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Filtered Search Results
Sigma Aldrich Fine Chemicals Biosciences Lonidamine mitochondrial hexokinase inhibitor | 50264-69-2 | MFCD00866285 | 5MG
Lonidamine mitochondrial hexokinase inhibitor | Purity: >=98% (TLC) | Mol Wt: 321.16 | 50264-69-2 | MFCD00866285 | 5MG
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![eMolecules 7672-35-7 | L-Hydroxyprolylglycine | Toronto Research Chemicals | MFCD00037878 | 188.183 | C7H12N2O4O[C@H]1CN[C@@H](C1)C(=O)NCC(O)=O | 100mg | 601596697](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502176150.JPG-250.jpg)
eMolecules 7672-35-7 | L-Hydroxyprolylglycine | Toronto Research Chemicals | MFCD00037878 | 188.183 | C7H12N2O4O[C@H]1CN[C@@H](C1)C(=O)NCC(O)=O | 100mg | 601596697
L-Hydroxyprolylglycine | Toronto Research Chemicals | 7672-35-7 | MFCD00037878 | 188.183 | C7H12N2O4O[C@H]1CN[C@@H](C1)C(=O)NCC(O)=O | 100mg | 601596697
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eMolecules 183293-82-5 | Medchem Express | Gemcabene | 5mg | 475641488 | HY-109567 | MFCD00951832 | 302.411 | C16H30O5
Ambeed | 2-(4-(Ethylsulfinyl)phenyl)-4455-tetramethyl-132-dioxaborolane | 250mg | 718039657 | A1619748 | 2828445-91-4 | 280.190 | C14H21BO3S
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Sigma Aldrich Fine Chemicals Biosciences Stavudine impurity I European Pharmacopoeia (EP) Reference Standard | 122567-97-9 |
Stavudine impurity I European Pharmacopoeia (EP) Reference Standard | Mol Wt: 328.32 | 122567-97-9 |
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Enzo Life Sciences Piceatannol (1mg). CAS: 10083-24-6
Originally isolated from Euphorbia lagascae. Selective protein tyrosine kinase Syk inhibitor (IC50~10 µM). In RBL-2H3 cells the selective inhibition of Syk by piceatannol results in inhibition of FcεR1-mediated signaling. Activator of human deacetylase SIRT1. Alternative name: 3,4,3',5'-Tetrahydroxy-trans-stilbene. Formula: C14H12O4. MW: 244.2. Purity: ≥98% (HPLC (UV)). Appearance: Off-white to light pink crystalline solid. Solubility: Soluble in DMSO (>50mg/ml), methanol (>50mg/ml), dioxan (>50mg/ml), acetonitrile (>50mg/ml); slightly soluble in water (1mg/ml). Long Term Storage: +4°C. Handling: Protect from light and oxygen.
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Medchemexpress LLC Tildipirosin | 328898-40-4 | MFCD13194925 | 10mg
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Tildipirosin | Putity: 99.81% | MW: 734.02 | 328898-40-4 | MFCD13194925 | 10mg
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eMolecules 1173900-33-8 | Medchem Express | AZD 6482 | 5mg | 446258138 | HY-10344 | MFCD16659062 | 408.458 | C22H24N4O4
ChemScene | Phenyl (4-chloro-3-fluorophenyl)carbamate | 100mg | 624161088 | CS-0132885 | 1229603-46-6 | 265.670 | C13H9ClFNO2
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eMolecules Oligomycin B from Streptomyces diastatochromogenes | 11050-94-5 | MFCD00043232 | 10mg
Apollo Scientific | Oligomycin B from Streptomyces diastatochromogenes | 10mg | 562465686 | BIO1004 | | 11050-94-5 | MFCD00043232 | 805.059 | C45H72O12
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Sigma Aldrich Fine Chemicals Biosciences Phleomycin from Streptomyces verticillus powder | 11006-33-0 | MFCD00131846 | 5MG
Phleomycin from Streptomyces verticillus powder | 11006-33-0 | MFCD00131846 | 5MG
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![Medchemexpress LLC 5-[[4-[[(1S)-2-hydroxy-1-phenylethyl]amino]-5-(1,3,4-oxadiazol-2-yl)pyrimidin-2-yl]amino]-3,3-dimeth | 2320462-65-3 | 99.3% | C24H22N6O4 | 10MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000261841.png-250.jpg)
Medchemexpress LLC 5-[[4-[[(1S)-2-hydroxy-1-phenylethyl]amino]-5-(1,3,4-oxadiazol-2-yl)pyrimidin-2-yl]amino]-3,3-dimeth | 2320462-65-3 | 99.3% | C24H22N6O4 | 10MG
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HPK1-IN-7 is a potent, orally active inhibitor of hematopoietic progenitor kinase 1 (HPK1, MAP4K1) with a reported IC50 of 2.6 nM. It is provided as a research-grade small-molecule powder of high purity for use in biochemical and cellular studies of HPK1 signaling pathways.
