Search Result

Results for "

Adenovirus

" in MCE Product Catalog:

By Targets:	Antibiotic (4) Apoptosis (1) ATP Synthase (1) Bacterial (1) CDK (1) CMV (8) DNA/RNA Synthesis (6) EBV (1) Endogenous Metabolite (1) Fungal (1) HIV (2) HPV (1) HSV (6) Isotope-Labeled Compounds (1) Nucleoside Antimetabolite/Analog (4) Orthopoxvirus (1) Parasite (1) Virus Protease (1)
By Research Areas:	Cancer (7) Infection (13)

Inhibitors & Agonists

Biochemical Assay Reagents

Natural
Products

Recombinant Proteins

Isotope-Labeled Compounds

Antibodies

Cat. No.	Product Name	Target	Research Areas

HY-I0660

Picolinic acid
PCL 016
Endogenous Metabolite Virus Protease Infection

Picolinic acid (PCL 016) is a topical antiviral agent, which inhibits adenovirus replication in rabbits.

Picolinic acid PCL 016	Endogenous Metabolite Virus Protease	Infection
Picolinic acid (PCL 016) is a topical antiviral agent, which inhibits adenovirus replication in rabbits.

HY-119098

GSK983	EBV HPV	Infection
GSK983 is a broad-spectrum antiviral agent. GSK983 inhibits the replication of adenovirus-5 (Ad-5) and polyoma virus SV40. GSK983 inhibits the growth of cell lines immortalized by EBV, HTLV1, HPV. GSK983 induces the expression of interferon-stimulated genes.

HY-17594

Oxyclozanide	Parasite Bacterial Fungal	Infection
Oxyclozanide is an orally active salicylanilide anthelmintic agent that mainly acts by uncoupling oxidative phosphorylation in flukes. Oxyclozanide shows good anti-adenovirus, anti-biofilm, antifungal, and antibacterial activity.

HY-N8533

Sodium Camptothecin	DNA/RNA Synthesis	Cancer Infection
Sodium Camptothecin is a plant alkaloid, with antitumor activity. Sodium Camptothecin is a reversible inhibitor of RNA synthesis. Sodium Camptothecin is an effective inhibitor of adenovirus replication. Sodium Camptothecin inhibits DNA synthesis and causes breaks in intracellular preformed viral DNA.

HY-128036

ddATP 2',3'-Dideoxyadenosine 5'-triphosphate	DNA/RNA Synthesis HIV	Infection
ddATP (2',3'-Dideoxyadenosine 5'-triphosphate), an active metabolite of 2',3'-dideoxyinosine, is a chain-elongating inhibitor of DNA polymerase. ddATP can be used for Sanger method for DNA sequencing and research of virus infection.

HY-128036B

ddATP trisodium 2',3'-Dideoxyadenosine 5'-triphosphate trisodium	DNA/RNA Synthesis HIV	Infection
ddATP (2',3'-Dideoxyadenosine 5'-triphosphate) trisodium, an active metabolite of 2',3'-dideoxyinosine, is a chain-elongating inhibitor of DNA polymerase. ddATP trisodium can be used for Sanger method for DNA sequencing and research of virus infection.

HY-126679

Apoptolidin	ATP Synthase Apoptosis	Cancer
Apoptolidin is a polyketide isolated from Nocardiopsis bacteria. Apoptolidin is a selective mitochondrial F₁F_O ATPase inhibitor. Apoptolidin is an apoptosis inducer and induces apoptotic cell death in cells transformed with the adenovirus type 12 oncogenes including ElA (IC₅₀=10-17 ng/ml) but not in normal cells.

HY-18944

FIT-039	CDK HSV CMV DNA/RNA Synthesis	Infection
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.

HY-14532

Brincidofovir CMX001; HDP-CDV	CMV HSV Orthopoxvirus	Infection
Brincidofovir (CMX001), the lipid-conjugated prodrug of Cidofovir (HY-17438), is an orally available, long-acting antiviral. Brincidofovir shows activity against a broad spectrum of DNA viruses including cytomegalovirus (CMV), adenovirus (ADV), varicella zoster virus, herpes simplex virus, polyomaviruses, papillomaviruses, poxviruses, and mixed double-stranded DNA virus infections. Brincidofovir, an oral antiviral in late stage development, has proven effective against orthopoxviruses in vitro and in vivo..

HY-13637B

Ganciclovir hydrate BW-759 hydrate; 2'-Nor-2'-deoxyguanosine hydrate	CMV HSV Antibiotic Nucleoside Antimetabolite/Analog	Cancer Infection
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.

HY-13637

Ganciclovir BW 759; 2'-Nor-2'-deoxyguanosine	CMV HSV Antibiotic Nucleoside Antimetabolite/Analog	Infection Cancer
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.

HY-13637A

Ganciclovir sodium BW 759 sodium; 2'-Nor-2'-deoxyguanosine sodium	CMV HSV Antibiotic Nucleoside Antimetabolite/Analog	Infection Cancer
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.

