Pyrroler
Filtrerade sökresultat
5-Bromo-2-phenyl-7-azaindole, 97%, Thermo Scientific Chemicals
CAS: 953414-75-0 Molekylformel: C13H9BrN2 Molekylvikt (g/mol): 273.13 MDL-nummer: MFCD11109822 InChI-nyckel: QLKZJMXSXCDCCF-UHFFFAOYSA-N Synonym: 5-bromo-2-phenyl-1h-pyrrolo 2,3-b pyridine,5-bromo-2-phenyl-7-azaindole,1h-pyrrolo 2,3-b pyridine,5-bromo-2-phenyl,2-phenyl-5-bromo-1h-pyrrolo 2,3-b pyridine PubChem CID: 23643607 IUPAC-namn: 5-brom-2-fenyl-lH-pyrrolo[2,3-b]pyridin LEDER: BrC1=CN=C2NC(=CC2=C1)C1=CC=CC=C1
| Molekylformel | C13H9BrN2 |
|---|---|
| PubChem CID | 23643607 |
| MDL-nummer | MFCD11109822 |
| IUPAC-namn | 5-brom-2-fenyl-lH-pyrrolo[2,3-b]pyridin |
| CAS | 953414-75-0 |
| InChI-nyckel | QLKZJMXSXCDCCF-UHFFFAOYSA-N |
| LEDER | BrC1=CN=C2NC(=CC2=C1)C1=CC=CC=C1 |
| Molekylvikt (g/mol) | 273.13 |
| Synonym | 5-bromo-2-phenyl-1h-pyrrolo 2,3-b pyridine,5-bromo-2-phenyl-7-azaindole,1h-pyrrolo 2,3-b pyridine,5-bromo-2-phenyl,2-phenyl-5-bromo-1h-pyrrolo 2,3-b pyridine |
Pyrrole-3-carboxylic acid hydrate, 95%
CAS: 336100-46-0 Molekylformel: C5H5NO2 Molekylvikt (g/mol): 111.10 MDL-nummer: MFCD06201862 InChI-nyckel: DOYOPBSXEIZLRE-UHFFFAOYSA-N Synonym: pyrrole-3-carboxylic acid hydrate,1h-pyrrole-3-carboxylic acid hydrate,c5h5no2.h2o,1h-pyrrole-3-carboxylicacid, hydrate 1:? PubChem CID: 45076181 IUPAC-namn: 1H-pyrrol-3-karboxylsyra;hydrat LEDER: OC(=O)C1=CNC=C1
| Molekylformel | C5H5NO2 |
|---|---|
| PubChem CID | 45076181 |
| MDL-nummer | MFCD06201862 |
| IUPAC-namn | 1H-pyrrol-3-karboxylsyra;hydrat |
| CAS | 336100-46-0 |
| InChI-nyckel | DOYOPBSXEIZLRE-UHFFFAOYSA-N |
| LEDER | OC(=O)C1=CNC=C1 |
| Molekylvikt (g/mol) | 111.10 |
| Synonym | pyrrole-3-carboxylic acid hydrate,1h-pyrrole-3-carboxylic acid hydrate,c5h5no2.h2o,1h-pyrrole-3-carboxylicacid, hydrate 1:? |
Dirlotapide, MedChemExpress
MedChemExpress Dirlotapide (CP742033) is a gut-selective inhibitor of microsomal triglyceride transfer protein (MTP) that reliably produces weight loss in obese dogs.
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SB269652, MedChemExpress
MedChemExpress SB269652 is the first drug-like allosteric modulator of the dopamine D2 receptor (D2R); a new chemical probe that can differentiate D2R monomers from dimers or oligomers depending on the observed pharmacology.
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Vinburnine, MedChemExpress
MedChemExpress Vincamone is a vinca alkaloid and a metabolite of vincamine, is a vasodilator.
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Apyramide, MedChemExpress
MedChemExpress Apyramide is an anti-inflammatory agent (NSAID) and behaves as a prodrug of indomethacin (HY-14397). Indomethacin is a potent, blood-brain permeable and nonselective inhibitor of COX1 and COX2.
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| Molekylformel | C27H23ClN2O5 |
|---|---|
| Rekommenderad förvaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Formel vikt | 490.93 |
| Hållbarhet | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Anteckningar om renhetsgrad | Research |
| Fysisk form | Solid |
| Kvalitet | Research |
| Färg | White |
| CAS | 68483-33-0 |
| LEDER | O=C(OC1=CC=C(NC(C)=O)C=C1)CC2=C(C)N(C(C3=CC=C(Cl)C=C3)=O)C4=C2C=C(OC)C=C4 |
| Molekylvikt (g/mol) | 490.93 |
| Kemiskt namn eller material | Apyramide |
| Procent renhet | 99.06% |
| För användning med (applikation) | COVID-19-immunoregulation |
KW-8232 free base, MedChemExpress
MedChemExpress KW-8232 free base, an orally active anti-osteoporotic agent, and can reduces the biosynthesis of PGE2.
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ITX3, MedChemExpress
MedChemExpress ITX3 is a specific and nontoxic inhibitor of the TrioN (N-terminal GEF domain of the multidomain Trio protein) with IC50 of 76 uM; inhibits TrioN-stimulated RhoG exchange in vitro.
