Pyrroler
Aromatiske organiske heterocykliske forbindelser, der består af en femleddet ring med fire carbonatomer og et nitrogenatom, der danner en aminfunktionel gruppe.
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AZ PFKFB3 26, MedChemExpress
MedChemExpress AZ PFKFB3 26 is a potent and selective inhibitor of the metabolic kinase PFKFB3 with an IC50 of 23 nM. AZ PFKFB3 26 inhibits PFKFB1 and PFKFB2 with IC50s of 2.06 and 0.384 μM, respectively.
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Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Kemisk navn eller materiale | AZ PFKFB3 26 |
|---|---|
| Formel vægt | 402.49 |
| Opløselighedsinformation | DMSO : 5 mg/mL (12.42 mM; ultrasonic and adjust pH to 3 with HCl) |
| Procent renhed | 98.38% |
| Fysisk form | Solid |
| Farve | Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 402.49 |
| CAS | 1704740-52-2 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C([C@H]1NCCC1)NC2=CC=C(OC3=CC4=C(N(CC(C)C)C=C4C#N)C=C3)C=C2 |
| Renhedsgrad noter | Research |
| Molekylær formel | C24H26N4O2 |
| Til brug med (applikation) | Cancer-Kinase/protease |
Trilaciclib hydrochloride, MedChemExpress
MedChemExpress Trilaciclib hydrochloride (G1T28 hydrochloride) is a CDK4/6 inhibitor with IC50s of 1 nM and 4 nM for CDK4 and CDK6, respectively.
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Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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| Kemisk navn eller materiale | Trilaciclib hydrochloride |
|---|---|
| Formel vægt | 519.47 |
| Opløselighedsinformation | H2O : 25.64 mg/mL (49.36 mM; ultrasonic and adjust pH to 2 with HCl) ∣DMSO : 1.1 mg/mL (2.12 mM; Need ultrasonic) |
| Procent renhed | 98.2% |
| Fysisk form | Solid |
| Farve | Yellow |
| Grad | Research |
| Anbefalet opbevaring | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| Molekylvægt (g/mol) | 519.47 |
| CAS | 1977495-97-8 |
| Synonym | G1T28 hydrochloride |
| Holdbarhed | 4°C, sealed storage, away from moisture∣In solvent : -80°C, 6 months∣-20°C, 1 month (sealed storage, away from moisture) |
| SMIL | O=C1C2=CC3=CN=C(NC4=CC=C(N5CCN(C)CC5)C=N4)N=C3N2C6(CCCCC6)CN1.[H]Cl.[H]Cl |
| Renhedsgrad noter | Research |
| Molekylær formel | C24H32Cl2N8O |
| Til brug med (applikation) | Cancer-Kinase/protease |
Indoximod, MedChemExpress
MedChemExpress Indoximod (1-Methyl-D-tryptophan) is an orally active indoleamine 2,3-dioxygenase (IDO) pathway inhibitor. Indoximod acts as a Trp mimetic in regulating mTOR. Indoximod is an immunometabolic adjuvant used for the research of cancer.
Encompass Procurement Services
Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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Non-distribution item offered as a customer accommodation; additional freight charges may apply.
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