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Filtered Search Results
Medchemexpress LLC PSB-603 | 1092351-10-4 | 99.4% | 529.01 g/mol | C24H25ClN6O4S | 25 MG
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PSB-603 (CAS 1092351-10-4) is a potent, highly selective adenosine A2B receptor antagonist used in pharmacological research to block A2B-mediated signaling and investigate inflammatory responses. It exhibits subnanomolar affinity for A2B (Ki = 0.553 nM) and shows minimal activity at other adenosine receptor subtypes.
- Potent A2B antagonist with Ki = 0.553 nM.
- High purity (99.4%) as supplied.
- Molecular formula C24H25ClN6O4S; molecular weight 529.01 g/mol.
- Solid powder suitable for in vitro and in vivo studies.
- Storage recommendations: powder at -20°C (long term) or 4°C (short term); solutions at -80°C.
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eMolecules 51417-51-7 | 7-Bromoindole | Combi-Blocks | MFCD00799492 | 196.047 | C8H6BrN | 97.000 | Brc1cccc2cc[nH]c12 | 1g | 117535033
7-Bromoindole | Combi-Blocks | 51417-51-7 | MFCD00799492 | 196.047 | C8H6BrN | 97.000 | Brc1cccc2cc[nH]c12 | 1g | 117535033
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eMolecules 1373273-48-3 | 1-Boc-1H-pyrrolo[2,3-c]pyridin-2-ylboronic acid | J&W PharmLab LLC262.070 | C12H15BN2O4 | 96.000 | CC(C)(C)OC(=O)n1c(cc2ccncc12)B(O)O | 250mg | 794067006
1-Boc-1H-pyrrolo[2,3-c]pyridin-2-ylboronic acid | J&W PharmLab LLC | 1373273-48-3262.070 | C12H15BN2O4 | 96.000 | CC(C)(C)OC(=O)n1c(cc2ccncc12)B(O)O | 250mg | 794067006
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eMolecules 93247-78-0 | Methyl 1H-indole-7-carboxylate | Apollo Scientific | MFCD00211064 | 175.187 | C10H9NO2 | 97.000 | COC(=O)c1cccc2cc[nH]c12 | 5g | 600854958
Methyl 1H-indole-7-carboxylate | Apollo Scientific | 93247-78-0 | MFCD00211064 | 175.187 | C10H9NO2 | 97.000 | COC(=O)c1cccc2cc[nH]c12 | 5g | 600854958
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eMolecules 588688-33-9 | Methyl 3-methyl-1H-indole-5-carboxylate | Combi-Blocks, Inc. | MFCD11975645 | 189.214 | C11H11NO2 | 95.000 | COC(=O)c1ccc2[nH]cc(C)c2c1 | 10g | 866384308
Methyl 3-methyl-1H-indole-5-carboxylate | Combi-Blocks, Inc. | 588688-33-9 | MFCD11975645 | 189.214 | C11H11NO2 | 95.000 | COC(=O)c1ccc2[nH]cc(C)c2c1 | 10g | 866384308
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eMolecules 6160-65-2 | 1,1'-CARBONOTHIOYLBIS-1H-IMIDAZOLE | AstaTech | MFCD00005289 | 178.210 | C7H6N4S | 95.000 | S=C(n1ccnc1)n1ccnc1 | 50g | 357550272
1,1'-CARBONOTHIOYLBIS-1H-IMIDAZOLE | AstaTech | 6160-65-2 | MFCD00005289 | 178.210 | C7H6N4S | 95.000 | S=C(n1ccnc1)n1ccnc1 | 50g | 357550272
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eMolecules 588688-33-9 | Methyl 3-methyl-1H-indole-5-carboxylate | Combi-Blocks | MFCD11975645 | 189.214 | C11H11NO2 | 95.000 | COC(=O)c1ccc2[nH]cc(C)c2c1 | 1g | 267186021
Methyl 3-methyl-1H-indole-5-carboxylate | Combi-Blocks | 588688-33-9 | MFCD11975645 | 189.214 | C11H11NO2 | 95.000 | COC(=O)c1ccc2[nH]cc(C)c2c1 | 1g | 267186021
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Medchemexpress LLC 4-hydroxy-9H-xanthen-9-one | 14686-63-6 | MFCD01313128 | 98.0% | 212.20 | C13H8O3 | 5mg
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4-Hydroxy-9h-xanthen-9-one is a natural product[1]