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| Molekylformel | C22H17N3OS |
|---|---|
| Rekommenderad förvaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Formel vikt | 371.45 |
| Hållbarhet | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Löslighetsinformation | DMSO : 2 mg/mL (5.38 mM; ultrasonic and warming and heat to 80°C) |
| Anteckningar om renhetsgrad | Research |
| Fysisk form | Solid |
| Kvalitet | Research |
| Färg | Light Green |
| CAS | 347323-96-0 |
| LEDER | O=C(/C1=C\C2=C(C)N(C(C)=C2)C3=CC=CC=C3)N4C(S1)=NC5=CC=CC=C45 |
| Molekylvikt (g/mol) | 371.45 |
| Kemiskt namn eller material | ITX3 |
| Procent renhet | 98.01% |
Nigakinone, MedChemExpress
MedChemExpress Nigakinone is one of the most abundant alkaloids responsible for the major pharmacological activities of Kumu.
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GSK2606414, MedChemExpress
MedChemExpress GSK2606414 is a cell-permeable and orally available protein kinase R-like endoplasmic reticulum (ER) kinase (PERK) inhibitor with an IC50 of 0.4 nM.
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| Molekylformel | C24H20F3N5O |
|---|---|
| Rekommenderad förvaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Formel vikt | 451.44 |
| Hållbarhet | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Hälsofara 1 | H302 |
| Löslighetsinformation | DMSO : ≥ 100 mg/mL (221.51 mM) |
| Anteckningar om renhetsgrad | Research |
| Fysisk form | Solid |
| Kvalitet | Research |
| Färg | White |
| CAS | 1337531-36-8 |
| LEDER | NC1=C2C(N(C)C=C2C3=CC4=C(N(C(CC5=CC=CC(C(F)(F)F)=C5)=O)CC4)C=C3)=NC=N1 |
| Molekylvikt (g/mol) | 451.44 |
| Kemiskt namn eller material | GSK2606414 |
| Procent renhet | 98.59% |
| För användning med (applikation) | Cancer-Kinase/protease |
EHop-016, MedChemExpress
MedChemExpress EHop-016 is a potent and selective Rac GTPase Rac1 and Rac3 inhibitor. EHop-016 inhibits Rac1 activity with an IC50 of 1.1 μM in MDA-MB-435 cells. EHop-016 inhibits Vav2 interaction with Rac, Rac-activated PAK1, lamellipodia formation, and cell migration.
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| Molekylformel | C25H30N6O |
|---|---|
| Rekommenderad förvaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Formel vikt | 430.55 |
| Hållbarhet | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Löslighetsinformation | DMSO : ≥ 32 mg/mL (74.32 mM) |
| Anteckningar om renhetsgrad | Research |
| Fysisk form | Solid |
| Kvalitet | Research |
| Färg | Pink |
| CAS | 1380432-32-5 |
| LEDER | CCN1C2=C(C3=C1C=CC=C3)C=C(NC4=NC(NCCCN5CCOCC5)=NC=C4)C=C2 |
| Molekylvikt (g/mol) | 430.55 |
| Kemiskt namn eller material | EHop-016 |
| Procent renhet | 99.43% |
| För användning med (applikation) | Cancer-Kinase/protease |
PBOX 6, MedChemExpress
MedChemExpress PBOX 6 is a pyrrolo-1,5-benzoxazepine (PBOX) compound, acts as a microtubule-depolymerizing agent and an apoptotic agent.
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| Molekylformel | C25H20N2O3 |
|---|---|
| Rekommenderad förvaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Formel vikt | 396.44 |
| Hållbarhet | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Löslighetsinformation | DMSO : 33.33 mg/mL (84.07 mM; Need ultrasonic) |
| Anteckningar om renhetsgrad | Research |
| Fysisk form | Solid |
| Kvalitet | Research |
| Färg | White |
| CAS | 290814-68-5 |
| LEDER | O=C(OC1=C(C2=C3C=CC=CC3=CC=C2)OC4=CC=CC=C4N5C1=CC=C5)N(C)C |
| Molekylvikt (g/mol) | 396.44 |
| Kemiskt namn eller material | PBOX 6 |
| Procent renhet | 98.0% |
| För användning med (applikation) | Cancer-programmed cell death |
UNC2025, MedChemExpress
MedChemExpress UNC2025 is a potent, ATP-competitive and highly orally active Mer/Flt3 inhibitor with IC50 values of 0.74 nM and 0.8 nM, respectively. UNC2025 is >45-fold selectivity for MERTK relative to Axl (IC50= 122 nM; Ki = 13.3 nM). UNC2025 exhibits an excellent PK properties, and can be used for the investigation of acute leukemia.
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| Molekylformel | C28H40N6O |
|---|---|
| Rekommenderad förvaring | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Formel vikt | 476.66 |
| Hållbarhet | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| Löslighetsinformation | DMSO : 33.33 mg/mL (69.92 mM; Need ultrasonic and warming) |
| Anteckningar om renhetsgrad | Research |
| Fysisk form | Solid |
| Kvalitet | Research |
| Färg | White |
| CAS | 1429881-91-3 |
| LEDER | CN1CCN(CC2=CC=C(C3=CN([C@@H]4CC[C@@H](O)CC4)C5=NC(NCCCC)=NC=C53)C=C2)CC1 |
| Molekylvikt (g/mol) | 476.66 |
| Kemiskt namn eller material | UNC2025 |
| Procent renhet | 96.86% |
| För användning med (applikation) | Cancer-Kinase/protease |