Carbonyl compounds
Medchemexpress LLC 2'-Fluoro-2'-deoxy-ara-C(Bz)-3'-phosphoramidite | 1404463-12-2 | C46H51FN5O8P | 250 MG
2'-Fluoro-2'-deoxy-ara-C(Bz)-3'-phosphoramidite is a cytidine analog that works by inhibiting DNA methyltransferases. This compound shows potential anti-metabolic and anti-tumor activities.
- Cytidine analog
- Inhibits DNA methyltransferases
- Possesses potential anti-metabolic activities
- Possesses potential anti-tumor activities
- High purity (99.84%)
- Appears as a white to off-white solid
- Stable under recommended storage conditions
- For research use only
Medchemexpress LLC 3'-Azido-3'-deoxy-5-methylcytidine | 1282040-14-5 | 99.9% | 282.26 | 1 ML
3'-Azido-3'-deoxy-5-methylcytidine (CS-92) is a potent xenotropic murine leukemia-related retrovirus (XMRV) inhibitor with a CC50 of 43.5 μM in MCF-7 cells. It also inhibits HIV-1 reverse transcriptase with an EC50 of 0.06 μM in peripheral blood mononuclear (PBM) cells. This compound is a click chemistry reagent, containing an Azide group, and can participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) reactions with molecules containing Alkyne groups. It can also undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- Inhibits HIV-1 at an EC50 of 0.06 μM in PBM cells
- Inhibits XMRV at a CC50 of 43.5 μM in MCF-7 cells
- Functions as a click chemistry reagent
- Contains an Azide group for CuAAc reactions with Alkyne groups
- Participates in SPAAC reactions with DBCO or BCN groups
Medchemexpress LLC 11-Deoxy Prostagland | 1MG
11-Deoxy Prostaglandin E2 is a selective agonist of EP4 with an EC50 of 0 66 nM 11-Deoxy Prostaglandin E2 is an analog of prostaglandin E2 11-Deoxy Prostaglandin E2 can be used in study bone healing heart failure and other receptor associated conditions[1][2]
Medchemexpress LLC 6A-azido-6A-deoxy-β-cyclodextrin | 98169-85-8 | MFCD05864973 | 98.0% | 1,160.00 g·mol⁻¹ | C42H69N3O34 | 10 MG
6A-Azido-6A-deoxy-β-cyclodextrin is a mono-azido functionalized β-cyclodextrin supplied as a solid. It provides an azide handle for copper-catalyzed azide-alkyne cycloaddition (click chemistry) and is used for bioconjugation, drug-delivery research, and surface modification. High purity and defined molecular weight support analytical and synthetic workflows.
- Mono-azido functionality for efficient click chemistry reactions.
- High purity (98.0%) suitable for research applications.
- Water-soluble cyclodextrin derivative for host-guest studies.
- Good solubility in DMSO; ultrasonic assistance recommended.
- Supplied as a solid for convenient handling and storage.
Medchemexpress LLC 5'-Deoxy-5'-iodouridine | 14259-58-6 | 95.0% | C9H11IN2O5 | 1 ML
5'-Deoxy-5'-iodouridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on inhibition of DNA synthesis, induction of apoptosis, etc.
- Purine nucleoside analog
- Broad antitumor activity targeting indolent lymphoid malignancies
- Inhibits DNA synthesis
- Induces apoptosis
Medchemexpress LLC 5'-Deoxy-5'-iodouridine | 14259-58-6 | 95.0% | C9H11IN2O5 | 100 MG
5'-Deoxy-5'-iodouridine is a purine nucleoside analog. Purine nucleoside analogs exhibit broad antitumor activity, specifically targeting indolent lymphoid malignancies. The anticancer mechanisms involved include the inhibition of DNA synthesis and the induction of apoptosis.
- It is a purine nucleoside analog.
- Demonstrates broad antitumor activity.
- Targets indolent lymphoid malignancies.
- Functions by inhibiting DNA synthesis.
- Induces apoptosis.
Medchemexpress LLC Uridine, 3'-deoxy-3'-fluoro- | 57944-13-5 | C9H11FN2O5 | 5 MG
3'-Deoxy-3'-fluorouridine is a purine nucleoside analog with a molecular formula of C9H11FN2O5. It appears as a white to off-white solid and has a high purity of 99.66% as determined by LCMS. This product is intended for research use only and has not been fully validated for medical applications.
- White to off-white solid appearance
- Purity of 99.66% (LCMS)
- Consistent with structure based on 1H NMR spectrum and LCMS
Medchemexpress LLC 2'-Fluoro-2'-deoxy-ara-A(Bz)-3'-phosphoramidite | 329187-86-2 | C47H51FN7O7P | 1 MG
2'-Fluoro-2'-deoxy-ara-A(Bz)-3'-phosphoramidite is an adenosine analog. Adenosine analogs primarily act as smooth muscle vasodilators and have also been shown to inhibit cancer progression.
- Adenosine analog
- Acts as a smooth muscle vasodilator
- Inhibits cancer progression
Medchemexpress LLC 2′-Deoxy-N-methylguanosine | 19916-77-9 | C11H15N5O4 | 100 MG
2'-Deoxy-N2-methylguanosine, a DNA adduct, is classified as a purine nucleoside analog. These analogs demonstrate broad antitumor activity, specifically targeting indolent lymphoid malignancies. The anticancer mechanisms involved include the inhibition of DNA synthesis and the induction of apoptosis.
- Molecular weight: 281.27
- Appearance: Solid
- Color: Off-white to light yellow
- Purity: 99.82%
- Solubility (in vitro): DMSO : 12.5 mg/mL (44.44 mM)
Medchemexpress LLC 2′-Deoxy-N-methylguanosine | 19916-77-9 | C11H15N5O4 | 5 MG
2'-Deoxy-N2-methylguanosine, a DNA adduct, is a purine nucleoside analog. These analogs are known to have broad antitumor activity, particularly against indolent lymphoid malignancies.
- DNA adduct
- Purine nucleoside analog
- Exhibits broad antitumor activity against indolent lymphoid malignancies
- Anticancer mechanisms involve inhibiting DNA synthesis and inducing apoptosis
Medchemexpress LLC 2'-Deoxy-N1-methylguanosine | 5132-79-6 | C₁₁H₁₅N₅O₄ | 50 MG
2'-Deoxy-N1-methylguanosine is a purine nucleoside analog that exhibits broad antitumor activity, specifically targeting indolent lymphoid malignancies. Its anticancer mechanisms include the inhibition of DNA synthesis and the induction of apoptosis.
- Purine nucleoside analog
- Exhibits broad antitumor activity
- Targets indolent lymphoid malignancies
- Inhibits DNA synthesis
- Induces apoptosis