218 Results for "

macrocyclic

" in MedChemExpress (MCE) Product Catalog:
Products (218)

218 Results for "macrocyclic" in MCE Product Catalog:

115
115 Publications Verification
Art. -Nr.: HY-13756
CAS. Nr.: 104987-11-3
Reinheit:  99.93%
Synonyms: FK506; Fujimycin; FR900506
Tacrolimus (FK506), a molecular glue, a macrocyclic lactone, binds to FK506 binding protein (FKBP) to form a complex. Tacrolimus inhibits calcineurin phosphatase, which inhibits T-lymphocyte signal transduction and IL-2 transcription. Immunosuppressive properties .
loading...
    loading...
115
115 Publications Verification
Art. -Nr.: HY-13756A
CAS. Nr.: 109581-93-3
Reinheit:  99.67%
Synonyms: FK506 monohydrate; Fujimycin monohydrate; FR900506 monohydrate
Tacrolimus (FK506) monohydrate, a molecular glue, a macrocyclic lactone, binds to FK506 binding protein (FKBP) to form a complex. Tacrolimus monohydrate inhibits calcineurin phosphatase, which inhibits T-lymphocyte signal transduction and IL-2 transcription. Immunosuppressive properties .
loading...
    loading...
51
51 Cited Publications
Art. -Nr.: HY-N0750
CAS. Nr.: 315-22-0
Synonyms: Crotaline
Monocrotaline is an 11-membered macrocyclic pyrrolizidine alkaloid. Monocrotaline inhibits OCT-1 and OCT-2 with IC50s of 36.8 µM and 1.8 mM, respectively. Monocrotaline has antitumor activity and is cytotoxic to hepatocellular carcinoma cells. Monocrotaline is used to induce a model of pulmonary hypertension in rodents. [2][6][8].
loading...
    loading...
10
10 Cited Publications
Art. -Nr.: HY-N6693
CAS. Nr.: 2001-95-8
Synonyms: NSC 122023
Valinomycin is a potassium-specific ionophore, the valinomycin-K + complex can be incorporated into biological bilayer membranes with the hydrophobic surface of valinomycin, destroys the normal K + gradient across the membrane, and as a result kills the cells, incorporating into liposomes can significantly reduces the cytotoxicity and enhances the targeting effect. Valinomycin exhibits antibiotic, antifungal, antiviral, antitumor and insecticidal efficacy, thus can be used for relevant research .
loading...
    loading...
9
9 Cited Publications
Art. -Nr.: HY-15739
CAS. Nr.: 66584-72-3
Reinheit:  ≥98.0%
Synonyms: Antibiotic C 15003P3; Maytansinol isobutyrate
Ansamitocin P-3 (Antibiotic C 15003P3) is a microtubule inhibitor. Ansamitocin P-3 is a macrocyclic antitumor antibiotic.
loading...
    loading...
7
7 Cited Publications
Art. -Nr.: HY-17580
CAS. Nr.: 873857-62-6
Synonyms: OPT-80; PAR-101
Fidaxomicin (OPT-80), a macrocyclic antibiotic, is an orally active and potent RNA polymerase inhibitor. Fidaxomicin has a narrow spectrum of antibacterial activity and a good anti-Clostridium difficile activity (MIC90=0.12 μg/mL). Fidaxomicin can be used for Clostridium difficile infection (CDI) research .
loading...
    loading...
6
6 Cited Publications
Art. -Nr.: HY-13557
CAS. Nr.: 104987-12-4
Reinheit:  ≥98.0%
Synonyms: Immunomycin; FR-900520; FK520
Ascomycin (Immunomycin; FR-900520; FK520) is an ethyl analog of Tacrolimus (FK506) with strong immunosuppressant properties. Ascomycin is also a macrocyclic polyketide antibiotic with multiple biological activities such as anti-malarial, anti-fungal and anti-spasmodic. Ascomycin prevents graft rejection and has potential for varying skin ailments research .
loading...
    loading...
5
5 Cited Publications
Art. -Nr.: HY-17566
CAS. Nr.: 1405-37-4
Capreomycin sulfate is a macrocyclic peptide antibiotic that inhibits phenylalanine synthesis in mycobacterial ribosomal translation. Capreomycin sulfate has anti-amyloidogenic and pro-fibrinolytic activities, reducing amyloid-induced cytotoxicity by inhibiting the occurrence of amyloid fibrillation. Capreomycin sulfate can be used in the study of multidrug-resistant tuberculosis, type 2 diabetes, Alzheimer's disease and Parkinson's disease .
loading...
    loading...
3
3 Cited Publications
Art. -Nr.: HY-N6686
CAS. Nr.: 21411-53-0
Synonyms: Pristinamycin IIA; Ostreogrycin A
Virginiamycin M1 (Pristinamycin IIA; Ostreogrycin A), produced by?Streptomyces virginiae, is an polyunsaturated macrocyclic lactone antibiotic and acts as a component of Virginiamycin (HY-112665) . Virginiamycin M1 alone is against Staphylococcus aureus with a MIC of 0.25 μg/mL.
loading...
    loading...
3
3 Cited Publications
Art. -Nr.: HY-W053583
CAS. Nr.: 60239-18-1
Synonyms: DOTA
Tetraxetan (DOTA) is a macrocyclic chelating agent. Tetraxetan can form stable coordination complexes with a variety of metal ions (e.g., 68Ga, 111In, 177Lu). Tetraxetan can be conjugated with targeting molecules (e.g., RGD peptide, folic acid) to enable the complex to target specific biomolecules or cells. Tetraxetan can be used for imaging studies of tumors, including melanoma and folate receptor-positive tumors (e.g., cervical cancer) .
loading...
    loading...
1
1 Cited Publications
Art. -Nr.: HY-122402
CAS. Nr.: 851536-75-9
Reinheit:  99.35%
Target:  

