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Filtered Search Results
eMolecules 4-(2-Amino-1,3-thiazol-4-yl)benzoic acid | 216959-94-3 | MFCD01460736 | 1g
Combi-Blocks | 4-(2-Amino-1,3-thiazol-4-yl)benzoic acid | 1g | 448009810 | ST-6032 | 97.000 | 216959-94-3 | MFCD01460736 | 220.250 | C10H8N2O2S
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![eMolecules THIENO[2,3-D]THIAZOL-2-AMINE | 40507-56-0 | MFCD18451327 | 1g](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502198698.JPG-250.jpg)
eMolecules THIENO[2,3-D]THIAZOL-2-AMINE | 40507-56-0 | MFCD18451327 | 1g
AstaTech | THIENO[2,3-D]THIAZOL-2-AMINE | 1g | 587288993 | 93682 | 95.000 | 40507-56-0 | MFCD18451327 | 156.220 | C5H4N2S2
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eMolecules ChemScene / 3-Amino-3-(4-chlorophenyl)cyclobutanol / 100mg / 714105551 / CS-0514394 / 0.000 / 1353636-85-7 / MFCD20524878 / 197.660 / C10H12ClNO
ChemScene / 3-Amino-3-(4-chlorophenyl)cyclobutanol / 100mg / 714105551 / CS-0514394 / 0.000 / 1353636-85-7 / MFCD20524878 / 197.660 / C10H12ClNO
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Medchemexpress LLC (2-Butyl-5-nitrobenzofuran-3-yl)(4-methoxyphenyl)methanone | 141627-42-1 | 99.59% | C20H19NO5 | 10 G
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MedChemExpress HY-75315 is a chemical compound known as (2-Butyl-5-nitrobenzofuran-3-yl)(4-methoxyphenyl)methanone. It serves as a crucial drug intermediate for the synthesis of various active compounds and is intended solely for research purposes.
- Drug intermediate for synthesis of various active compounds
- Intended for research use only
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Medchemexpress LLC 3-fluorobutan-1-amine hydrochloride | 1780799-10-1 | 95.0% | 127.59 g·mol-1 | C4H11ClFN | 1 G
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3-fluorobutan-1-amine hydrochloride is a fluorinated primary amine used as a synthetic intermediate in medicinal chemistry research. It is supplied as an off-white to light yellow solid, with molecular formula C4H11ClFN, molecular weight 127.59 g·mol-1, and typical purity around 95.0%. Storage recommendations: keep sealed at room temperature and protected from moisture and light; in solvent, store at -80°C for long-term preservation.
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BIOHIPPO AAV-TH-taCasp3-TEVp-P2A-EYFP-WPRE-pA
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Recombinant adeno associated virus expressing taCasp3/TEVp fused to EYFP under the TH promoter with WPRE and hGH polyA elements. Offered under the Biohippo AAVX Series with multiple serotypes available including AAV2/1, AAV2/2, AAV2/5, AAV2/6, AAV2/6m, AAV2/6.2FF, AAV2/7m8, AAV2/8, AAV2/9, AAV2/DJ, AAV2/DJ8, AAV2/Retro, AAV2/PHP.eB, AAV2/PHP.B, AAV2/rh10, AAV2/PHP.S, AAV2/anc80, AAV2/B10, AAV2/olig001, AAV2/BI30, AAV2/BR1, AAV2/MG1.2, AAV1/2, AAV2/MaCPNS1, and AAV2/MaCPNS2. Regular titer is greater than or equal to 2.00E+12 vg per mL, with high titer greater than or equal to 1.00E+13 vg per mL available upon request at no additional cost. Customers may specify preferred serotype and titer when placing orders.
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BIOHIPPO AAV-TH-GFP-WPRE-hGH-polyA
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Recombinant adeno associated virus expressing GFP under the TH promoter with WPRE and hGH polyA elements. Offered under the Biohippo AAVX Series with multiple serotypes available including AAV2/1, AAV2/2, AAV2/5, AAV2/6, AAV2/6m, AAV2/6.2FF, AAV2/7m8, AAV2/8, AAV2/9, AAV2/DJ, AAV2/DJ8, AAV2/Retro, AAV2/PHP.eB, AAV2/PHP.B, AAV2/rh10, AAV2/PHP.S, AAV2/anc80, AAV2/B10, AAV2/olig001, AAV2/BI30, AAV2/BR1, AAV2/MG1.2, AAV1/2, AAV2/MaCPNS1, and AAV2/MaCPNS2. Regular titer is greater than or equal to 2.00E+12 vg per mL, with high titer greater than or equal to 1.00E+13 vg per mL available upon request at no additional cost. Customers may specify preferred serotype and titer when placing orders.
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Medchemexpress LLC TH-Z145 | 2260887-57-6 | C16H28O7P2 | 50 MG
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TH-Z145 is a lipophilic bisphosphonate that functions as an FPPS inhibitor with an IC50 of 210 nM. It is intended for research applications only.
