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Filtered Search Results
eMolecules 5273-86-9 | Medchem Express | Beta-asarone | 5mg | 533802727 | HY-N1501 | MFCD00009281 | 208.257 | C12H16O3
Medchem Express | Beta-asarone | 5mg | 533802727 | HY-N1501 | 5273-86-9 | MFCD00009281 | 208.257 | C12H16O3
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Medchemexpress LLC (R)-3-(2-chlorophenyl)-N-(1-(3-methoxyphenyl)ethyl)propan-1-amine hydrochloride | 177172-49-5 | MFCD16038895 | 99.7% | 340.3 g/mol | C18H23Cl2NO | 50 MG
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Tecalcet hydrochloride is the hydrochloride salt of a calcimimetic research compound that allosterically and positively modulates the calcium-sensing receptor (CaSR), increasing receptor sensitivity to extracellular calcium. It is provided for research use in solid form or as DMSO solutions for in vitro studies of CaSR signaling and calcium homeostasis.
- Allosteric positive modulator of the calcium-sensing receptor for CaSR signaling studies.
- Orally active compound used in pharmacology and cellular assays.
- High reported purity suitable for research applications.
- Available as solid and as DMSO solutions for flexible dosing.
- Stable when stored sealed and protected from moisture; solvent storage at low temperatures recommended.
- Well characterized chemically with reported molecular weight and structural identifiers.
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eMolecules 357-70-0 | Medchem Express | Galanthamine | 50mg | 446271480 | HY-76299 | MFCD00867189 | 287.359 | C17H21NO3
Ambeed | 5-Methyl-2-(4455-tetramethyl-132-dioxaborolan-2-yl)aniline | 100mg | 704973383 | A767206 | 863578-36-3 | MFCD06795679 | 233.120 | C13H20BNO2
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Medchemexpress LLC HY-15996A 5mg Medchemexpress, Seviteronel (R enantiomer) CAS:1375603-38-5 Purity:>98%
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Medchemexpress, HY-15996A 5mg Seviteronel (R enantiomer) CAS:1375603-38-5 Seviteronel R enantiomer (VT-464 R enantiomer) is the R enantiomer of Seviteronel (VT-464), which is a potent CYP17 lyase inhibitor(h-Lyase IC50=69 nM); Seviteronel (VT-464) R enantiomer's activity is unknown. 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 Azemiglitazone potas 50mg | 1314533-27-1 | 50MG
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Azemiglitazone potassium (MSDC-0602K) a PPAR -sparing thiazolidinedione (Ps-TZD) binds to PPAR with the IC50 of 18 25 M[1 Azemiglitazone potassium modulates the mitochondrial pyruvate carrier (MPC) Azemiglitazone potassium can be used for the research of fatty liver including dysfunctional lipid metabolism inflammation and insulin resistance[2 Azemiglitazone potassium an insulin sensitizer improves insulinemia and fatty liver disease in mice alone and in combination with Liraglutide[3
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Aobchem AOBCHEM
5000926086 4-PHENOXY-2-METHOXYPHENYLBORON
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Aobchem AOBCHEM
5000926857 1-CHLORO-4-PHENOXY-2- TRIFLUOR
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Aobchem AOBCHEM
5000927239 4- 4- METHYLTHIO PHENOXY TETRA
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Aobchem AOBCHEM
5000936083 1- 4- 4- TERT-BUTYL PHENOXY M
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Medchemexpress LLC HY-101766 5mg Medchemexpress, Btk inhibitor 2 CAS:1558036-85-3 Purity:>98%
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Medchemexpress, HY-101766 5mg Btk inhibitor 2 CAS:1558036-85-3 Btk inhibitor 2 (BGB-3111 analog) is a Bruton's tyrosine kinase ( BTK ) inhibitor extracted from patent US 20170224688 A1. 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 HY-19694 5mg Medchemexpress, BRD7552 CAS:1137359-47-7 Purity:>98%
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Medchemexpress, HY-19694 5mg BRD7552 CAS:1137359-47-7 BRD7552, a potent PDX1 transcription factor inducer, upregulates PDX1 expression in both primary human islets and ductal cells, and induces epigenetic changes in the PDX1 promoter consistent with transcriptional activation. BRD7552 increases insulin expression. PDX1 is a key transcription factor involved in pancreas development and β cell function. 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 HY-114286A 5mg Medchemexpress, PXS-5153A (monohydrochloride) CAS: Purity:>98%
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Medchemexpress, HY-114286A 5mg PXS-5153A (monoHCl) CAS: PXS-5153A monohydrochloride is a potent, selective, orally active and fast-acting lysyl oxidase like 2/3 enzymatic (LOXL2/LOXL3) inhibitor, with an IC50 of <40 nM for LOXL2 across all mammalian species and an IC50 of 63 nM for human LOXL3. PXS-5153A monohydrochloride could reduce crosslinks and ameliorates fibrosis. 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 HY-100729 5mg Medchemexpress, GSK9311 CAS:1923851-49-3 Purity:>98%
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Medchemexpress, HY-100729 5mg GSK9311 CAS:1923851-49-3 GSK9311 is a potent inhibitor of the BRPF bromodomain with pIC 50 values of 6.0 and 4.3 for BRPF1 and BRPF2, respectively. 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 HY-103083 5mg Medchemexpress, GPR40 agonist 4 CAS:2102196-57-4 Purity:>98%
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Medchemexpress, HY-103083 5mg GPR40 agonist 4 CAS:2102196-57-4 GPR40 agonist 4 is a potent free fatty acid receptor 1 (FFA1/ GPR40) agonist with a pEC50 of 7.54. 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 Nvp-tnks656 | 1419949-20-4 | MFCD28167762 | >98.0% | 494.58 g/mol | C27H34N4O5 | 5 MG
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NVP-TNKS656 is a potent, selective, and orally active inhibitor of tankyrase 2 (TNKS2) with a reported IC50 of 6 nM and >300-fold selectivity versus PARP1 and PARP2. It is used as a research tool to study TNKS-mediated regulation of Wnt signaling and related cellular pathways, and is supplied in small research-scale quantities suitable for biochemical and cell-based assays.
- Potent TNKS2 inhibition (IC50 ≈ 6 nM).
- High selectivity versus PARP1 and PARP2 (>300-fold).
- Orally active profile for in vivo study applications.
- Appropriate for biochemical and cell-based assays.
- Available in small-mass formats for research use.
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