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Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!2025-02-06
19 Results for "
Human Adenovirus
" in MedChemExpress (MCE) Product Catalog:
Products (19)
19 Results for "Human Adenovirus" in MCE Product Catalog:
28
28 Publications Verification
Synonyms: BW 759; 2'-Nor-2'-deoxyguanosine
Ganciclovir (BW 759), a nucleoside analogue, is an orally active antiviral agent with activity against CMV. Ganciclovir also has activity in vitro against members of the herpes group and some other DNA viruses. Ganciclovir inhibits the in vitro replication of human herpes viruses (HSV 1 and 2, CMV) and adenovirus serotypes 1, 2, 4, 6, 8, 10, 19, 22 and 28. Ganciclovir has an IC50 of 5.2 μM for feline herpesvirus type-1 (FHV-1) and can diffuse into the brain .
28
28 Publications Verification
Synonyms: BW 759 sodium; 2'-Nor-2'-deoxyguanosine sodium
Ganciclovir (BW 759) sodium, a nucleoside analogue, is an orally active antiviral agent with activity against CMV. Ganciclovir sodium also has activity in vitro against members of the herpes group and some other DNA viruses. Ganciclovir sodium inhibits the in vitro replication of human herpes viruses (HSV 1 and 2, CMV) and adenovirus serotypes 1, 2, 4, 6, 8, 10, 19, 22 and 28. Ganciclovir sodium has an IC50 of 5.2 μM for feline herpesvirus type-1 (FHV-1) and can diffuse into the brain .
5
5 Cited Publications
Target:
Braco-19 trihydrochloride is a potent telomerase/telomere inhibitor, preventing the capping and catalytic action of telomerase. Braco-19 acts as G-quadruplex (GQ) binding ligand, stabilizing G-quadruplexes formation at the 3V telomeric DNA overhang and produce rapid senescence or selective cell death. Braco-19 is also a HAdV virus replication inhibitor .
Cat. No.: HY-18944
CAS No.: 1113044-49-7
Target:
Research Areas:
FIT-039 is a selective, ATP-competitive and orally active CDK9 inhibitor with an IC50 of 5.8 μM for CKD9/cyclin T1. FIT-039 does not inhibit other CDKs and other kinases. FIT-039 inhibits replication of HSV-1 (IC50 of 0.69 μM), HSV-2, human adenovirus, and human CMV. FIT-039 is a promising antiviral agent for inhibiting drug-resistant HSVs and other DNA viruses.
Synonyms: Ingamine
Target:
Research Areas:
Ingavirin (Ingamine) exhibits broad spectrum antiviral activities against human respiratory viruses, such as influenza virus A (IVA), human parainfluenza virus (hPIV) and human adenovirus (AdV). Ingavirin exhibits no toxixcity to mice at the dose of 3000 mg/kg .
Synonyms: BW 759-d5; 2'-Nor-2'-deoxyguanosine-d5
Cat. No.: HY-13637R
CAS No.: 82410-32-0
Synonyms: BW 759 (Standard); 2'-Nor-2'-deoxyguanosine (Standard)
Ganciclovir (Standard) is the analytical standard of Ganciclovir. This product is intended for research and analytical applications. Ganciclovir (BW 759), a nucleoside analogue, is an orally active antiviral agent with activity against CMV. Ganciclovir also has activity in vitro against members of the herpes group and some other DNA viruses. Ganciclovir inhibits the in vitro replication of human herpes viruses (HSV 1 and 2, CMV) and adenovirus serotypes 1, 2, 4, 6, 8, 10, 19, 22 and 28. Ganciclovir has an IC50 of 5.2 μM for feline herpesvirus type-1 (FHV-1) and can diffuse into the brain .
Cat. No.: HY-P5407
CAS No.: 798569-33-2
Cat. No.: HY-P990861
Target:
Research Areas:
Cat. No.: HY-156786
CAS No.: 1471479-22-7
TLD-1433 is a ruthenium (II)-based water-soluble photodynamic compound. TLD-1433 inactivates enveloped viruses by inducing lipid peroxidation. TLD-1433 inactivates a variety of human pathogenic enveloped and non-enveloped viruses. TLD-1433 can be used in the research of viral infections and BCG-unresponsive non-muscle invasive bladder cancer .
Cat. No.: HY-13637B
CAS No.: 1359968-33-4
Synonyms: BW-759 hydrate; 2'-Nor-2'-deoxyguanosine hydrate
Ganciclovir (BW 759) hydrate, a nucleoside analogue, is an orally active antiviral agent with activity against CMV. Ganciclovir hydrate also has activity in vitro against members of the herpes group and some other DNA viruses. Ganciclovir hydrate inhibits the in vitro replication of human herpes viruses (HSV 1 and 2, CMV) and adenovirus serotypes 1, 2, 4, 6, 8, 10, 19, 22 and 28. Ganciclovir hydrate has an IC50 of 5.2 μM for feline herpesvirus type-1 (FHV-1) and can diffuse into the brain .
