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Filtered Search Results
Aobchem (Z)-3 5-difluorobenzaldehyde oxime | ≥97% | CAS 677728-83-5 | C7H5F2NO | 100g
(Z)-3 5-difluorobenzaldehyde oxime | ≥97% | CAS 677728-83-5 | C7H5F2NO | 100g
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Aobchem (Z)-3 5-difluorobenzaldehyde oxime | ≥97% | CAS 677728-83-5 | C7H5F2NO | 5g
(Z)-3 5-difluorobenzaldehyde oxime | ≥97% | CAS 677728-83-5 | C7H5F2NO | 5g
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AA BLOCKS LLC
NC3987582 S-6-METHYLNICOTINE 5G
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Medchemexpress LLC Cis-aconitic acid | 585-84-2 | MFCD00063184 | 99.3% | 174.11 g/mol | C6H6O6 | 5 MG
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(Z)-Aconitic acid is a tricarboxylic organic acid used as a research reagent in biochemical and pharmacological studies. It has reported activity as a glutamate decarboxylase inhibitor, reduces IκB-α phosphorylation, and has been used in models of antigen-induced arthritis and monosodium urate-induced gout. Available in solid form and as DMSO solutions for in vitro and in vivo applications.
- High purity suitable for research applications.
- Available in small solid quantities and DMSO solutions.
- Used in biochemical assays and pharmacological studies.
- Reported to inhibit glutamate decarboxylase activity.
- Documented activity in inflammatory disease models.
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Medchemexpress LLC Cbz-leucinyl-leucinyl-norleucinal | 133407-83-7 | 97.6% | 10 MG
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Z-LLNle-CHO (Cbz-leucinyl-leucinyl-norleucinal) is a peptidic aldehyde inhibitor of γ-secretase used in biochemical and cell-based research. It is supplied as a high-purity solid suitable for in vitro assays.
- Peptidic aldehyde inhibitor of γ-secretase.
- High purity suitable for biochemical and cell-based assays.
- Molecular weight 475.62 g/mol and formula C26H41N3O5.
- Supplied as a small, easily weighed solid for laboratory use.
- Used to study apoptosis, proteasome, and protease pathways.
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Ambeed AMBEED
5000887639 Z-11-TETRADECEN-1-YLACET 100MG
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Medchemexpress LLC (Z)-Guggulsterone | 39025-23-5 | 99.4% | 312.45 | 10 MG
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(Z)-Guggulsterone is a constituent of the Indian Ayurvedic medicinal plant *Commiphora mukul*. It inhibits the growth of human prostate cancer cells by causing apoptosis and inhibits angiogenesis by suppressing the VEGF-VEGF-R2-Akt signaling axis. It also acts as a potent FXR antagonist and reduces ACE2 expression and SARS-CoV-2 infection.
- Inhibits growth of human prostate cancer cells by causing apoptosis
- Inhibits angiogenesis by suppressing the VEGF-VEGF-R2-Akt signaling axis
- Acts as a potent FXR antagonist
- Reduces ACE2 expression
- Reduces SARS-CoV-2 infection
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Aobchem (Z)-2 3 6-trifluorobenzaldehyde oxime | 95% | CAS 1353013-21-4 | C7H4F3NO | 250mg
(Z)-2 3 6-trifluorobenzaldehyde oxime | 95% | CAS 1353013-21-4 | C7H4F3NO | 250mg
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Aobchem (Z)-2 3 6-trifluorobenzaldehyde oxime | 95% | CAS 1353013-21-4 | C7H4F3NO | 500mg
(Z)-2 3 6-trifluorobenzaldehyde oxime | 95% | CAS 1353013-21-4 | C7H4F3NO | 500mg
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AARON CHEMICALS LLC
NC3909337 3-3 4IMETHOXYPHENYLPROPION
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Medchemexpress LLC E/Z-HA155 25mg | 1229652-22-5 | 463.29 | C24H19BFNO5S | 25 MG
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A potent autotaxin (ATX) type I inhibitor for laboratory research, (E/Z)-HA155 is used to study cancer, fibrotic disease, inflammation, pain, and angiogenesis. The product is supplied as a high-purity solid and includes supporting structural and stability data for experimental use.
- Potent autotaxin (ATX) type I inhibitor for mechanistic and pharmacology studies.
- High purity suitable for analytical and biological assays.
- Supplied as a solid 25 mg quantity for small-scale experiments.
- Stable when stored as a powder at -20°C for extended periods.
- Structural identifiers and formula provided for computational and analytical workflows.
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Medchemexpress LLC Z-3578 | 5MG
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Z-3578 | 5MG
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Ambeed AMBEED
5000895570 1-CBZ-AMINO-2-METHYLAMIN 250MG
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Apexbio Technology LLC Z-FA-FMK 105637-38-5;197855-65-5 10mg
Z-FA-FMK is a peptidyl fluoromethyl ketone inhibitor targeting cysteine proteases specifically cathepsins such as cathepsin B and certain caspases It does not require a P1 aspartate residue for inhibition Mechanistically Z-FA-FMK suppresses the enzyme activity of effector caspases (including caspases-2 -3 -6 and -7) but shows minimal impact on initiator caspases (caspase-8 and caspase-10) and only partial attenuation of caspase-9 activity As a negative control inhibitor Z-FA-FMK is regularly applied in apoptosis research to differentiate specific caspase-dependent signaling pathways and to assess the role of cathepsins and caspases in biological contexts such as cell death mechanisms and related pathways
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STA Pharmaceutical DNA C(Bz) amidite | 1 g | CAS 102212-98-6 | MDL MFCD00036315
DNA C(Bz) amidite is a Amidite reagent (Subcategory: Cytosine Series) sold by WuXi TIDES. Offered in 1 g. Store at -20 °C. SDS available for reference.
Specifications
- CAS: 102212-98-6
- MDL: MFCD00036315
- InChIKey: PGTNFMKLGRFZDX-SALLYJDFSA-N
- Molecular Weight: 833.922761998
- Molecular Formula: C46H52N5O8P
- Purity: ≥99%
- Container Type: 30 mL Glass (28-400)
- Pack Size: 1 g
- Net Weight: 1 g
- Gross Weight: 50.1 g
- Commodity Code: 29349990
- Country Of Origin: China
- IUPAC: (2R,3S,5R)-5-(4-benzamido-2-oxopyrimidin-1(2H)-yl)-2-((bis(4-methoxyphenyl)(phenyl)methoxy)methyl)tetrahydrofuran-3-yl (2-cyanoethyl) diisopropylphosphoramidite
- SMILES: CC(N(P(O[C@H]1C[C@H](N2C(N=C(C=C2)NC(C3=CC=CC=C3)=O)=O)O[C@@H]1COC(C4=CC=C(C=C4)OC)(C5=CC=C(C=C5)OC)C6=CC=CC=C6)OCCC#N)C(C)C)C
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