254 Results for "

acyclovir

" in MedChemExpress (MCE) Product Catalog:
Products (254)

254 Results for "acyclovir" in MCE Product Catalog:

FM213
FM213
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製品番号: HY-P11891
Target:  

PD-1/PD-L1

研究分野:  

Cancer

FM213 is a PD-L1 inhibitor with a human IC50 of 323 nM. FM213 blocks PD-1/PD-L1 protein-protein interactions, and promotes endocytosis and lysosome-dependent degradation of PD-L1 on the surface of cancer cells. FM213 binds to PD-L1 on cancer cells and exosomes, and enhances the recognition and killing of cancer cells by human PBMC. Combination of FM213 with the TIGIT inhibitor DTBP-3 (HY-P11903) enhances anti-tumor immunity. FM213 can be used in research related to non-small cell lung cancer .
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tP4-CPP12
tP4-CPP12
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製品番号: HY-P11841
Target:  

DNA/RNA Synthesis

研究分野:  

Cancer

tP4-CPP12 is a RMI1/2 heterodimer inhibitor with an IC50 of 110 nM. tP4-CPP12 binds competitively at the FANCM-RMI interaction site and disrupts endogenous FANCM-RMI protein-protein interactions. tP4-CPP12 induces antiproliferative effects in ALT-positive osteosarcoma cells. tP4-CPP12 is applicable for the research of ALT-positive osteosarcoma .
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Nummularine B
Nummularine B
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製品番号: HY-P2209
CAS 番号: 53947-96-9
別名: Daechuine S27; N-Demethylamphibine H
Category:  

Alkaloids Other Alkaloids Plants Actaea simplex (DC.) Wormsk. ex Fisch. & C. A. Mey. Rhamnaceae

Target:  

Parasite Phosphodiesterase (PDE)

Nummularine B (Daechuine S27; N-Demethylamphibine H) is an anti-parasite agent. Nummularine B inhibits calmodulin-dependent phosphodiesterase activity with an IC50 of 16.8 μM. Nummularine B inhibits the growth of Plasmodium and Leishmania donovani in vitro. Nummularine B inhibits the calmodulin-dependent activity of actomyosin Ca 2+-ATPase. Nummularine B is applicable to research related to malaria and visceral leishmaniasis .
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Mycobacillin
Mycobacillin
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製品番号: HY-N14799
CAS 番号: 18524-67-9
Category:  

Microorganisms Antibiotics Other Antibiotics

Target:  

Antibiotic Fungal

Mycobacillin is a peptide antibiotic with anti-antifungal activity .
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Mp-4D7-pF2
Mp-4D7-pF2
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製品番号: HY-P11032
CAS 番号: 3106022-48-1
Target:  

SARS-CoV Virus Protease

研究分野:  

Infection

Mp-4D7-pF2, a cell-penetrating bicyclic peptide, is a noncovalent SARS-CoV-2 main protease inhibitor with an IC50 of 4.51 μM. Mp-4D7-pF2 has an antiviral activity against SARS-CoV-2 with no cytotoxicity. Mp-4D7-pF2 can used for COVID-19 infections research .
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TATE-DA-I
TATE-DA-I
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製品番号: HY-P11924
Target:  

Somatostatin Receptor Drug Intermediate

研究分野:  

Cancer

TATE-DA-I is a somatostatin receptor 2 (SSTR2) ligand with an IC50 of 25.3 nM. TATE-DA-I binds to albumin to prolong its circulation retention time and also exhibits enhanced tumor accumulation capacity. TATE-DA-I enables clear visualization of SSTR2-positive tumors in SPECT/CT imaging. TATE-DA-I can be used in cancer-related research .
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TAK 044
TAK 044
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製品番号: HY-105168
CAS 番号: 157380-72-8
Target:  

Endothelin Receptor

研究分野:  