- Acts as an FPPS inhibitor
- Exhibits strong prophylactic effects in pathogenic influenza models
- Inhibits tumor growth and prolongs survival in xenograft mice models
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Medchemexpress LLC 2 4-Dimethylthiazole | 1G
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2 4-Dimethylthiazole | 1G
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Medchemexpress LLC (2-Butyl-5-nitrobenzofuran-3-yl)(4-methoxyphenyl)methanone | 141627-42-1 | 99.6% | C20H19NO5 | 25 G
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(2-Butyl-5-nitrobenzofuran-3-yl)(4-methoxyphenyl)methanone is a drug intermediate for the synthesis of various active compounds. It is for research use only.
- Used as a drug intermediate for active compound synthesis
- Molecular weight: 353.37
- Chemical formula: C20H19NO5
- Appearance: Solid, yellow to brown
- Shipping: Room temperature in continental US
- Storage (powder): -20°C for 3 years, 4°C for 2 years
- Storage (in solvent): -80°C for 6 months, -20°C for 1 month
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Medchemexpress LLC (E)-5-fluoro-N-(3-(3-(hydroxyamino)-3-oxoprop-1-en-1-yl)-4-methoxybenzyl)-2-morpholinoben | 3031349-25-1 | 95.0% | 429.44 | 25 MG
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This potent HDAC inhibitor demonstrates IC50s for HDAC1, HDAC2, HDAC3, HDAC6, and HDAC8, and inhibits cell migration and invasion. It induces apoptosis and cell cycle arrest at the G2/M phase, also showing anti-tumor activity.
- Potent inhibition of HDAC1, HDAC2, HDAC3, HDAC6, and HDAC8.
- Inhibits cell migration and invasion, and induces apoptosis and cell cycle arrest at G2/M phase.
- Demonstrates anti-tumor activity.
- Inhibits tubulin polymerization.
- Increases expression of acetylated-α-tubulin and acetyl-histone H3.
- Modulates mitochondrial membrane potential and reactive oxygen species levels.
- Exhibits favorable liver microsomal stability.
- Shows antiproliferative activities in various cancer cell lines.
- Demonstrates antivascular activity and good cardiovascular safety in vivo.
- Reduces tumor weights in allograft mouse models.
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Medchemexpress LLC a-Methyltyrosine methyl ester (hydrochloride) | 7361-31-1 | 98.91% | 245.71 | 25 MG
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α-Methyltyrosine methyl ester hydrochloride is an orally active and competitive tyrosine hydroxylase inhibitor. It inhibits the conversion of tyrosine to dopamine and can be used as a tool for sympathetic nervous system research. In rats, it has been observed to cause kidney damage and urethral calculi.
- Orally active.
- Competitive tyrosine hydroxylase inhibitor.
- Inhibits the conversion of tyrosine to dopamine.
- Can be used as a tool for sympathetic nervous system research.
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Medchemexpress LLC MET kinase-IN-4 | 888719-03-7 | 99.0% | 458.42 | 25 MG
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MET kinase-IN-4 is an orally active Met kinase inhibitor with potent Met kinase inhibitory activity (IC50 value of 1.9 nM). It can be used for cancer research. It also inhibits Flt-3 and VEGFR-2 kinases with IC50 values of 4 nM and 27 nM, respectively. MET kinase-IN-4 (3 μM) shows good metabolic stability in both human and mouse liver microsomes.
- Orally active Met kinase inhibitor.
- Potent Met kinase inhibitory activity with an IC50 value of 1.9 nM.
- Inhibits Flt-3 and VEGFR-2 kinases with IC50 values of 4 nM and 27 nM, respectively.
- Shows good metabolic stability in both human and mouse liver microsomes.
- Possesses a favorable pharmacokinetic profile in mice.
- Demonstrates significant in vivo antitumor activity in the GTL-16 human gastric carcinoma xenograft model.
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Medchemexpress LLC (S)-2-Amino-3,3-diphenylpropanoic acid | 149597-92-2 | 241.29 | 10 G
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(S)-2-Amino-3,3-diphenylpropanoic acid is an alanine derivative commonly used as an ergogenic supplement. It is known to influence the secretion of anabolic hormones, aid in the supply of fuel during exercise, improve mental performance during stress-related tasks, and help prevent exercise-induced muscle damage. This compound is recognized for its beneficial role as a dietary substance.
- Alanine derivative
- Functions as an ergogenic supplement
- Influences anabolic hormone secretion
- Supports fuel supply during exercise
- Enhances mental performance during stress-related tasks
- Helps prevent exercise-induced muscle damage
- Beneficial dietary substance
- Appearance: solid
- Color: white to off-white
- Stable under recommended storage conditions
- Related to peptides and peptide synthesis reagents
- Classified as an amino acid derivative
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Medchemexpress LLC 2-acetylthiazole | 24295-03-2 | MFCD00005324 | 99.5% | 127.16 g/mol | C5H5NOS | 50g
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2-Acetylthiazole (1-(1 3-Thiazol-2-yl)ethanone 1-(Thiazol-2-yl)ethanone Methyl 2-thiazolyl ketone) is a flavor compound 2-Acetylthiazole is a kind of biological materials or organic compounds that are widely used in life science research[1]
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