22 Results for "

4-Iodophenyl bromide-13C6

" in MedChemExpress (MCE) Product Catalog:
Products (22)

22 Results for "4-Iodophenyl bromide-13C6" in MCE Product Catalog:

1
1 Cited Publications
Cat. No.: HY-I0198
CAS No.: 385425-15-0
Synonyms: 1-(4-Iodophenyl)piperidin-2-one
Target:  

Drug Intermediate

Research Areas:  

Others

1-(4-Iodophenyl)-2-piperidinone (1-(4-Iodophenyl)piperidin-2-one) is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-W171304
CAS No.: 1528991-21-0
Target:  

Ligands for E3 Ligase

Research Areas:  

Cancer

Hydrouracil-4-Iodophenyl is an E3 ubiquitin ligase cereblon (CRBN) ligand used to recruit the cereblon protein. Hydrouracil-4-Iodophenyl can be linked to a target protein ligand via a linker to form a PROTAC.
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Cat. No.: HY-W104869
CAS No.: 1643-29-4
Target:  

PROTAC Linkers

Research Areas:  

Cancer

3-(4-Iodophenyl)propanoic acid is a PROTAC linker that can be used in the synthesis of PROTACs.
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Cat. No.: HY-66016
CAS No.: 885588-03-4
Target:  

Drug Intermediate

Research Areas:  

Others

3-[(2-Fluoro-4-iodophenyl)amino]isonicotinic acid is a drug intermediate for synthesis of various active compounds.
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Cat. No.: HY-P10563
CAS No.: 2580150-96-3
Synonyms: BHV-1100
Target:  

CD38 IFNAR

Research Areas:  

Cancer

Noraramtide (BHV-1100) is an antibody-recruiting molecule. Noraramtide binds to CD38 and recruits natural killer (NK) cells to mediate antibody-dependent cellular cytotoxicity. Noraramtide enhances the capacity of autologous cytokine-induced memory-like (CIML) NK cells to produce IFNγ and CD107a, thereby improving their cytotoxicity against multiple myeloma cells. Noraramtide can be used in the research of multiple myeloma .
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Cat. No.: HY-P3350
CAS No.: 2892148-58-0
Target:  

Bacterial

Research Areas:  

Infection

LS-BF1 is a stable and low toxic cationic antimicrobial peptide. LS-BF1 displays broad spectrum of antibacterial activity, including the challenging ESKAPE pathogens, by cell membrane disruptive mechanism. LS-BF1 shows good in vivo efficacy for elimination of bacteria in a mouse infection model[1].
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Cat. No.: HY-W013964
CAS No.: 39959-59-6
Synonyms: (4-Iodophenyl)methanamine
Research Areas:  

Others

4-Iodobenzylamine ((4-Iodophenyl)methanamine) is a probe that can detect the binding patterns of serine proteases that are like trypsin, as well as urokinase-type plasminogen activator (uPA). 4-Iodobenzylamine is stable in aqueous solution .
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Cat. No.: HY-W248119
CAS No.: 250734-47-5
8-(4-Iodophenyl)-1,3,5,7-tetramethyl BODIPY is a BODIPY derivative that can be used as a fluorescent probe for GFP-labeled muscarinic M1 receptor .
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Cat. No.: HY-P3567
CAS No.: 159600-82-5
Target:  

Melanocortin Receptor

Research Areas:  

Neurological Disease

(p-Iodo-Phe7)-ACTH (4-10) is a adrenocorticotrophic hormone (ACTH) derivative, which is produced and secreted by the anterior pituitary gland. (p-Iodo-Phe7)-ACTH (4-10) serves as a melanocortin (MC) receptor antagonist and inhibits α-melanocyte-stimulating hormone (α-MSH)-induced excessive grooming behavior in rats .
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Cat. No.: HY-P2434
CAS No.: 846569-60-6
AP102 is a dual SSTR2/SSTR5-specific somatostatin analog (SSA). AP102 is a disulfide-bridged octapeptide SSA containing synthetic iodinated amino acids. AP102 binds with subnanomolar affinity to SSTR2 and SSTR5 (IC50: 0.63 and 0.65 nM, respectively). AP102 does not bind to SSTR1 or SSTR3. AP102 can be used for acromegaly and neuroendocrine tumors research .
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Cat. No.: HY-105168
CAS No.: 157380-72-8
Target:  

