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Filtrerede søgeresultater
PCI-34051, MedChemExpress
MedChemExpress PCI-34051 is a potent and selective HDAC8 inhibitor with IC50 of 10 nM, with >200-fold selectivity over the other HDAC isoforms.
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| Kemisk navn eller materiale | PCI-34051 |
|---|---|
| Formel vægt | 296.32 |
| Opløselighedsinformation | DMSO : ≥ 30 mg/mL (101.24 mM) |
| Procent renhed | 97.28% |
| Fysisk form | Solid |
| Farve | Off-White |
| 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) | 296.32 |
| CAS | 950762-95-5 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | COC(C=C1)=CC=C1CN2C3=CC(C(NO)=O)=CC=C3C=C2 |
| Renhedsgrad noter | Research |
| Molekylær formel | C17H16N2O3 |
| Til brug med (applikation) | Cancer-programmed cell death |
Vinburnine, MedChemExpress
MedChemExpress Vincamone is a vinca alkaloid and a metabolite of vincamine, is a vasodilator.
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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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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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| Kemisk navn eller materiale | Apyramide |
|---|---|
| Formel vægt | 490.93 |
| Procent renhed | 99.06% |
| Fysisk form | Solid |
| Farve | White |
| 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) | 490.93 |
| CAS | 68483-33-0 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | 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 |
| Renhedsgrad noter | Research |
| Molekylær formel | C27H23ClN2O5 |
| Til brug med (applikation) | COVID-19-immunoregulation |
Oncrasin-1, MedChemExpress
MedChemExpress Oncrasin-1 is a potent and effective anticancer inhibitor that kills various human lung cancer cells with K-Ras mutations at low or submicromolar concentrations; also led to abnormal aggregation of PKCι in nucleus of sensitive cells but not in resistant cells.
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| Kemisk navn eller materiale | Oncrasin-1 |
|---|---|
| Formel vægt | 269.73 |
| Opløselighedsinformation | DMSO : ≥ 43 mg/mL (159.42 mM) |
| Procent renhed | 98.28% |
| Fysisk form | Solid |
| Farve | Earth 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) | 269.73 |
| CAS | 75629-57-1 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=CC1=CN(CC(C=C2)=CC=C2Cl)C3=CC=CC=C31 |
| Renhedsgrad noter | Research |
| Molekylær formel | C16H12ClNO |
| Til brug med (applikation) | Cancer-Kinase/protease |
5-Iodotubercidin, MedChemExpress
MedChemExpress 5-Iodotubercidin (NSC 113939), an ATP mimetic, is a potent adenosine kinase inhibitor with an IC50 of 26 nM. 5-Iodotubercidin (NSC 113939) initiates glycogen synthesis in isolated hepatocytes by causing inactivation of phosphorylase and activation of glycogen synthase. 5-Iodotubercidin (NSC 113939) also inhibits CK1, insulin receptor tyrosine kinase, phosphorylase kinase, PKA, CK2, PKC and Haspin.
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| Kemisk navn eller materiale | 5-Iodotubercidin |
|---|---|
| Sundhedsfare 1 | H315∣H319∣H335 |
| Formel vægt | 392.15 |
| Opløselighedsinformation | DMSO : ≥ 49 mg/mL (124.95 mM) |
| Procent renhed | 95.0% |
| Fysisk form | Solid |
| Farve | Earth 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) | 392.15 |
| CAS | 24386-93-4 |
| Synonym | NSC 113939 5-ITu |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | NC1=C2C(N([C@H]3[C@H](O)[C@H](O)[C@@H](CO)O3)C=C2I)=NC=N1 |
| Renhedsgrad noter | Research |
| Molekylær formel | C11H13IN4O4 |
| Til brug med (applikation) | Cancer-Kinase/protease |
Metergoline, MedChemExpress
MedChemExpress Metergoline is a serotonin (5-HT) receptor and dopamine receptors antagonist, with pKis of 8.64, 8.75 and 8.75 for 5-HT2A, 5-HT2B and 5-HT2C, respectively. Metergoline is a high-affinity ligand for the h5-HT7 receptor, with a Ki of 16 nM. Metergoline is also a reversible neural Na+ channels inhibitor. Metergoline is commonly used for the research of seasonal affective disorder, prolactin hormone regulation.