Bacterial

Forschungsgebiete:  

Inflammation/Immunology

Umirolimus, a macrocyclic triene lactone Rapamycin derivative, is powerful immunosuppressant and anti-inflammatory agent. Umirolimus has highly lipophilicity and can be used agent-eluting stent (DES) applications .
loading...
    loading...
1
1 Cited Publications
Art. -Nr.: HY-D0179
CAS. Nr.: 295-37-4
Forschungsgebiete:  

Cancer

Cyclam is a macrocyclic polyamine that can serve as a high-affinity chelator for Cu2+ and a CXCR4-targeting motif. Cyclam is the CXCR4-binding unit of the CXCR4 antagonist Plerixafor (AMD3100) (HY-10046). Cyclam-based macrocyclic compounds possess anti-HIV activity and can mobilize stem cells from the bone marrow. Cyclam can be used in research on ovarian cancer with high CXCR4 expression, as well as in the development of Cu 2+ sensors and lanthanide luminescent bioprobes .
loading...
    loading...
1
1 Cited Publications
Art. -Nr.: HY-P5963
CAS. Nr.: 2983116-47-6
Target:  

Interleukin Related

Forschungsgebiete:  

Inflammation/Immunology

Lib2-1, a macrocyclic peptide, is an IL-17C/IL-17RE interaction inhibitor. Lib2-1 can be used for autoimmune and inflammatory diseases research .
loading...
    loading...
1
1 Cited Publications
Art. -Nr.: HY-P1206
CAS. Nr.: 174688-78-9
Target:  

Somatostatin Receptor

Forschungsgebiete:  

