Piperidines
Enzo Life Sciences dBET1 (25mg). CAS: 1799711-21-9
dBET1 is a PROTAC, consisting of a BRD4-ligand JQ-1 linked to a cereblon E3 ligase ligand, targeting on BET bromodomain BRD4. Purity: ≥99%. Long Term Storage: -20°C.
Medchemexpress LLC HY-111556 10mg Medchemexpress, BSJ-03-123 CAS: Purity:>98%
Medchemexpress, HY-111556 10mg BSJ-03-123 CAS: BSJ-03-123 is a potent and novel CDK6-selective small-molecule degrader (PROTAC). Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-105545 50mg Medchemexpress, Dexetimide CAS:21888-98-2 Purity:>98%
Medchemexpress, HY-105545 50mg Dexetimide CAS:21888-98-2 Dexetimide ((+)-Benzetimide) is a high-affinity muscarinic receptor antagonist and a potent and persistent anticholinergic agent used to treat neuroleptic-induced parkinsonism. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC HY-10619 50mg Medchemexpress, Niraparib CAS:1038915-60-4 Purity:>98%
Medchemexpress, HY-10619 50mg Niraparib CAS:1038915-60-4 Niraparib (MK-4827) is a highly potent and orally bioavailable PARP1 and PARP2 inhibitor with IC50s of 3.8 and 2.1 nM, respectively. Niraparib leads to inhibition of repair of DNA damage, activates apoptosis and shows anti-tumor activity[2][3]. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
Medchemexpress LLC SERCA2a activator 1 (compound A) | 2139330-34-8 | 99.7% | 551.66 g/mol | C32H29N3O4S | 50MG
SERCA2a activator 1 is a small-molecule activator of the sarco/endoplasmic reticulum Ca2+-dependent ATPase 2a (SERCA2a). It reduces phospholamban-mediated inhibition and can enhance cardiac contractile and relaxation responses in preclinical models. The compound is supplied for research use as a high-purity solid and is also available as a DMSO solution for assay use.
- Activates SERCA2a to improve calcium handling in cardiac models.
- High purity: 99.7%.
- Molecular weight: 551.66 g/mol.
- Chemical formula: C32H29N3O4S.
- Physical form: light yellow to yellow solid powder.
- Available as powder and as a 10 mM solution in DMSO.
- Storage: powder -20°C (up to 3 years) or 4°C (up to 2 years); in solvent -80°C (up to 6 months).
eMolecules 1936529-65-5 | Medchem Express | YKL-05-099 | 5mg | 446256520 | HY-101147 | MFCD31382123 | 600.12 | C32H34ClN7O3
Ambeed | 2-(Cyclopropanecarboxamido)-4567-tetrahydrobenzo[b]thiophene-3-carboxamide | 5mg | 534568377 | A499106 | 329221-38-7 | MFCD00785286 | 264.340 | C13H16N2O2S
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eMolecules 1204329-34-9 | Medchem Express | BI-9627 | 5mg | 455326299 | HY-18071 | MFCD25976925 | 356.349 | C16H19F3N4O2
Ambeed | 4-Bromo-2-fluoro-3-methylpyridine | 100mg | 521423755 | A215661 | 128071-79-4 | MFCD09839278 | 190.015 | C6H5BrFN
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Medchemexpress LLC Pi-Methylimidazoleacetic acid hydrochloride | 1071661-55-6 | 99.01% | 176.60 | 1 ML
Pi-Methylimidazoleacetic acid hydrochloride is a potential neurotoxin and an endogenous metabolite. It is for research use only and not sold to patients.
- Endogenous metabolite
- Potential neurotoxin
Medchemexpress LLC 1-(Chlorocarbonyl)piperidine-d10 | 1219803-31-2 | 98.2% | 157.66 | 1 MG
1-(Chlorocarbonyl)piperidine-d10 is the deuterium labeled 1-(Chlorocarbonyl)piperidine. Deuteration has the potential to affect the pharmacokinetic and metabolic profiles of drugs.
- Can be used as a tracer.
- Can be used as an internal standard for quantitative analysis by NMR, GC-MS, or LC-MS.
