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Medchemexpress LLC MEDCHEMEXPRESS LLC
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5000431134 PROTOCATECHUALDEHYDE 250G
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eMolecules 36697-72-0 | 4,4',5,5'-Tetrahydro-2,2'-bioxazole | Ambeed | MFCD00059930 | 140.142 | C6H8N2O2 | 97.000 | C1CN=C(O1)C1=NCCO1 | 25g | 572831217
4,4',5,5'-Tetrahydro-2,2'-bioxazole | Ambeed | 36697-72-0 | MFCD00059930 | 140.142 | C6H8N2O2 | 97.000 | C1CN=C(O1)C1=NCCO1 | 25g | 572831217
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eMolecules 3-Fluoro-4-hydroxyphenylacetic acid | 458-09-3 | 1G | Purity: 98%
Matrix Scientific | 3-Fluoro-4-hydroxyphenylacetic acid | 1G | 458-09-3 | MFCD00004348
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eMolecules Building Block Tool
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Medchemexpress LLC Hsp90-in-17 hydrochloride | 1253584-63-2 | 99.31% | 476.87 | 25 MG
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Hsp90-IN-17 hydrochloride is an HSP90 inhibitor that can be used in the study of proliferative diseases, such as cancer and neurodegenerative diseases.
- HSP90 inhibitor
- Used in the study of proliferative diseases
- Suitable for cancer research
- Suitable for neurodegenerative diseases research
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Medchemexpress LLC AS-Patisiran sodium | 1 MG
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AS-Patisiran sodium is an antisense strand of Patisiran. Patisiran is a double-stranded small interfering RNA (siRNA) that targets a sequence within the transthyretin (TTR) messenger RNA. It specifically inhibits hepatic synthesis of mutant and wild-type TTR.
- Targets a sequence within the transthyretin (TTR) messenger RNA
- Specifically inhibits hepatic synthesis of mutant and wild-type TTR
- Can be used for the research of hereditary TTR amyloidosis
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5000586482 CEFTRIAXONE SODIUM 10G
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5000371580 CABOTEGRAVIR SODIUM 10MM 1ML
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Apexbio Technology LLC PTP Inhibitor I 2491-38-5 25g
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PTP Inhibitor I (CAS 2491-38-5) is a small molecule inhibitor targeting protein tyrosine phosphatases (PTPs) specifically SHP-1 and PTP1B with inhibition constants (KI) of 43 M and 42 M respectively As an -bromoacetophenone derivative it acts as a neutral phosphotyrosine mimetic covalently modifying the active site cysteine of PTPs Structure-activity studies indicate that modifications to the phenyl ring moderately affect potency while para-substituted peptidyl groups can enhance both potency and selectivity PTP Inhibitor I is utilized in vitro for mechanistic studies of PTP function related to diabetes neurodegenerative disorders immune regulation and pathogen virulence Animal and clinical data are not available
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5000703838 ANTIVIRAL AGENT 75 1MG
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eMolecules 89402-44-8 | 5-Bromo-2,3-difluoropyridine | Apollo Scientific US - Building Blocks | MFCD06659525 | 193.979 | C5H2BrF2N | 98.000 | Fc1cc(Br)cnc1F | 5g | 489814907
5-Bromo-2,3-difluoropyridine | Apollo Scientific US - Building Blocks | 89402-44-8 | MFCD06659525 | 193.979 | C5H2BrF2N | 98.000 | Fc1cc(Br)cnc1F | 5g | 489814907
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5000703763 FRENLOSIRSEN SODIUM 1MG
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Apexbio Technology LLC Congo Red 573-58-0 10mM (in 1mL DMSO)
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Congo Red (CAS 573-58-0) is a small-molecule inhibitor targeting the vesicular glutamate transporter (VGlut) It is designed to modulate glutamate storage and release thereby influencing synaptic transmission Congo Red exerts its biological activity primarily through selective non-covalent interaction with -sheet-rich structures such as those found in amyloid fibrils Based on these properties Congo Red holds research potential in the detection and qualitative assessment of amyloid deposits in tissue sections characterization of amyloidosis-related samples plant and fungal cell wall amyloids and lipopolysaccharide staining in Gram-negative bacterial outer membranes for biomedical and microbiological studies
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Ambeed AMBEED
5000867409 1-METHYLCYCLOBUTANAMINE HY 5GR
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Medchemexpress LLC Lesinurad sodium | 1151516-14-1 | C17H13BrN3NaO2S | 1 ML
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Lesinurad sodium is a URAT1 and OAT inhibitor, identified as a substrate for kidney transporters OAT1 and OAT3. It is a novel selective uric acid reabsorption inhibitor (SURI) that increases proximal renal tubule urate excretion.
- Acts as a URAT1 and OAT inhibitor
- Functions as a substrate for kidney transporters OAT1 and OAT3
- Increases proximal renal tubule urate excretion
- Inhibits CYP2C9 and CYP2C8
- Suitable for research use only
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Medchemexpress LLC PF-00356231 hydrochloride | 820223-77-6 | 99.0% | 464.96 | 100 MG
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PF-00356231 hydrochloride is a specific, non-peptidic, non-zinc chelating ligand and inhibitor of matrix metalloproteinase MMP-12 (IC50=1.4 μM). It binds to MMP-12, forming a PF-00356231/MMP-12 complex. This compound also demonstrates potency against MMP-13, MMP-8, MMP-9, and MMP-3 with IC50 values of 0.00065, 1.7, 0.98, and 0.39 μM, respectively. It is intended for research use only.
- Specific inhibitor of matrix metalloproteinase MMP-12.
- Non-peptidic and non-zinc chelating ligand.
- Potency against MMP-13, MMP-8, MMP-9, and MMP-3.
- Available in solid and solution forms.
- Can be stored at 4°C (sealed, away from moisture) or -80°C/-20°C in solvent.
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