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Filtered Search Results
Medchemexpress LLC Anti-B7-H4 VTCN1 Ant 10mg | 10mg
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Anti-B7-H4/VTCN1 Antibody is a CHO-expressed human antibody that targets B7-H4/VTCN1 The Anti-B7-H4/VTCN1 Antibody contains a huIgG1 heavy chain and a hu light chain with a predicted molecular weight (MW) of 145 kDa The isotype control for Anti-B7-H4/VTCN1 Antibody can be referenced as Human IgG1 kappa Isotype Control (HY-P99001)
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Medchemexpress LLC N-Carbamoyl-DL-aspartic acid | 923-37-5 | 1 G
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N-Carbamoyl-DL-aspartic acid, also known as Ureidosuccinic acid, is a precursor of nucleic acid pyrimidines. It has demonstrated antitumor activities and is considered an endogenous metabolite, playing a role in metabolic enzyme/protease pathways.
- Precursor of nucleic acid pyrimidines
- Exhibits antitumor activities
- Effective in murine Lewis lung carcinoma models
- Reverses toxicity and antitumor activity of N-(phosphonacetyl)-L-aspartate
- Functions as a precursor of nucleic acid pyrimidines in normal and tumor-bearing mice
- Soluble in DMSO for in vitro studies
- Can be formulated for in vivo studies using various solvent systems
- Recommended storage for powder is -20°C for 3 years or 4°C for 2 years
- Recommended storage in solvent is -80°C for 2 years or -20°C for 1 year
- For research use only
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Medchemexpress LLC Hydroxypropyl tetrahydropyrantriol | 439685-79-7 | 98.0% | 192.21 g·mol⁻¹ | C8H16O5 | 250 MG
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Pro-xylane (30% in water) is an aqueous formulation of hydroxypropyl tetrahydropyrantriol used as a cosmetic active to support skin matrix remodeling. It promotes glycosaminoglycan biosynthesis in fibroblasts, enhances dermal collagen and hyaluronic acid production, and is intended for formulation and research use.
- Stimulates glycosaminoglycan synthesis in fibroblasts
- Enhances collagen and hyaluronic acid production in the dermis
- Improves skin hydration and elasticity
- Reduces appearance of wrinkles and supports skin firmness
- Supplied as a 30% aqueous solution with high purity
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Medchemexpress LLC 4-Isopropoxybenzoic acid | 13205-46-4 | 100.0% | C10H12O3 | 250 MG
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4-Isopropoxybenzoic acid is an aromatic carboxylic acid organic compound that can be used as a synthetic intermediate in organic synthesis, such as in pesticides. It is a versatile compound with applications in various chemical processes.
- Aromatic carboxylic acid compound
- Used as a synthetic intermediate in organic synthesis
- Molecular weight: 180.20
- Appearance: Solid
- Color: White to off-white
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eMolecules 1046816-75-4 | (2-CHLOROPYRIMIDIN-5-YL)METHANOL | AstaTech | MFCD16659172 | 144.560 | C5H5ClN2O | 95.000 | OCc1cnc(Cl)nc1 | 5g | 222808806
(2-CHLOROPYRIMIDIN-5-YL)METHANOL | AstaTech | 1046816-75-4 | MFCD16659172 | 144.560 | C5H5ClN2O | 95.000 | OCc1cnc(Cl)nc1 | 5g | 222808806
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Medchemexpress LLC Nh-bis-peg2 | 54384-47-3 | MFCD00239212 | 97.0% | 193.24 g·mol⁻¹ | C8H19NO4 | 250 MG
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NH-bis-PEG2 is a non-cleavable, two-unit polyethylene glycol (PEG) linker used in the synthesis of antibody-drug conjugates (ADCs) and proteolysis targeting chimeras (PROTACs). It provides a short, flexible spacer with a terminal amino (NH) functionality suitable for bioconjugation and linker construction.
- Non-cleavable two-unit PEG linker suitable for ADC and PROTAC synthesis.
- Provides a short, flexible spacer with terminal NH for bioconjugation.
- CAS number 54384-47-3.
- Molecular formula C8H19NO4; molecular weight 193.24 g·mol⁻¹.
- Purity 97.0%.
- Storage: 4°C, protect from light; in solvent: -80°C (6 months), -20°C (1 month).
- Packaged quantity: 250 MG.
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Medchemexpress LLC NOREPINEPHRINE TARTR 250MG | 250MG
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NOREPINEPHRINE TARTR 250MG | 250MG
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Medchemexpress LLC Pepsin | 9001-75-6 | 250 MG
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Pepsin is the major pig and human gastric protease and a minor pepsin-like gastric proteolytic enzyme. It contributes to the proteolysis of food proteins in the vertebrate stomach.
- Optimal pH for activity is 1.0-3.0.
- Activated by hydrochloric acid (HCl) and trifluoroacetic acid (TFA).
- Inactivated by pH greater than 6.0.
- To reconstitute, resuspend in double-distilled water (pH 5.5 or lower) to 1 mg/mL.
- Reconstituted Pepsin can be stored at 4 °C for up to one month.