![Medchemexpress LLC 5'-benzyl-1'-butyl-N-(naphthalen-2-ylsulfonyl)-6'-oxo-1',6'-dihydro-[2,3'-bipyridine]-4-carboxamide | 2139330-34-8 | 99.5% | 551.66 g·mol⁻¹ | C32H29N3O4S | 5MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000235385.png-250.jpg)
Medchemexpress LLC 5'-benzyl-1'-butyl-N-(naphthalen-2-ylsulfonyl)-6'-oxo-1',6'-dihydro-[2,3'-bipyridine]-4-carboxamide | 2139330-34-8 | 99.5% | 551.66 g·mol⁻¹ | C32H29N3O4S | 5MG
SERCA2a activator 1 is a small-molecule activator of the sarco/endoplasmic reticulum Ca2+-dependent ATPase 2a (SERCA2a) used in preclinical cardiovascular research to attenuate phospholamban inhibition and enhance cardiac contractile function. Supplied for research use only.
- Activates SERCA2a and attenuates phospholamban inhibition.
- Used to enhance systolic and diastolic cardiac function in research models.
- Molecular formula C32H29N3O4S.
- Molecular weight 551.66 g·mol⁻¹.
- Available in milligram quantities suitable for in vitro and in vivo studies.
- Supplied for research use only; not for human or veterinary use.
![Medchemexpress LLC 2-[(2-phenylethyl)thio]nicotinic acid | 496775-95-2 | MFCD03621206 | 99.8% | 259.32 g/mol | C14H13NO2S | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000237749.png-250.jpg)
Medchemexpress LLC 2-[(2-phenylethyl)thio]nicotinic acid | 496775-95-2 | MFCD03621206 | 99.8% | 259.32 g/mol | C14H13NO2S | 10MG
ML-099 (2-[(2-phenylethyl)thio]nicotinic acid) is a small-molecule pan Ras-family GTPase activator used in biochemical and cell-based research to activate Rac1, CDC42, Ras, Rab7, and Rab-2A. It is supplied for research use and is characterized by high purity and a molecular weight of 259.32 g/mol.
- Activates multiple Ras-family GTPases including Rac1 and CDC42.
- Useful for cell-based and biochemical assays probing GTPase signaling.
- High purity for research applications (reported 99.75%).
- Molecular formula C14H13NO2S and molecular weight 259.32 g/mol.
- Identified by CAS 496775-95-2 and PubChem CID 888706.
Medchemexpress LLC PI-103 | 371935-74-9 | 99.8% | 348.36 | 25 MG
PI-103 is a potent PI3K and mTOR inhibitor that also inhibits DNA-PK and induces autophagy. It shows antiproliferative effects in human cancer cell lines, leading to cell cycle arrest, inhibition of leukemic proliferation, and mitochondrial apoptosis. In vivo, it demonstrates therapeutic activity against human tumor xenografts, inhibiting angiogenesis, invasion, and metastasis.
- Potent PI3K and mTOR inhibitor
- Inhibits DNA-PK
- Induces autophagy
- Demonstrates antiproliferative properties in human cancer cell lines
- Induces cell cycle arrest in G1 phase
- Inhibits leukemic proliferation and mitochondrial apoptosis
- Exhibits therapeutic activity against human tumor xenografts
- Inhibits angiogenesis, invasion, and metastasis
- Provides direct antiproliferative effects
Medchemexpress LLC HY-10619D 5mg Medchemexpress, Niraparib R-enantiomer CAS:1038915-58-0 Purity:>98%
Medchemexpress, HY-10619D 5mg Niraparib R-enantiomer CAS:1038915-58-0 Niraparib R-enantiomer (MK-4827 R-enantiomer) is an excellent PARP1 inhibitor with IC50 of 2.4 nM. Purity:>98% Medchemexpress has over 10000 novel life-science reagents, reference compounds, APIs and natural compounds for laboratory and scientific use. Other quantity can also be offered.
eMolecules 3466-80-6 | Ambeed | 2-Phenylpiperidine | 1g | 491166965 | A118058 | MFCD00270125 | 161.248 | C11H15N
ChemScene | 4-(2-Bromophenyl)oxazole | 100mg | 712833151 | CS-0366275 | 850349-06-3 | MFCD08706070 | 224.057 | C9H6BrNO
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