Nucleosides
Chem-Impex International, Inc. 2'-Deoxy-L-thymidine | MFCD02683612 | 1G
2'-Deoxy-L-thymidine, MFCD02683612, 1G
![eMolecules Broadpharm / 5-O-DMT-N2-Isobutyryl-Guanosine / 5g / 761707755 / BP-58850 / / 81246-83-5 / [null] / 655.708 / C35H37N5O8](https://assets.fishersci.com/TFS-Assets/CCG/product-images/502461901.JPG-250.jpg)
eMolecules Broadpharm / 5-O-DMT-N2-Isobutyryl-Guanosine / 5g / 761707755 / BP-58850 / / 81246-83-5 / [null] / 655.708 / C35H37N5O8
Broadpharm / 5-O-DMT-N2-Isobutyryl-Guanosine / 5g / 761707755 / BP-58850 / / 81246-83-5 / [null] / 655.708 / C35H37N5O8
Medchemexpress LLC Trifluridine (Trifluorothymidine) | 70-00-8 | 99.98% | C10H11F3N2O5 | 100 MG
Trifluridine is an irreversible and orally active thymidylate synthase inhibitor that suppresses DNA synthesis. It is an antiviral molecule and an anticancer agent, used in research for various infections and tumors.
Cayman Chemical thIo-p-ToluamIde 5g
A cyclic thioamide building block used in drug discovery chemistry
Selleck Chemical LLC Trifluridine (NSC 75520) S1778-50mg
Trifluridine (NSC 529182 NSC 75520 Viroptic Trifluorothymidine TFT) is an anti-herpesvirus antiviral agent by interacting viral DNA replication used primarily on the eye
Medchemexpress LLC Nucleoside-Analog-1 | 876707-99-2 | 95.0% | C9H9N5O5 | 100 MG
Nucleoside-Analog-1 is a click chemistry reagent containing an azide group. It can participate in copper-catalyzed azide-alkyne cycloaddition reactions (CuAAc) with molecules that have alkyne groups. Additionally, it can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with molecules containing DBCO or BCN groups.
- Click chemistry reagent with an azide group
- Participates in copper-catalyzed azide-alkyne cycloaddition reactions
- Undergoes strain-promoted alkyne-azide cycloaddition reactions
- Purity of 95.0%
- Molecular formula C9H9N5O5
- Appearance: White to off-white solid
- Related to anti-infection and cell cycle/DNA damage pathways
- Associated with disease areas like cancer, infection, and hepatitis C virus infection
Medchemexpress LLC Pseudouridine | 1445-07-4 | 99.9% | 244.20 | 10 MG
Pseudouridine is an isomer of uridine and the most abundant modified nucleoside found in non-coding RNA. It plays a crucial role in fine-tuning and stabilizing regional structures in rRNA and tRNA, which are essential for their functions in mRNA decoding, ribosome assembly, processing, and translation. Pseudouridine-modified tRNA fragments show potential for inhibiting aberrant protein synthesis and are promising for research related to myelodysplastic syndrome (MDS)-related leukemia.
- Isomer of uridine and most abundant modified nucleoside in non-coding RNA.
- Fine-tunes and stabilizes regional structures in rRNA and tRNA.
- Essential for mRNA decoding, ribosome assembly, processing, and translation.
- Pseudouridine-modified tRNA fragments can inhibit aberrant protein synthesis.
- Holds promise for research on myelodysplastic syndrome (MDS)-related leukemia.
Sigma Aldrich Fine Chemicals Biosciences Abacavir Related Compound A United States Pharmacopeia (USP) Reference Standard | 124752-25-6 | 20MG
Abacavir Related Compound A United States Pharmacopeia (USP) Reference Standard | Mol Wt: 246.27 | 124752-25-6 | 20MG
Sigma Aldrich Fine Chemicals Biosciences Guanosine 5′-(B-thio)diphosphate trilithium salt | 97952-36-8 | MFCD00057735 | 5mg
Guanosine 5′-(B-thio)diphosphate trilithium salt | Purity: ≥85% | Mol Wt: 477.07 | 97952-36-8 | MFCD00057735 | 5mg
Medchemexpress LLC 5-Methylcytidine | 2140-61-6 | 99.9% | 257.24 | 100 MG
5-Methylcytidine is a nucleoside compound with antiviral activity, showing an IC50 against HSV-1 of 0.06 μM. It is formed by the attachment of a methyl group to the 5th carbon atom of cytosine. This compound is a common modification in DNA, playing a crucial role in gene expression regulation and development, and is associated with the occurrence and development of diseases such as cancer. It is intended for research use only.
- Has antiviral activity against HSV-1
- Plays a crucial role in gene expression regulation and development
- Associated with the occurrence and development of diseases such as cancer
- For research use only
Selleck Chemical LLC 2-Deoxyadenosine 5-monophosphate S3248-5mg
2 -Deoxyadenosine 5 -monophosphate (5 -dAMP) an endogenous metabolite is only photosensitized degraded under acidic conditions
Medchemexpress LLC Nucleoside-Analog-2 | 876708-01-9 | ≥95.0% | C9H11N5O6 | 100 MG
Nucleoside-Analog-2 is a 4'-Azidocytidine analogue primarily designed to act against Hepatitis C virus (HCV) replication. It functions as a versatile click chemistry reagent, featuring an Azide group, which enables participation in both copper-catalyzed azide-alkyne cycloaddition (CuAAc) and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions.
- Acts against hepatitis C virus (HCV) replication
- Functions as a click chemistry reagent
- Contains an azide group for CuAAc reactions with alkyne-containing molecules
- Undergoes SPAAC reactions with DBCO or BCN group-containing molecules
- Intended for research use only
Medchemexpress LLC HY-N0097 1g Medchemexpress, Guanosine CAS:118-00-3 Purity:>98%
Medchemexpress, HY-N0097 1g Guanosine CAS:118-00-3 Guanosine is a purine nucleoside comprising guanine attached to a ribose (ribofuranose) ring via a β-N9-glycosidic bond. 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.
Medchemexpress LLC Nucleoside-Analog-2 | 876708-01-9 | ≥95.0% | C9H11N5O6 | 1 ML
Nucleoside-Analog-2 is a 4'-Azidocytidine analogue effective against Hepatitis C virus (HCV) replication. It functions as a click chemistry reagent containing an Azide group, enabling it to participate in copper-catalyzed azide-alkyne cycloaddition (CuAAc) with Alkyne groups and strain-promoted alkyne-azide cycloaddition (SPAAC) reactions with DBCO or BCN groups. This product is intended for research use only.
- 4'-Azidocytidine analogue
- Active against Hepatitis C virus (HCV) replication
- Click chemistry reagent
- Contains an Azide group
- Can undergo copper-catalyzed azide-alkyne cycloaddition reaction (CuAAc)
- Can undergo strain-promoted alkyne-azide cycloaddition (SPAAC) reactions