
  • Inhibits type I PRMTs and type II PRMT5.
  • Specifically inhibits arginine methyltransferase activity, not lysine, and does not compete for the AdoMet binding site.
  • Inhibits methylation of GFP-Npl3 and cellular proteins.
  • Inhibits the cell viability of sarcoma in S180 and U2OS cells in a time- and dose-dependent manner in vitro.
  • Reduces S180 cell viability through the induction of cell apoptosis.
  • Inhibits S180 viability in vivo.
  • Downregulates PRMT5 and decreases levels of H4R3me2s and H3R8me2s in a tumor xenograft model.

ENCOMPASS_PREFERRED
113

eMolecules​ Pharmablock / 1H-pyrrolo[23-b]pyridine-5-carbaldehyde / 25mg / 599423997 / PB01422 / 0.000 / 849067-90-9 / MFCD08272241 / 146.149 / C8H6N2O

Pharmablock / 1H-pyrrolo[23-b]pyridine-5-carbaldehyde / 25mg / 599423997 / PB01422 / 0.000 / 849067-90-9 / MFCD08272241 / 146.149 / C8H6N2O

ENCOMPASS_PREFERRED
114

Medchemexpress LLC AMI-1 | 20324-87-2 | 98.0% | 548.45 | 25 MG
SDP

AMI-1 is a potent, cell-permeable, and reversible inhibitor of protein arginine N-methyltransferases (PRMTs), with IC50s of 8.8 μM for human PRMT1 and 3.0 μM for yeast-Hmt1p. It inhibits PRMTs by blocking peptide-substrate binding.

  • Potent, cell-permeable, and reversible inhibitor
  • Inhibits in vitro methylation reactions performed by PRMT1, -3, -4, -6, and Hmt1p
  • Inhibits both type I and type II PRMTs
  • Specifically inhibits arginine methyltransferase activity
  • Does not compete for the AdoMet binding site
  • Inhibits methylation of GFP-Npl3 and cellular proteins

ENCOMPASS_PREFERRED
115

Medchemexpress LLC MEDCHEMEXPRESS LLC
SDP

5000669312 HUMAN GIP3-30 AMI 25MG

ENCOMPASS_PREFERRED
116

eMolecules​ 2-OXASPIRO 3.3 HEPTAN-6-AM 25G

5000189629 2-OXASPIRO 3.3 HEPTAN-6-AM 25G

ENCOMPASS_PREFERRED
117

eMolecules​ 3 6-DICHLOROPYRIDAZIN-4-AMI 5G

5000159537 3 6-DICHLOROPYRIDAZIN-4-AMI 5G

ENCOMPASS_PREFERRED
118

eMolecules​ TERT-BUTYL N- 1R 3R-3-AMI 5G

5000163376 TERT-BUTYL N- 1R 3R-3-AMI 5G

ENCOMPASS_PREFERRED
119

eMolecules​ TERT-BUTYL N- 1R 3R-3-AMI 1G

5000164196 TERT-BUTYL N- 1R 3R-3-AMI 1G

ENCOMPASS_PREFERRED
120

Medchemexpress LLC N-Carbobenzyloxy-amino-L-alanine | 35761-26-3 | 238.24 | 25 G
SDP

N-Carbobenzyloxy-amino-L-alanine is an alanine derivative. Amino acids and their derivatives are used commercially as ergogenic supplements, influencing various physiological activities. This compound offers beneficial properties as an ergogenic dietary substance.

  • Alanine derivative
  • Used as an ergogenic supplement
  • Influences secretion of anabolic hormones
  • Enhances fuel supply during exercise
  • Improves mental performance under stress
  • Prevents exercise-induced muscle damage

ENCOMPASS_PREFERRED