316 Results for "

PR

" in MedChemExpress (MCE) Product Catalog:
Products (316)

316 Results for "PR" in MCE Product Catalog:

Cat. No.: HY-P99852
CAS No.: 1791420-09-1
Synonyms: ABT165; PR1283233

Target:  

VEGFR Notch

Research Areas:  

Cancer

Dilpacimab (ABT165) is a bispecific variable domain immunoglobulin. Dilpacimab binds to and inhibits DLL4 and VEGF and acts as a tumor growth inhibitor. Dilpacimab can be used in research related to metastatic colorectal cancer and advanced solid tumors .
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Cat. No.: HY-16405
CAS No.: 851627-62-8
Research Areas:  

Cancer

PR-104 is a selective hypoxia-activated DNA cross-linking agent and can be used for the research of multiple tumor xenograft models. PR-104, as a nitrogen mustard pre-proagent, is converted efficiently to the more lipophilic dinitrobenzamide mustards alcohol PR-104A .
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Cat. No.: HY-126145
CAS No.: 2328109-05-1
Purity:  99.52%
Target:  

LPL Receptor

Research Areas:  

Inflammation/Immunology

S1PR1 modulator 1 is a selective S1PR1 inhibitor, with a pIC50 of 7.6, with >40- and >80-fold selectivity, over the other S1PR isoforms S1PR2/3/4 .
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Cat. No.: HY-109963
CAS No.: 1005307-86-7
Purity:  98.45%
Research Areas:  

Cancer

PR5-LL-CM01 is a potent protein arginine methyltransferase 5 (PRMT5) inhibitor (IC50= 7.5 μM). Anti-tumor activies .
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Cat. No.: HY-11028
CAS No.: 936345-35-6
Purity:  99.88%
Synonyms: PF-2413873
Target:  

Progesterone Receptor

Research Areas:  

Endocrinology

PF-02413873 (PF-2413873) is a potent selective, fully competitive and orally active nonsteroidal progesterone receptor (PR) antagonist, with a Ki of 2.6 nM. PF-02413873 can block progesterone binding and PR nuclear translocation, and inhibit endometrial growth in vivo .
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Cat. No.: HY-P10697A
Target:  

LDLR

Research Areas:  

Metabolic Disease

VH4127 TFA is a cyclic peptide targeting the low density lipoprotein receptor (LDLR) with a KD of 18 nM for hLDLR. VH4127 TFA specifically binds to rodent and human epidermal growth factor (EGF) homology domain of LDLR .
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Cat. No.: HY-14572
CAS No.: 680199-06-8
Synonyms: SN 27858
Research Areas:  

Cancer

PR-104A (SN 27858) is the alcohol metabolite of phosphate proagent PR-104. PR-104A is a hypoxia-selective DNA cross-linking agent/DNA-damaging agent and cytotoxin. Antitumor Activity . PR-104A is metabolized under hypoxia by the 1-electron NADPH:cytochrome P450 oxidoreductase. PR-104A can be used for the research of relapsed/refractory T-lineage acute lymphoblastic leukemia (T-ALL) .
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Cat. No.: HY-10455R
CAS No.: 868540-17-4
Synonyms: PR-171 (Standard)
Research Areas:  

Cancer

Carfilzomib (Standard) is the analytical standard of Carfilzomib. This product is intended for research and analytical applications. Carfilzomib (PR-171) is an irreversible proteasome inhibitor with an IC50 of 5 nM in ANBL-6 and RPMI 8226 cells.
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Cat. No.: HY-P1788
CAS No.: 132326-73-9
Target:  

Influenza Virus

Research Areas:  

Infection

Influenza A NP(366-374) Strain A/PR/8/35 is an H2-Db-restricted epitope from Influenza A/PR/8/35 nucleoprotein .
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Cat. No.: HY-P990827

Target:  

TROP2

Research Areas:  