Cat. No.: HY-18944R
CAS No.: 1113044-49-7
Target:
Research Areas:
FIT-039 (Standard) is the analytical standard of FIT-039. This product is intended for research and analytical applications. FIT-039 is a selective, ATP-competitive and orally active CDK9 inhibitor with an IC50 of 5.8 μM for CKD9/cyclin T1. FIT-039 does not inhibit other CDKs and other kinases. FIT-039 inhibits replication of HSV-1 (IC50 of 0.69 μM), HSV-2, human adenovirus, and human CMV. FIT-039 is a promising antiviral agent for inhibiting drug-resistant HSVs and other DNA viruses.
Cat. No.: HY-13637AR
CAS No.: 107910-75-8
Synonyms: BW 759 sodium (Standard); 2'-Nor-2'-deoxyguanosine sodium (Standard)
Ganciclovir (sodium) (Standard) is the analytical standard of Ganciclovir (sodium). This product is intended for research and analytical applications. Ganciclovir (BW 759) sodium, a nucleoside analogue, is an orally active antiviral agent with activity against CMV. Ganciclovir sodium also has activity in vitro against members of the herpes group and some other DNA viruses. Ganciclovir sodium inhibits the in vitro replication of human herpes viruses (HSV 1 and 2, CMV) and adenovirus serotypes 1, 2, 4, 6, 8, 10, 19, 22 and 28. Ganciclovir sodium has an IC50 of 5.2 μM for feline herpesvirus type-1 (FHV-1) and can diffuse into the brain[1][2][3].
Cat. No.: HY-182341
CAS No.: 1261156-82-4
Target:
Research Areas:
APD-209 is a sialic acid conjugate with a PEG4 polar linker and a PDA non-polar tail. APD-209 aggregates adenovirus type 37 particles, blocks the binding of viral particles to human corneal epithelial cells, and inhibits cellular entry of adenovirus type 37. APD-209 can be used for the research of epidemic keratoconjunctivitis .
Cat. No.: HY-P70049
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: CXADR; CVB3-Binding Protein; CXADR Cell Adhesion Molecule; HCVADR; CAR; HCAR; Coxsackie Virus And Adenovirus Receptor; 46 KD Coxsackievirus And Adenovirus Receptor (CAR) Protein; Coxsackievirus And Adenovirus Receptor; CXADR, Ig-Like Cell Adhesion Molecul
Species:
Human
Source:
HEK293
Cat. No.: HY-P75471
Purity: ≥ 90%, as determined by reducing SDS-PAGE.
Synonyms: BNIP3L; NIP3L; BCL2 Interacting Protein 3 Like; BCL2/Adenovirus E1B 19-Kd Protein-Interacting Protein 3a; BNIP3a; BCL2/Adenovirus E1B 19kDa Interacting Protein 3-Like; Nix; Adenovirus E1B19k-Binding Protein B5; BCL2/Adenovirus E1B 19 KDa Protein-Interacti
Species:
Human
Source:
E. coli
Cat. No.: HY-P7670
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: BNIP3; BCL2/Adenovirus E1B 19kDa Interacting Protein 3; BCL2 Interacting Protein 3; BCL2/Adenovirus E1B Interacting Protein 3; HABON; Nineteen KD Interacting Protein-3; Nip3; CDNA FLJ60537, Highly Similar To BCL2/Adenovirus E1B 19 KDa Protein-Interacting
Species:
Human
Source:
E. coli
Cat. No.: HY-P7609
Purity: ≥ 95%, as determined by reducing SDS-PAGE.
Synonyms: CLMP; Adipocyte-Specific Adhesion Molecule; CXADR Like Cell Adhesion Molecule; Adipocyte Adhesion Molecule; ASAM; CXADR-Like Membrane Protein; ACAM; FLJ22415; Coxsackie- And Adenovirus Receptor-Like Membrane Protein; CSBM; CXADR Like Membrane Protein; CSB
Species:
Human
Source:
HEK293
Cat. No.: HY-P5407A
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Protocols
Targeted therapy! The Capetin Prize winning "Click Chemistry" can be used like this!Targeted therapy! The Nobel Prize winning "Click Chemistry" can be used like this!A suitable model is crucial in drug screening experiments. Organs can mimic the three-dimensional functional structure of internal organs, have similar spatial organization to corresponding organs, maintain some key characteristics, and reproduce some physiological functions. They are widely used for modeling and personalized drug screening physiological functions.2025-02-06