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Apexbio Technology LLC N-(3-pyridyl)-Indomethacin amide 261766-29-4 5mg
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N-3-pyridyl-Indomethacin amide is a small-molecule inhibitor targeting cyclooxygenase-2 (COX-2) It is designed to selectively inhibit the COX-2 isoform thereby modulating inflammatory responses mediated by this enzyme N-3-pyridyl-Indomethacin amide exerts its biological activity primarily through reversible inhibition of COX-2 In studies with recombinant human COX-2 N-3-pyridyl-Indomethacin amide demonstrates potent inhibition with an IC50 value of approximately 0 052 M Based on these pharmacological properties N-3-pyridyl-Indomethacin amide holds research potential in the investigation of COX-2-related pathways in inflammation pain and associated cellular signaling events
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Apexbio Technology LLC Indomethacin(Synonyms: Indocin, Indometacin, Indomethacine, Indocid, Indocine, Amuno, Chrono-Indocid, Elmetacin), 1g, CAS: 53-86-1.
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Indomethacin (CAS 53-86-1) is a nonsteroidal anti-inflammatory compound that inhibits cyclooxygenase enzymes Cox-1 and Cox-2 displaying preferential inhibition toward Cox-1 (IC50 230 nM) compared to Cox-2 (IC50 630 nM) Additionally it acts as an agonist of peroxisome proliferator-activated receptor gamma (PPAR ) a transcriptional regulator implicated in adipogenesis Indomethacin can also activate PPAR Furthermore studies indicate that indomethacin stabilizes cholesterol-rich nanoscale clusters enhancing membrane phase separation and potentially altering membrane-dependent signaling pathways This profile makes indomethacin useful for investigating inflammation-associated processes lipid metabolism and membrane signaling mechanisms
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eMolecules 460751-66-0 | (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromo-1H-indol-3-yl)propanoic acid | ChemScene | MFCD28166519 | 505.368 | C26H21BrN2O4 | 98.000 | OC(=O)[C@H](Cc1c[nH]c2ccc(Br)cc12)NC(=O)OCC1c2ccccc2-c2ccccc12 | 10g | 875350038
(S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-3-(5-bromo-1H-indol-3-yl)propanoic acid | ChemScene | 460751-66-0 | MFCD28166519 | 505.368 | C26H21BrN2O4 | 98.000 | OC(=O)[C@H](Cc1c[nH]c2ccc(Br)cc12)NC(=O)OCC1c2ccccc2-c2ccccc12 | 10g | 875350038
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eMolecules 122350-52-1 | (S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(benzyloxy)-5-oxopentanoic acid | ChemScene | MFCD00080272 | 459.498 | C27H25NO6 | 96.000 | OC(=O)CC[C@H](NC(=O)OCC1c2ccccc2-c2ccccc12)C(=O)OCc1ccccc1 | 25g | 572180709
(S)-4-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-5-(benzyloxy)-5-oxopentanoic acid | ChemScene | 122350-52-1 | MFCD00080272 | 459.498 | C27H25NO6 | 96.000 | OC(=O)CC[C@H](NC(=O)OCC1c2ccccc2-c2ccccc12)C(=O)OCc1ccccc1 | 25g | 572180709
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Aobchem AOBCHEM
5000906553 ETHYL 2- 9-ISOPROPYL-9H-CARBAZ
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Advanced Chemblocks Inc S-2-9H-FLUOREN-9-YL METHOXY 1G
NC3728012 S-2-9H-FLUOREN-9-YL METHOXY 1G
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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000404265 2S 5S -1- 9H-FLUO 1G
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