Cancer

Anti-TROP-2 Antibody (Pr1E11) is a kind of mouse IgG1 κ chimeric antibody inhibitor, targeting to human TROP-2. Anti-TROP-2 Antibody (Pr1E11) specifically binds to TROP-2 with high affinity and shows low internalization activitv. Anti-TROP-2 Antibody (Pr1E11) can be used for the research of cancer, such as epithelial cancer and primary pancreatic cancer .
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Cat. No.: HY-P990904
CAS No.: 2837169-12-5
Synonyms: PR-1925514

Target:  

CCR

Research Areas:  

Inflammation/Immunology

HY-P990904 is an CCR8-targeting IgG1κ type humanized antibody, the recommed isotype control is Human IgG1 kappa, Isotype Control (HY-P99001) .
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Cat. No.: HY-157493
CAS No.: 936345-34-5
Target:  

Progesterone Receptor

Research Areas:  

Endocrinology

PR antagonist 1 (compound 8) is a selective progesterone receptor (PR) antagonist, and can be used for the research of a variety of progesterone-related diseases and disorders such as endometriosis and uterine fibroids .
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Cat. No.: HY-W873634
CAS No.: 1242003-07-1
Synonyms: TRAP-PR
Research Areas:  

Cancer

TRAP-Pr is a radionuclide conjugate (RDC) that can bind to the radionuclide [68]Ga. RDCs have the ability to specifically target biomolecules and can be used in medical imaging or therapy. TRAP-Pr can be further functionalized with acetone and used in click chemistry CuAAC reactions to conjugate other labeled molecules.
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Cat. No.: HY-RS12391
Research Areas:  

Others

S1PR1 Human Pre-designed siRNA Set A contains three designed siRNAs for S1PR1 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-160604
CAS No.: 128298-28-2
Synonyms: FPL 12924; PR 934-423; FPL 13592
Target:  

iGluR

Research Areas:  

Neurological Disease

Remacemide (FPL 12924) is an orally active, non-competitive, low-affinity NMDA receptor antagonist. Remacemide shows neuroprotection activity in animal models of hypoxia and ischemic stroke. Remacemide is also an anticonvulsant, and can be used in Parkinson's disease and Huntington's disease research .
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Cat. No.: HY-P1259
CAS No.: 139637-11-9
Target:  

Proteasome Bacterial

Research Areas:  

Inflammation/Immunology

PR-39, a natural proline- and arginine-rich antibacterial peptide, is a noncompetitive, reversible and allosteric proteasome inhibitor. PR-39 reversibly binds to the α7 subunit of the proteasome and blocks degradation of NF-κB inhibitor IκBα by the ubiquitin-proteasome pathway. PR-39 stimulates angiogenesis, inhibits inflammatory responses and significant reduces myocardial infarct size in mice .
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Cat. No.: HY-106827
CAS No.: 74513-62-5
Synonyms: RU 27987
Trimegestone (RU 27987) is an orally active, selective progestogen and PR ligand, with an IC50 of 7.6 nM for hPR, 4.4 nM for rabbit PR, and 3.3 nM for rat PR. Trimegestone induces Alkaline phosphatase activity. Trimegestone exhibits antiandrogenic activity (IC50 = 303 nM). Trimegestone can be used in research related to menopausal symptoms and osteoporosis .
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Cat. No.: HY-126484
CAS No.: 60048-73-9
Eremofortin B is a sesquiterpenoid compound synthesized by penicillium roqueforti PR Toxin (PRT) .
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Cat. No.: HY-RS12394
Research Areas:  

Others

S1PR2 Human Pre-designed siRNA Set A contains three designed siRNAs for S1PR2 gene (Human), as well as a negative control, a positive control, and a FAM-labeled negative control.

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Cat. No.: HY-P99892
CAS No.: 2140172-41-2
Synonyms: PR-1594407; DC-1630423

Target:  

EGFR

Research Areas:  

Others

Serclutamab is a humanized chimeric antibody targeting EGFR IgG1-κ. Mainly expressed by CHO (Chinese Hamster Ovary) cells .
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