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| Kemisk navn eller materiale | Metergoline |
|---|---|
| Sundhedsfare 1 | H302∣H312∣H332 |
| Formel vægt | 403.52 |
| Opløselighedsinformation | DMSO : 125 mg/mL (309.77 mM; Need ultrasonic) |
| Procent renhed | 98.62% |
| Fysisk form | Solid |
| Farve | White |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 403.52 |
| CAS | 17692-51-2 |
| Holdbarhed | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(OCC1=CC=CC=C1)NC[C@H](C[C@@]23[H])CN(C)[C@]2([H])CC4=CN(C)C5=CC=CC3=C54 |
| Renhedsgrad noter | Research |
| Molekylær formel | C25H29N3O2 |
| Til brug med (applikation) | Neuroscience-Neuromodulation |
(R)-Ketorolac, MedChemExpress
MedChemExpress (R)-Ketorolac is the R-enantiomer of Ketorolac, shows potent analgesic activity, reduces ulcerogenic potential. (R)-Ketorolac is inactive on COX.
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| Kemisk navn eller materiale | (R)-Ketorolac |
|---|---|
| Sundhedsfare 1 | H315∣H319∣H335 |
| Formel vægt | 255.27 |
| Opløselighedsinformation | DMSO : ≥ 100 mg/mL (391.74 mM) |
| Procent renhed | 98.38% |
| Fysisk form | Solid |
| Farve | Off-White |
| 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) | 255.27 |
| CAS | 66635-93-6 |
| Synonym | (+)-Ketorolac |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(C1=CC=CC=C1)C2=CC=C3N2CC[C@H]3C(O)=O |
| Renhedsgrad noter | Research |
| Molekylær formel | C15H13NO3 |
| Til brug med (applikation) | Neuroscience-Neuromodulation |
YM-90709, MedChemExpress
MedChemExpress YM-90709 is a novel IL-5 inhibitor which selectively blocks the binding of IL-5 to the IL-5 receptor (IL-5R).YM-90709 potently inhibits the binding of [125I]-IL-5 to IL-5R on human peripheral eosinophils and eosinophilic HL-60 clone 15 cells with IC50 values of 1.0 and 0.57 μM.
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| Kemisk navn eller materiale | YM-90709 |
|---|---|
| Formel vægt | 359.42 |
| Opløselighedsinformation | DMSO : 62.5 mg/mL (173.89 mM; Need ultrasonic) |
| Procent renhed | 99.52% |
| Fysisk form | Solid |
| Farve | Orange |
| 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) | 359.42 |
| CAS | 163769-88-8 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | CC(CC1=CC(OC)=C(OC)C=C12)(C)N3C2=CC4=NC5=CC=CC=C5N=C43 |
| Renhedsgrad noter | Research |
| Molekylær formel | C22H21N3O2 |
| Til brug med (applikation) | COVID-19-immunoregulation |
(S)-Ketorolac, MedChemExpress
MedChemExpress (S)-Ketorolac is a nonsteroidal anti-inflammatory agent. (S)-ketorolac exhibits potent COX1 and COX2 enzyme inhibition.
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| Kemisk navn eller materiale | (S)-Ketorolac |
|---|---|
| Formel vægt | 255.27 |
| Opløselighedsinformation | DMSO : 200 mg/mL (783.48 mM; Need ultrasonic) |
| Procent renhed | 99.62% |
| Fysisk form | Solid |
| Farve | Off-White |
| 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) | 255.27 |
| CAS | 66635-92-5 |
| Synonym | (-)-Ketorolac |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(C1=CC=CC=C1)C2=CC=C3N2CC[C@@H]3C(O)=O |
| Renhedsgrad noter | Research |
| Molekylær formel | C15H13NO3 |
| Til brug med (applikation) | Neuroscience-Neuromodulation |
AM679, MedChemExpress
MedChemExpress AM679 is a potent, selective 5-lipoxygenase-activating protein (FLAP) inhibitor with an IC50 of 2 nM in a human FLAP membrane binding assay. AM679 markedly reduces the respiratory syncytial virus-driven ocular pathology as well as the synthesis of cysteinyl leukotrienes (CysLTs) in the eye.