HY-13637S

Ganciclovir-d5 BW 759-d₅; 2'-Nor-2'-deoxyguanosine-d₅	Isotope-Labeled Compounds CMV HSV Antibiotic Nucleoside Antimetabolite/Analog	Infection
Ganciclovir-d₅ is the deuterium labeled Ganciclovir. 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)[1][2][3].

HY-15523

Braco-19	CMV DNA/RNA Synthesis	Cancer
Braco-19 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.

HY-15523A

Braco-19 trihydrochloride	DNA/RNA Synthesis CMV	Cancer Infection
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.	Product Name	Type

HY-128036

ddATP 2',3'-Dideoxyadenosine 5'-triphosphate	Gene Sequencing and Synthesis
ddATP (2',3'-Dideoxyadenosine 5'-triphosphate), an active metabolite of 2',3'-dideoxyinosine, is a chain-elongating inhibitor of DNA polymerase. ddATP can be used for Sanger method for DNA sequencing and research of virus infection.

Cat. No.	Product Name	Target	Category

HY-I0660

Picolinic acid PCL 016	Endogenous Metabolite Virus Protease	Ketones, Aldehydes, Acids Structural Classification Nervous System Disorder Endogenous metabolite Disease markers Source classification Infection Disease Research Fields Anti-aging Classification of Application Fields
Picolinic acid (PCL 016) is a topical antiviral agent, which inhibits adenovirus replication in rabbits.

HY-N8533

Sodium Camptothecin	DNA/RNA Synthesis	Alkaloids Quinoline Alkaloids Pyrrole Alkaloids Classification of Application Fields Disease Research Fields Infection Source classification Plants Nyssaceae Camptotheca acuminata Decne.
Sodium Camptothecin is a plant alkaloid, with antitumor activity. Sodium Camptothecin is a reversible inhibitor of RNA synthesis. Sodium Camptothecin is an effective inhibitor of adenovirus replication. Sodium Camptothecin inhibits DNA synthesis and causes breaks in intracellular preformed viral DNA.

HY-126679

Apoptolidin	ATP Synthase Apoptosis	Natural Products Disease Research Fields Cancer Source classification Microorganisms
Apoptolidin is a polyketide isolated from Nocardiopsis bacteria. Apoptolidin is a selective mitochondrial F₁F_O ATPase inhibitor. Apoptolidin is an apoptosis inducer and induces apoptotic cell death in cells transformed with the adenovirus type 12 oncogenes including ElA (IC₅₀=10-17 ng/ml) but not in normal cells.

Species:	Human (3) Mouse (2)
Tag:	His (3) Tag Free (1) Avi (1) Fc (1)
Source:	HEK293 (3) E. coli (2)

Cat. No.	Product Name	Species	Source

HY-P70049

CXADR Protein, Human (HEK293, His) rHuCoxsackievirus and Adenovirus receptor/CXADR, His ; Coxsackievirus and Adenovirus Receptor; CAR; hCAR; CVB3-Binding Protein; Coxsackievirus B-Adenovirus Receptor; HCVADR; CXADR; CAR	Human	HEK293

HY-P70052

CXADR Protein, Mouse (HEK293, Fc)
rMuCoxsackievirus and Adenovirus receptor homolog/CXADR, Fc; Coxsackievirus and Adenovirus receptor homolog; CAR; Cxadr; CVB3 BP
Mouse HEK293
HY-P72364

CXADR Protein, Mouse (Biotinylated, HEK293, Avi-His)
Coxsackievirus and Adenovirus receptor homolog; CAR; Cxadr; CVB3 BP
Mouse HEK293

HY-P7670

BNIP3/NIP3 Protein, Human (His) rHuBNIP3, His; BNIP3; NIP3; BCL2/Adenovirus E1B 19 kDa Protein-Interacting Protein 3	Human	E. coli
BNIP3/NIP3 Protein, Human (His) expresses in E. coliwith a His tag. BNIP3 belongs to the Bcl-2 protein family that regulates programmed cell death.

HY-P75471

BNIP3L Protein, Human
BCL2/Adenovirus E1B 19 kDa protein-interacting protein 3-like; NIP3L; BNIP3L; BNIP3A; BNIP3H; NIX
Human E. coli

Cat. No.	Product Name

HY-13637S

Ganciclovir-d5
Ganciclovir-d₅ is the deuterium labeled Ganciclovir. 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)[1][2][3].

Ganciclovir-d5

Ganciclovir-d₅ is the deuterium labeled Ganciclovir. 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)[1][2][3].

Cat. No.	Product Name	Application	Reactivity

HY-P80571

BNIP3L Antibody Adenovirus E1B19k binding protein B5; BNIP3a; BNIP3H; BNIP3L; BNIP3L protein; NIP3 like protein X; NIP3L; NIX	WB, IHC-P	Human, Mouse, Rat
BNIP3L Antibody is a non-conjugated and Rabbit origined polyclonal antibody about 24 kDa, targeting to BNIP3L. It can be used for WB,IHC-P assays with tag free, in the background of Human, Mouse, Rat.