- Cleavage specificity for Phenylalanine (Phe) and Leucine (Leu) is best at pH 1.0 and decreased above pH 2.0.
- Irreversibly inactivates above pH 6.0.
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![eMolecules 1417789-50-4 | (3aS,6aS)-1-Methyl-hexahydropyrrolo[3,4-b]pyrrole Dihydrochloride | Synthonix199.120 | C7H16Cl2N2 | 95.000 | Cl.Cl.CN1CC[C@H]2CNC[C@@H]12 | 250mg | 722004353](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000126687.jpg-250.jpg)
eMolecules 1417789-50-4 | (3aS,6aS)-1-Methyl-hexahydropyrrolo[3,4-b]pyrrole Dihydrochloride | Synthonix199.120 | C7H16Cl2N2 | 95.000 | Cl.Cl.CN1CC[C@H]2CNC[C@@H]12 | 250mg | 722004353
(3aS,6aS)-1-Methyl-hexahydropyrrolo[3,4-b]pyrrole Dihydrochloride | Synthonix | 1417789-50-4199.120 | C7H16Cl2N2 | 95.000 | Cl.Cl.CN1CC[C@H]2CNC[C@@H]12 | 250mg | 722004353
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eMolecules Ambeed 4-[4-(Hydroxymethyl)benzyl]piperazine N1-BOC protected 250mg 716188382 A252156 0 000 622381-67-3 MFCD06658975 306 406 C17H26N2O3
Ambeed 4-[4-(Hydroxymethyl)benzyl]piperazine N1-BOC protected 250mg 716188382 A252156 0 000 622381-67-3 MFCD06658975 306 406 C17H26N2O3
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Medchemexpress LLC Trisbenzyltriazolylm 250mg | 510758-28-8 | 250 MG
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Tris(benzyltriazolylmethyl)amine (TBTA) is a tridentate ligand used to stabilize copper(I) catalysts in copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions. It is employed to improve efficiency and selectivity in bioconjugation workflows for tagging proteins, peptides, and small molecules.
- Stabilizes Cu(I) to improve click reaction efficiency.
- Enhances yield and selectivity in CuAAC conjugations.
- Suitable for protein, peptide, and small-molecule labeling.
- Available as solid and DMSO solution formats for flexible use.
- High purity supports reproducible experimental results.
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Medchemexpress LLC Acoziborole | 1266084-51-8 | 99.7% | 367.10 | 250 MG
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Acoziborole | 1266084-51-8 | 99.7% | 367.10 | 250 MG
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Medchemexpress LLC UC2288 | 1394011-91-6 | 99.8% | 481.82 | 250 MG
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UC2288 is a potent and orally active p21 attenuator with relatively selective activity for p21. It is synthesized based on Sorafenib and potently inhibits cancer cell growth by inducing apoptosis. UC2288 shows no inhibition of VEGFR2 and Raf kinases even at 10 μM.
- Potent and orally active p21 attenuator
- Induces apoptosis to inhibit cancer cell growth
- Relatively selective activity for p21
- No inhibition of VEGFR2 and Raf kinases at 10 μM
- Decreases p21 protein level and mRNA expression
- Suppresses tumor growth in vivo
- Ameliorates MPTP-induced Parkinson's disease progression
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![Medchemexpress LLC Pyrimido[4,5-d]pyrimidin-2(1H)-one, 7-[[2-methoxy-4-(1-methyl-4-piperidinyl)phenyl]amino]- | 1936529-65-5 | 99.8% | 600.11 | C32H34ClN7O3 | 250 MG](https://assets.fishersci.com/TFS-Assets/CCG/product-images/5000211456.png-250.jpg)
Medchemexpress LLC Pyrimido[4,5-d]pyrimidin-2(1H)-one, 7-[[2-methoxy-4-(1-methyl-4-piperidinyl)phenyl]amino]- | 1936529-65-5 | 99.8% | 600.11 | C32H34ClN7O3 | 250 MG
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YKL-05-099 is a small-molecule salt-inducible kinase (SIK) inhibitor used as a research tool in biochemical and cell-based studies. It exhibits high potency for SIK1 and SIK3, with reported IC50 values in the low nanomolar range, and is applied for kinase assays, signaling investigations, and target validation. The compound has a molecular weight of 600.11 and a reported purity of 99.76%.
- Potent inhibition of SIK1 and SIK3 (IC50 ≈ 10 and 30 nM, respectively).
- Moderate activity against SIK2 (IC50 ≈ 40 nM).
- High chemical purity (99.76%).
- Suitable for biochemical kinase assays and cell-based signaling studies.
- Provided as a solid research compound for laboratory use.
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Medchemexpress LLC TCO-PNB ester | 1438415-89-4 | 98.5% | C15H17NO5 | 25 MG
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TCO-PNB ester is an amine-reactive building block used for the modification of amine-containing molecules. It contains a TCO group that can undergo an inverse electron demand Diels-Alder reaction (iEDDA) with molecules containing a Tetrazine group.
- Amine-reactive building block for modification of amine-containing molecules.
- The TCO group allows for iEDDA reaction with Tetrazine-containing molecules.
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