Piperidines
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Filtered Search Results
Enzo Life Sciences Ceritinib (free base) (50mg). CAS: 1032900-25-6
Ceritinib is a selective inhibitor of ALK, a target found in metastatic non-small cell lung cancer. Purity: ≥99% (HPLC). Solubility: Soluble in DMSO. Long Term Storage: -20°C.
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Sigma Aldrich Fine Chemicals Biosciences Paroxetine hydrochloride hemihydrate >=98% (HPLC), powder | 110429-35-1 | MFCD03658863 | 10MG
Paroxetine hydrochloride hemihydrate >=98% (HPLC), powder | Purity: >=98% (HPLC) | Mol Wt: 374.83 | 110429-35-1 | MFCD03658863 | 10MG
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Medchemexpress LLC BI-9627 hydrochloride | 1422252-46-7 | 98.0% | 392.80 | 50 MG
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BI-9627 hydrochloride is a potent inhibitor of sodium-hydrogen exchanger isoform 1 (NHE1), with IC50 values of 6 nM in intracellular pH recovery (pHi) assays and 31 nM in human platelet swelling assays. It demonstrates over 30-fold selectivity against NHE2 and shows no measurable inhibitory activity against the NHE3 isoform.
- Decreases autophagy in HTR-8/SVneo cells and reduces human sperm pHi.
- Prolongs Ca2+ recovery in hiPSC-CMs; potent in ischemia-reperfusion injury models.
- Low drug-drug interaction (DDI) potential; excellent pharmacokinetics in rat and dog.
- Off-white to light yellow solid appearance.
- Soluble in DMSO (100 mg/mL) and H2O (4.17 mg/mL).
- Solid storage at 4°C; stock solutions at -80°C (6 months) or -20°C (1 month).
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Medchemexpress LLC 4-PHENYLPIPERIDINE 1G
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4-PHENYLPIPERIDINE 1G
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Medchemexpress LLC HY-101040 100mg , Q203 IAP6;Telacebec CAS:1334719-95-7 Purity:98%
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Medchemexpress, HY-101040 100mg Q203 IAP6;Telacebec CAS:1334719-95-7 Formula:C29H28ClF3N4O2 MIC50: 2.7 nM ( Mycobacterium tuberculosis H37Rv) Purity:98% Q203 (IAP6) is a midazopyridine amide compound. Q203 is active against Mycobacterium tuberculosis H37Rv with an MIC 50 of 2.7 nM in culture broth medium. 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.
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Aobchem 1-(3-Bromophenyl)piperidine, AOBCHEM USA 14358-5G. 84964-24-9. MFCD04108532
1-(3-Bromophenyl)piperidine, AOBCHEM USA 14358-5G. 84964-24-9. MFCD04108532
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Medchemexpress LLC 17 0-20 3 PI-D5 500 ug
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17 0-20 3 PI-D5 500UG
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Medchemexpress LLC HY-18332C 5mg Medchemexpress, DOV-216,303 (Free Base) CAS:66504-40-3 Purity:>98%
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Medchemexpress, HY-18332C 5mg DOV-216,303 (Free Base) CAS:66504-40-3 DOV-216,303 (Free Base) is a potent triple serotonin , norepinephrine , and dopamine reuptake inhibitor, with IC 50 values of 14 nM, 20 nM and 78 nM for hSERT, hNET and hDAT, respectively [1] . Has antidepressant-like effects and increases monoamine release in the prefrontal cortex of olfactory bulbectomized (OBX) rats [2] . 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.
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eMolecules 22090-24-0 | 4-Piperidin-1-yl-benzoic acid | Combi-Blocks | MFCD00587602 | 205.257 | C12H15NO2 | 96.000 | OC(=O)c1ccc(cc1)N1CCCCC1 | 1g | 117555318
4-Piperidin-1-yl-benzoic acid | Combi-Blocks | 22090-24-0 | MFCD00587602 | 205.257 | C12H15NO2 | 96.000 | OC(=O)c1ccc(cc1)N1CCCCC1 | 1g | 117555318
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Medchemexpress LLC HY-18071 5mg Medchemexpress, BI-9627 CAS:1204329-34-9 Purity:>98%
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Medchemexpress, HY-18071 5mg BI-9627 CAS:1204329-34-9 BI-9627 is a sodium-hydrogen exchanger isoform 1 (NHE1) inhibitor with an EC 50 of 31 nM [1] . 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.
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Medchemexpress LLC Sinomenine | 115-53-7 | C19H23NO4 | 100 MG
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Sinomenine is an alkaloid extracted from *Sinomenium acutum*. It functions as a blocker of NF-κB activation and also acts as an activator of the μ-opioid receptor.
- Source: extracted from the plant *Sinomenium acutum*.
- NF-κB blocker: inhibits NF-κB activation.
- Μ-Opioid receptor activator: activates the μ-opioid receptor.
- Antiproliferative activity: demonstrated antiproliferative activity against various human cancer cell lines, including K562.
- Anti-inflammatory and analgesic effects: shows anti-inflammatory activity, for instance, by inhibiting LPS-induced nitric oxide production in RAW264.7 cells. In rodents, it produces antinociception in hot plate and tail flick tests and reduces mechanical hypersensitivity in nerve-injured mice.
- Research use: primarily for research purposes.
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Matrix Scientific 4-PHENYLPIPERIDINE MF C11H15N MW 161.25 CAS 771-99-3 MDL MFCD00006002 QTY 5 UOM G
4-PHENYLPIPERIDINE MF C11H15N MW 161.25 CAS 771-99-3 MDL MFCD00006002 QTY 5 UOM G
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Chem-Impex International, Inc. 3-Phenylpiperidine hydrochloride | 3973-62-4 | MFCD02179092 | 1G
3-Phenylpiperidine hydrochloride, 3973-62-4, MFCD02179092, 1G
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Medchemexpress LLC RIDR-PI-103 | 2581114-71-6 | 98.0% | C27H25N7O4 | 25 MG
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RIDR-PI-103 is a reactive oxygen species (ROS)-induced agent release proagent. It features a self-cyclizing moiety linked to a pan-PI3K inhibitor (PI-103). It has been observed that Doxorubicin and RIDR-PI-103 exhibit a synergistic effect in MDA-MB-361 and MDA-MB-231 cells, leading to the inhibition of cancer cell proliferation. This product is intended for research use only.
- Reactive oxygen species (ROS)-induced agent release proagent
- Features a self-cyclizing moiety linked to a pan-PI3K inhibitor (PI-103)
- Exhibits synergistic effect with Doxorubicin in MDA-MB-361 and MDA-MB-231 cells to inhibit cancer cell proliferation
- Targets reactive oxygen species
- Targets immunology/inflammation pathway
- Targets metabolic enzyme/protease pathway
- Targets NF-κB pathway
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eMolecules 677764-87-3 | (4-Piperidin-1-yl-phenyl)methanol | Combi-Blocks | MFCD05864822 | 191.274 | C12H17NO | 98.000 | OCc1ccc(cc1)N1CCCCC1 | 1g | 117555704
(4-Piperidin-1-yl-phenyl)methanol | Combi-Blocks | 677764-87-3 | MFCD05864822 | 191.274 | C12H17NO | 98.000 | OCc1ccc(cc1)N1CCCCC1 | 1g | 117555704
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