Endothelin Receptor

Research Areas:  

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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Cat. No.: HY-141919S
CAS No.: 1261170-84-6
Synonyms: 4-Iodobromobenzene-13C6; 4-Iodophenyl bromide-13C6; NSC 8033-13C6
1-Bromo-4-iodobenzene- 13C6 is the 13C labeled 1-Bromo-4-iodobenzene .
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Cat. No.: HY-D1486
CAS No.: 216255-54-8
4,4-Difluoro-8-(4'-iodophenyl)-1,7-bis-(1'-napthyl)-4-bora-3alpha,4alpha-diaza-s-indacene is a fluorescent dye for DNA sequencing .
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Cat. No.: HY-W104868
CAS No.: 59528-27-7
Research Areas:  

Others

4-Iodobenzylamine hydrochloride ((4-Iodophenyl)methanamine hydrochloride) is a probe that can detect the binding patterns of serine proteases that are like trypsin, as well as urokinase-type plasminogen activator (uPA) .
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Cat. No.: HY-W456568
CAS No.: 29162-74-1
Target:  

MOFs

Research Areas:  

Others

5,10,15,20-Tetrakis(4-iodophenyl)porphyrin (5,10,15,20-tetrakis(4-iodophenyl)porphyrin) is a metal-organic framework (MOF).
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Cat. No.: HY-W112379
CAS No.: 60095-56-9
Target:  

MOFs

Research Areas:  

Others

1,1'-Bis(4-iodophenyl)-[4,4'-bipyridine]-1,1'-diiumchloride is a metal-organic framework (MOF).
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Cat. No.: HY-W112961
CAS No.: 934008-48-7
Synonyms: 1,3-Bis(2,6-diisopropyl-4-Iodophenyl)imidazolium chloride
Target:  

MOFs

Research Areas:  

Others

1,3-Bis(4-iodo-2,6-diisopropylphenyl)-1H-imidazol-3-iumchloride(1,3-Bis(2,6-diisopropyl-4-iodophenyl)imidazolium chloride) is a metal-organic framework (MOF).
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Cat. No.: HY-W543735
CAS No.: 2607030-32-8
Target:  

MOFs

Research Areas:  

Others

1,3-Bis-(4-iodo-phenyl)-3H-imidazol-1-ium;bromide is a metal-organic framework (MOF).
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Cat. No.: HY-188067
CAS No.: 497180-72-0
Target:  

Imidazoline Receptor

Research Areas:  

Cardiovascular Disease

LNP-911 is a ligand for the I1 imidazoline receptor. LNP-911 allosterically modulates I1Rs and enhances the effect of agonists on Forskolin (HY-15371)-stimulated cAMP accumulation. LNP-911 exists mainly as a stable imine tautomer. After radioiodination, LNP-911 serves as a selective high-affinity radioligand for characterization studies of I1Rs in membrane preparations. LNP-911 can be used in hypertension-related research .
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Cat. No.: HY-P1981
CAS No.: 157381-54-9
Target:  

HIV Protease

Research Areas:  

Infection Inflammation/Immunology

Rpi-856 A is a competitive inhibitor of HIV-1 protease and HTLV-I protease, with an IC50 of 37 nM against HIV-1 protease and an IC50 of 27 nM against HTLV-I protease. Rpi-856 A inhibits Pepsin with an IC50 of 1.9 μM . Rpi-856 A does not inhibit chymosin, trypsin, chymotrypsin, papain, bromelain, thermolysin, prolyl endopeptidase, carboxypeptidase A or carboxypeptidase B. Rpi-856 A can be used in the research of acquired immunodeficiency syndrome (AIDS) and related diseases, as well as HIV infection .
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