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| Kemisk navn eller materiale | AM679 |
|---|---|
| Formel vægt | 692.87 |
| Opløselighedsinformation | DMSO : ≥ 100 mg/mL (144.33 mM) |
| Procent renhed | 99.6% |
| Fysisk form | Solid |
| Farve | pale pink |
| 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) | 692.87 |
| CAS | 1206880-66-1 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(C)N1C2=CC=CC=C2C[C@H]1COC3=CC=C(N(CC4=CC=C(C5=NC=C(OC)C=N5)C=C4)C(CC(C)(C(O)=O)C)=C6SC(C)(C)C)C6=C3 |
| Renhedsgrad noter | Research |
| Molekylær formel | C40H44N4O5S |
| Til brug med (applikation) | COVID-19-immunoregulation |
GSK376501A, MedChemExpress
MedChemExpress GSK376501A is a selective peroxisome proliferator-activated receptor gamma (PPARγ) modulator for the treatment of type 2 diabetes mellitus.
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VU0661013, MedChemExpress
MedChemExpress VU661013 is a potent and selective MCL-1 inhibitor.
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| Kemisk navn eller materiale | VU0661013 |
|---|---|
| Formel vægt | 712.66 |
| Opløselighedsinformation | DMSO : ≥ 125 mg/mL (175.40 mM) |
| Procent renhed | 98.52% |
| Fysisk form | Solid |
| Farve | Light Yellow |
| Grad | Research |
| Anbefalet opbevaring | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| Molekylvægt (g/mol) | 712.66 |
| CAS | 2131184-57-9 |
| Holdbarhed | Powder -20°C 3 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | ClC1=CC=C(C(CCCOC2=CC(C)=C(Cl)C(C)=C2)=C3N4[C@H](C)CN(C5=CN(C)C6=C5C=C(C(O)=O)C=C6)C3=O)C4=C1C7=C(C)N(C)N=C7C |
| Renhedsgrad noter | Research |
| Molekylær formel | C39H39Cl2N5O4 |
| Til brug med (applikation) | Cancer-programmed cell death |
JNJ-7777120, MedChemExpress
MedChemExpress JNJ-7777120 is a selective H4R antagonist with Ki of 4 ±1 nM, exhibits >1000-fold selectivity over the other histamin receptors.
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| Kemisk navn eller materiale | JNJ-7777120 |
|---|---|
| Sundhedsfare 1 | H315∣H319∣H335 |
| Formel vægt | 277.75 |
| Opløselighedsinformation | DMSO : ≥ 50 mg/mL (180.02 mM) |
| Procent renhed | 98.0% |
| Fysisk form | Solid |
| Farve | White |
| 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) | 277.75 |
| CAS | 459168-41-3 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(C(N1)=CC2=C1C=CC(Cl)=C2)N3CCN(C)CC3 |
| Renhedsgrad noter | Research |
| Molekylær formel | C14H16ClN3O |
| Til brug med (applikation) | COVID-19-immunoregulation |
CAY10650, MedChemExpress
MedChemExpress CAY10650 is a highly potent cytosolic phospholipase A2α (cPLA2α) inhibitor with an IC50 value of 12 nM. CAY10650 suppresses lipid droplets formation and PGE2 secretion.
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| Kemisk navn eller materiale | CAY10650 |
|---|---|
| Formel vægt | 471.5 |
| Opløselighedsinformation | DMSO : ≥ 43 mg/mL (91.20 mM) |
| Procent renhed | 98.0% |
| Fysisk form | Solid |
| Farve | Off-White |
| 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) | 471.5 |
| CAS | 1233706-88-1 |
| Holdbarhed | Powder -20°C 3 years, 4°C 2 years∣In solvent -80°C 6 months, -20°C 1 month |
| SMIL | O=C(CN1C(C=CC(C(O)=O)=C2)=C2C(C(C(C)C)=O)=C1)COC(C=C3)=CC=C3OC4=CC=CC=C4 |
| Renhedsgrad noter | Research |
| Molekylær formel | C28H25NO6 |
| Til brug med (applikation) | COVID-19-immunoregulation |