- Potent HPK1 inhibition with reported IC50 of 2.6 nM.
- High kinome selectivity for reduced off-target activity.
- High purity (99.3%) suitable for research use.
- Molecular formula C24H22N6O4; molecular weight 458.47 g/mol.
- Supplied as a powder for in vitro and in vivo formulation.
- Recommended storage at -20°C for long-term stability.
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eMolecules 896466-04-9 | Medchem Express | AT9283 | 2mg | 446270961 | HY-50514 | MFCD13193062 | 381.44 | C19H23N7O2
Medchem Express | AT9283 | 2mg | 446270961 | HY-50514 | 896466-04-9 | MFCD13193062 | 381.440 | C19H23N7O2
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Apexbio Technology LLC Streptozocin 18883-66-4 200mg
Streptozocin is an antibiotic derivative commonly utilized as an antitumor agent in biomedical research It exerts its biological function primarily through DNA alkylation resulting in targeted cellular toxicity Notably streptozocin selectively acts on pancreatic -cells by depleting intracellular nicotinamide adenine dinucleotide (NAD ) leading to dysregulated glucose metabolism and experimental induction of diabetes mellitus In addition streptozocin is frequently employed in vitro and in vivo to establish diabetic animal models for examination of diabetes-related complications and screening antidiabetic therapies Reported IC50 values vary depending on cell types and conditions with typical values ranging approximately from 11 to 25 M in pancreatic -cell lines
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Medchemexpress LLC HY-100716 50mg Medchemexpress, IPI549 CAS:1693758-51-8 Purity:>98%
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Medchemexpress, HY-100716 50mg IPI549 CAS:1693758-51-8 IPI549 is a potent and selective PI3Kγ inhibitor with an IC50 of 16 nM. IPI549 shows >100-fold selectivity over other lipid and protein kinases. 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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Apexbio Technology LLC Streptomycin sulfate 3810-74-0 10g
Streptomycin sulfate is an aminoglycoside antibiotic targeting the bacterial 30S ribosomal subunit It is designed to inhibit bacterial protein synthesis thereby suppressing bacterial proliferation Streptomycin sulfate exerts its biological activity primarily through inhibition of mRNA translation by binding to the 30S subunit which impairs initiation and elongation processes during protein synthesis and disrupts the ribosome mRNA complex Based on these pharmacological properties streptomycin sulfate holds research potential in microbiological experimentation susceptibility assays bacterial resistance profiling microbial genetics studies and screening of transgenic cells expressing antibiotic-resistance markers
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Medchemexpress LLC HY-112197 5mg Medchemexpress, PKG drug G1 CAS:374703-78-3 Purity:>98%
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Medchemexpress, HY-112197 5mg PKG drug G1 CAS:374703-78-3 PKG drug G1 targets C42 of PKG Iα. PKG drug G1 can couple to vasodilation and blood pressure lowering by a C42 PKG Iα-independent mechanism. 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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