Neurological Disease

CH 275 is a peptidic somatostatin analog that acts as an agonist of SST1 (IC50 = 30.9 nM, Ki = 52 nM). The IC50 values of CH 275 for sst3, sst4, sst2, and sst5 are 345 nM, >1 μM, >10 μM, and >10 μM, respectively. CH 275 binds to SSTR1 via the IAmp9-Asp137 ion pair interaction and the hydrophobic interaction between the isopropyl group of IAmp9 and Leu107, and reduces the extracellular acidification rate. CH 275 induces weak sst1 internalization, exerts immunosuppressive effects on macrophages, and decreases macrophage viability, MCP-1 expression/secretion, and IL-8 secretion, but does not alter proMMP-9 secretion or IL-8 mRNA levels. CH 275 reduces hippocampal β-amyloid levels and alleviates plaque pathology without inducing hippocampal microglial activation. CH 275 is used in research on Alzheimer's disease, Parkinson's disease, and depression .
loading...
    loading...
1
1 Cited Publications
Art. -Nr.: HY-107426
CAS. Nr.: 3148-09-2
Reinheit:  99.89%
Synonyms: Muconomycin A
Forschungsgebiete:  

Cancer

Verrucarin A (Muconomycin A), a Type D macrocyclic mycotoxin derived from the pathogen fungus Myrothecium verrucaria, is an inhibitor of protein synthesis. Verrucarin A inhibits growth of leukemia cell lines and activates caspases and apoptosis and inflammatory signaling in macrophages. Verrucarin A effectively increased the phosphorylation of p38 MAPK and diminished the phosphorylation of ERK/Akt. Verrucarin A caused cell cycle deregulation through the induction of p21 and p53 .
loading...
    loading...
1
1 Cited Publications
Art. -Nr.: HY-13756S
CAS. Nr.: 1356841-89-8
Reinheit:  98.36%
Synonyms: FK506-13C,d2; Fujimycin-13C,d2; FR900506-13C,d2
Tacrolimus- 13C,d2 (FK506- 13C,d2) is the 13C, deuterated-labeled Tacrolimus (HY-13756). Tacrolimus (FK506), a molecular glue, a macrocyclic lactone, binds to FK506 binding protein (FKBP) to form a complex. Tacrolimus inhibits calcineurin phosphatase, which inhibits T-lymphocyte signal transduction and IL-2 transcription. Immunosuppressive properties .
loading...
    loading...
Art. -Nr.: HY-P3502
CAS. Nr.: 1841136-73-9
Synonyms: RA101495; RA3193
Target:  

Complement System

Forschungsgebiete:  

Inflammation/Immunology

Zilucoplan (RA101495), a 15-amino acid macrocyclic peptide, is a potent complement component 5 (C5) inhibitor. Zilucoplan can be used in research of immune-mediated necrotising myopathy (IMNM) .
loading...
    loading...
Art. -Nr.: HY-N7765
CAS. Nr.: 104987-36-2
Oenothein B is a dimeric macrocyclic ellagitannin and has widely pharmacological activities, including antioxidant, anti-inflammatory, antifungal, anti-HCV, and antitumor properties. Oenothein B is a potent and specific inhibitor of poly(ADP-ribose) glycohydrolase .
loading...
    loading...
Art. -Nr.: HY-W007656
CAS. Nr.: 294-90-6
Cyclen is a macrocyclic tetraamine chelating agent. Cyclen is the aza analogue of crown ether, used as a precursor for MRI contrast agents, and is an intermediate for the preparation of effective macrocyclic chelates. Cyclen is employed as a structural regulator through interfacial polymerization of polyethleneimine (PEI) and trimesoyl chloride (TMC) to develop polyamide NF membrane with efficient Li +/Mg 2+ separation performance. Cyclen has specific cavity structure and exhibits selective coordination properties for Li + ions [1][2].
loading...
    loading...
Art. -Nr.: HY-P10033
CAS. Nr.: 245080-24-4
Target:  

Ser/Thr Protease

Forschungsgebiete:  

Others

SFTI-1 is a cyclic peptide trypsin inhibitor consisting of 14 amino acid residues. SFTI-1 belongs to the Bowman-Birk class of inhibitors. Characterized by its small size, high stability, and potent activity, SFTI-1 can be used for research on peptide drug design platforms .
loading...
    loading...