Indoles and derivatives
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Filtered Search Results
2-Fluoro-9H-carbazole 98.0+%, TCI America™
CAS: 391-53-7 Molecular Formula: C12H8FN Molecular Weight (g/mol): 185.20 MDL Number: MFCD09033508 InChI Key: RQGSXFCTBTUNRR-UHFFFAOYSA-N PubChem CID: 11816279 IUPAC Name: 2-fluoro-9H-carbazole SMILES: FC1=CC2=C(C=C1)C1=C(N2)C=CC=C1
| PubChem CID | 11816279 |
|---|---|
| CAS | 391-53-7 |
| Molecular Weight (g/mol) | 185.20 |
| MDL Number | MFCD09033508 |
| SMILES | FC1=CC2=C(C=C1)C1=C(N2)C=CC=C1 |
| IUPAC Name | 2-fluoro-9H-carbazole |
| InChI Key | RQGSXFCTBTUNRR-UHFFFAOYSA-N |
| Molecular Formula | C12H8FN |
2-Bromo-9-(2-naphthyl)-9H-carbazole 98.0+%, TCI America™
CAS: 1427316-53-7 Molecular Formula: C22H14BrN Molecular Weight (g/mol): 372.265 MDL Number: MFCD26127422 InChI Key: PYHCFFLUGHKAPZ-UHFFFAOYSA-N PubChem CID: 71302478 IUPAC Name: 2-bromo-9-naphthalen-2-ylcarbazole SMILES: C1=CC=C2C=C(C=CC2=C1)N3C4=CC=CC=C4C5=C3C=C(C=C5)Br
| PubChem CID | 71302478 |
|---|---|
| CAS | 1427316-53-7 |
| Molecular Weight (g/mol) | 372.265 |
| MDL Number | MFCD26127422 |
| SMILES | C1=CC=C2C=C(C=CC2=C1)N3C4=CC=CC=C4C5=C3C=C(C=C5)Br |
| IUPAC Name | 2-bromo-9-naphthalen-2-ylcarbazole |
| InChI Key | PYHCFFLUGHKAPZ-UHFFFAOYSA-N |
| Molecular Formula | C22H14BrN |
Indomethacin 98.0+%, TCI America™
CAS: 53-86-1 Molecular Formula: C19H16ClNO4 Molecular Weight (g/mol): 357.79 MDL Number: MFCD00057095 InChI Key: CGIGDMFJXJATDK-UHFFFAOYSA-N Synonym: indomethacin,indometacin,indocin,indometacine,indomethacine,indocid,metindol,amuno,indomethazine,imbrilon PubChem CID: 3715 ChEBI: CHEBI:49662 IUPAC Name: 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetic acid SMILES: CC1=C(C2=C(N1C(=O)C3=CC=C(C=C3)Cl)C=CC(=C2)OC)CC(=O)O
| PubChem CID | 3715 |
|---|---|
| CAS | 53-86-1 |
| Molecular Weight (g/mol) | 357.79 |
| ChEBI | CHEBI:49662 |
| MDL Number | MFCD00057095 |
| SMILES | CC1=C(C2=C(N1C(=O)C3=CC=C(C=C3)Cl)C=CC(=C2)OC)CC(=O)O |
| Synonym | indomethacin,indometacin,indocin,indometacine,indomethacine,indocid,metindol,amuno,indomethazine,imbrilon |
| IUPAC Name | 2-[1-(4-chlorobenzoyl)-5-methoxy-2-methylindol-3-yl]acetic acid |
| InChI Key | CGIGDMFJXJATDK-UHFFFAOYSA-N |
| Molecular Formula | C19H16ClNO4 |
eMolecules Ambeed / 2356-Tetra(9H-carbazol-9-yl)terephthalonitrile / 100mg / 642081202 / A752563 / / 1416881-53-2 / MFCD28369266 / 788.914 / C56H32N6
Ambeed / 2356-Tetra(9H-carbazol-9-yl)terephthalonitrile / 100mg / 642081202 / A752563 / / 1416881-53-2 / MFCD28369266 / 788.914 / C56H32N6
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Medchemexpress LLC L-tryptophan, N-[2-(1H-indol-3-yl)acetyl]- | 57105-53-0 | MFCD18641983 | 99.9% | 361.39 g·mol⁻1 | C21H19N3O3 | 5 MG
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(S)-N-(1H-Indole-3-acetyl)tryptophan is a chiral tryptophan derivative supplied as a white to off-white solid for research use. It has been characterized by NMR and LCMS and is reported to weakly inhibit β-D-glucosidase, making it useful for biochemical and enzymology studies.
- High purity: 99.9% (LCMS).
- Well characterized by 1H NMR and LCMS.
- Defined optical rotation: +11.00° (methanol, 25°C).
- Molecular weight: 361.39 g·mol⁻1.
- Recommended storage: powder at -20°C for long term stability.
- Intended for research use only; not for human or diagnostic use.
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eMolecules Pharmablock / 4-amino-2-methyl-23-dihydro-1H-isoindol-1-one / 25mg / 551136413 / PBN20120693 / 0.000 / 682757-53-5 / MFCD19252207 / 162.192 / C9H10N2O
Pharmablock / 4-amino-2-methyl-23-dihydro-1H-isoindol-1-one / 25mg / 551136413 / PBN20120693 / 0.000 / 682757-53-5 / MFCD19252207 / 162.192 / C9H10N2O
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Sigma Aldrich Ethyl 4-oxo-1-piperidinecarboxylate
MilliporeSigma Sigma Organics products encompass a wide range of quality reagents, solvents, catalysts, and building blocks for organic synthesis. From benchtop discovery to process development and scale-up, Sigma Organics solutions are built to meet the needs of synthetic chemists.
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| CAS | 29976-53-2 |
|---|
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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Apexbio Technology LLC Indomethacin(Synonyms: Indocin, Indometacin, Indomethacine, Indocid, Indocine, Amuno, Chrono-Indocid, Elmetacin), 10mM (in 1mL DMSO), 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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Apexbio Technology LLC Indomethacin(Synonyms: Indocin, Indometacin, Indomethacine, Indocid, Indocine, Amuno, Chrono-Indocid, Elmetacin), 5g, 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
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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