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MEDCHEMEXPRESS LLC MEROPENEM TRIHYDRATE 50MG
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501872934 MEROPENEM TRIHYDRATE 50MG
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MEDCHEMEXPRESS LLC MILTEFOSINE 100MG
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MEDCHEMEXPRESS LLC EGLUMEGAD 5MG
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501873704 EGLUMEGAD 5MG
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MEDCHEMEXPRESS LLC TRANS-ZEATIN 10MG
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501873755 TRANS-ZEATIN 10MG
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MEDCHEMEXPRESS LLC FOSFRUCTOSE TRISODIUM 100MG
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501872151 FOSFRUCTOSE TRISODIUM 100MG
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MEDCHEMEXPRESS LLC LEQ506 5MG
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501873664 LEQ506 5MG
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eMolecules 81189-92-6 | Medchem Express | Acetyllovastatin | 5mg | 482204294 | HY-126237 | 446.584 | C26H38O6
Medchem Express | Acetyllovastatin | 5mg | 482204294 | HY-126237 | 81189-92-6 | 446.584 | C26H38O6
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MEDCHEMEXPRESS LLC GESTRINONE 5MG
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501871823 GESTRINONE 5MG
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MEDCHEMEXPRESS LLC ALLOPURINOL RIBOSIDE 5MG
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501871819 ALLOPURINOL RIBOSIDE 5MG
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Medchemexpress LLC Carbetocin (acetate) | 1631754-28-3 | 99.6% | 1048.21 | 5 MG
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Carbetocin acetate is an oxytocin (OT) analogue and an oxytocin receptor agonist with a Ki of 7.1 nM. It shows high affinity to the chimeric N-terminus (E1) of the oxytocin receptor (Ki=1.17 μM). This compound has potential for research related to postpartum hemorrhage and can cross the blood-brain barrier, exhibiting antidepressant-like activity through the activation of oxytocin receptors in the central nervous system.
- Oxytocin (OT) analogue and oxytocin receptor agonist.
- Ki of 7.1 nM for oxytocin receptor.
- High affinity to chimeric N-terminus (E1) of the oxytocin receptor (Ki=1.17 μM).
- Potential for postpartum hemorrhage research.
- Can cross the blood-brain barrier.
- Produces antidepressant-like activity via activation of oxytocin receptors in the CNS.
- Agonist with significantly higher stability and longer duration of action compared to oxytocin.
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MEDCHEMEXPRESS LLC NEDAPLATIN 10MG
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501872940 NEDAPLATIN 10MG
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MEDCHEMEXPRESS LLC RG108 10MG
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501872926 RG108 10MG
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eMolecules 1628210-26-3 | Medchem Express | KDM5-IN-1 | 1mg | 446255438 | HY-100422 | MFCD30747843 | 324.388 | C17H20N6O
Medchem Express | Bractoppin | 5mg | 586608695 | HY-126020 | 2290527-07-8 | 414.484 | C25H23FN4O
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Medchemexpress LLC Selisistat | 49843-98-3 | C13H13ClN2O | 5 MG
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Selisistat (EX-527) is a potent and selective SirT1 (Sir2 in *Drosophila melanogaster*) inhibitor with an IC50 of 123 nM for SirT1. This compound has been shown to alleviate pathology in various animal and cell models of Huntington's disease.
- Potent and selective SirT1 inhibitor
- Alleviates pathology in multiple animal and cell models of Huntington's disease
- Inhibits the deacetylation activity of human SirT1 and Drosophila Sir2 in transfected cells
- Protective in the R6/2 mouse model of Huntington's disease
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MEDCHEMEXPRESS LLC PF-04447943 5MG
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501873230 PF-04447943 5MG
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