Cardiovascular Disease

TAK 044 is an antagonist of Endothelin Receptor. TAK 044 strongly inhibits ET-induced deterioration in various animal models. TAK 044 can be used in study ET-related diseases such as acute myocardial infarction,acute renal failure, acute hepatic malfunction, and subarachnoid hemorrhage .
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JR11-PEG3-DOTA-PSMA-03
JR11-PEG3-DOTA-PSMA-03
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製品番号: HY-P11488
Target:  

Radionuclide-Drug Conjugates (RDCs) Somatostatin Receptor PSMA

研究分野:  

Cancer

JR11-PEG3-DOTA-PSMA-03 (Compound 2) is an RDC-related compound containing the chelating agent DOTA (HY-W053583), the JR11 peptide (SSTR2 antagonist), and the PSMA ligand. JR11-PEG3-DOTA-PSMA-03 shows SSTR2-binding affinities and PSMA-binding affinities, with IC50 s of 94.0 nM, 81.8 nM, respectively. JR11-PEG3-DOTA-PSMA-03 can be radiolabeled with [ 68Ga]. [ 68Ga] radiolabeled JR11-PEG3-DOTA-PSMA-03 can be used in diagnostic studies of neuroendocrine differentiated prostate cancer .
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JR11-PEG3-HBED-CC-PSMA-03
JR11-PEG3-HBED-CC-PSMA-03
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製品番号: HY-P11485
Target:  

Radionuclide-Drug Conjugates (RDCs) Somatostatin Receptor PSMA

研究分野:  

Cancer

JR11-PEG3-HBED-CC-PSMA-03 (Compound 1) is an RDC-related compound containing the chelating agent HBED-CC, the JR11 peptide (SSTR2 antagonist), and the PSMA ligand. JR11-PEG3-HBED-CC-PSMA-03 shows SSTR2-binding affinities and PSMA-binding affinities, with IC50 s of 59.2 nM, 57.0 nM, respectively. JR11-PEG3-HBED-CC-PSMA-03 can be radiolabeled with [ 68Ga]. [ 68Ga] radiolabeled JR11-PEG3-HBED-CC-PSMA-03 can be used in diagnostic studies of neuroendocrine differentiated prostate cancer .
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Ternatin
Ternatin
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製品番号: HY-125357
CAS 番号: 148619-41-4
Target:  

阻害性抗体

研究分野:  

Metabolic Disease

Ternatin (compound 2) is a cyclic heptapeptides that can be isolated from mushroom Coliorus versicolor. Ternatin inhibits fat-accumulation with an IC50 of 0.027 μM in 3T3-L1 adipocytes .
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Omphalotin A
Omphalotin A
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製品番号: HY-P5957
CAS 番号: 186511-50-2
Category:  

Microorganisms Cyclopeptides

Target:  

Parasite

Omphalotin A is a cyclic peptide, and shows nematicidal activity .
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WL12
WL12
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製品番号: HY-P3440
CAS 番号: 1886057-64-2
Target:  

Radionuclide-Drug Conjugates (RDCs) PD-1/PD-L1

研究分野:  

Cancer

WL12 is a specifically targeting programmed death ligand 1 (PD-L1) binding peptide. WL12 can be radiolabeled by different radionuclides, generating radiotracers, which can assess the tumor PD-L1 expression .
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BiS3
BiS3
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製品番号: HY-P11927
Target:  

GSK-3

研究分野:  

Cancer

BiS3 is a selective hyperbivalent macrocyclic peptide GSK3β inhibitor, with a Kd of 0.28 nM and an IC50 of 4.8 nM against GSK3β. BiS3 is applicable to studies related to GSK3β signaling and colorectal cancer .
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Coumarin-Phalloidin
Coumarin-Phalloidin
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製品番号: HY-P4948
CAS 番号: 1926163-49-6
Target:  

Biochemical Assay Reagents

研究分野:  

Others

Coumarin-phalloidin is a kind of phalloidin labeled with Coumarin (HY-N0709). Coumarin-phalloidin is a new type of actin probe that can be used for triple immunofluorescence microscopic observation of the cell skeleton .
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Assay Types