219 Results for "

Decyclohexanamine-Exatecan

" in MedChemExpress (MCE) Product Catalog:
Products (219)

219 Results for "Decyclohexanamine-Exatecan" in MCE Product Catalog:

Cat. No.: HY-P5058
CAS No.: 193139-41-2
Target:  

Inhibitory Antibodies

Research Areas:  

Inflammation/Immunology

Cyclolinopeptide B is a cyclic nonapeptide with immunosuppressive activity on human peripheral blood lymphocytes .
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Cat. No.: HY-P5698
CAS No.: 82081-23-0
Cyclopetide 1 (Compound 1) is an antimicrobial peptide with moderate activity against B. subtilis, with a MIC of 25 μg/mL .
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Cat. No.: HY-P5699
CAS No.: 748142-26-9
Cyclopetide 2 (Compound 2) is an antimicrobial peptide with moderate activity against B. subtilis, with a MIC of 50 μg/mL .
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Cat. No.: HY-139741
Target:  

DNA/RNA Synthesis

Research Areas:  

Others

cyclo(Phe-Ala-Gly-Arg-Arg-Arg-Gly-AEEAc) provides an avenue for developing a nonhormonal male contraceptive by blocking of GRTH/DDX25 phosphorylation.
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Cat. No.: HY-P10858
Target:  

SARS-CoV Virus Protease

Research Areas:  

Infection

UCI-1 is a SARS-CoV-2 main protease (M pro) cyclic peptide inhibitor with an IC50 of 160 μM. UCI-1 shows no obvious cytotoxicity at the concentration of inhibiting M pro. UCI-1 can be used in the study of anti-COVID-19 drugs .
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Cat. No.: HY-P4820
Target:  

Bacterial

Research Areas:  

Inflammation/Immunology

SYNV-cyclo(CGGYF) is a Staphylococcus hominis (S. hominis) C5 autoinducing peptide. SYNV-cyclo(CGGYF) inhibits S. aureus activity. SYNV-cyclo(CGGYF) has the potential for the research of S. aureus-mediated epithelial damage and inflammation .
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Cat. No.: HY-P4820A
Target:  

Bacterial

Research Areas:  

Inflammation/Immunology

SYNV-cyclo(CGGYF) TFA is a Staphylococcus hominis (S. hominis) C5 autoinducing peptide. SYNV-cyclo(CGGYF) TFA inhibits S. aureus activity. SYNV-cyclo(CGGYF) TFA has the potential for the research of S. aureus-mediated epithelial damage and inflammation .
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Cat. No.: HY-125488
CAS No.: 226956-07-6
Target:  

Inhibitory Antibodies

Research Areas:  

Others

Unguisin B s a cyclic peptides that can be isolated from the marine-derived fungus Emericella unguis .
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Cat. No.: HY-133801
CAS No.: 226956-06-5
Target:  

Inhibitory Antibodies

Research Areas:  

Others

Unguisin A s a cyclic peptides that can be isolated from the marine-derived fungus Emericella unguis .
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Cat. No.: HY-149205
CAS No.: 2919976-92-2
Target:  

PI3K ERK

Research Areas:  

Inflammation/Immunology

CXJ-2 is a cyclic peptide, and exhibits moderate affinity toward elastin derived peptides (EDPs). CXJ-2 exhibits potent activities to inhibit the PI3K/ERK pathway and decrease hepatic stellate cell proliferation and migration. CXJ-2 possesses potent antifibrotic efficacy .
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Cat. No.: HY-P5032
CAS No.: 75685-88-0
Target:  

Inhibitory Antibodies

Research Areas:  

Others

Cyclo(D-His-Pro) is a polypeptide that can be found by peptide screening. Peptide screening is a research tool that pools active peptides primarily by immunoassay. Peptide screening can be used for protein interaction, functional analysis, epitope screening, especially in the field of agent research and development .
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Cat. No.: HY-P10548
CAS No.: 1221423-80-8
Target:  

Bacterial

Research Areas:  

Infection

Cyclic L27-11 is a peptidomimetic compound targeting the bacterial outer membrane protein LptD. Cyclic L27-11 exhibits nanomolar antibacterial activity against Pseudomonas aeruginosa. Cyclic L27-11 binds to LptD and inhibits the translocation of lipopolysaccharides to the cell surface. Cyclic L27-11 can be used in studies related to Pseudomonas aeruginosa infection .
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Cat. No.: HY-P10845
CAS No.: 2423969-43-9
Target:  

HIV

Research Areas:  

Infection

KRL74 is a cyclic peptide inhibitor for interaction between the p6 domain of the HIV Gag protein and the UEV domain of the human TSG101 protein(p6/UEV) with an IC50 of 5.44 μM and a Kd of 11.9 μM. KRL74 inhibits the budding process of HIV from host cells with an IC50 of 2 μM in virus-like particle (VLP) budding assay .
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Cat. No.: HY-P10855
CAS No.: 3027437-21-1
Target:  

SARS-CoV

Research Areas:  

Infection

S1b3inL1 is a SARS-CoV-2 spike protein macrocyclic peptide inhibitor. S1b3inL1 can bind the conserved site of spike protein with high affinity and inhibit the infection of various SARS-CoV-2 variant strains. S1b3inL1 has antiviral activity .
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Cat. No.: HY-136415
CAS No.: 268221-76-7
Cyclo(Ala-Gln) (Compound 7) is a 2,5-diketopiperazine (DKP, cyclic dipeptide) .
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Cat. No.: HY-N17542
CAS No.: 176392-47-5
Cycloleonuripeptide A is a natural product that can be found in motherwort.
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Cat. No.: HY-N18041
CAS No.: 158335-66-1
Pseudostellarin E is a proline-rich, caryophyllaceous cyclopeptide present in the roots of Pseudostellaria heterophylla. Pseudostellarin E can be synthesized by overexpressing its precursor gene prePhPE in the leaves of Nicotiana benthamiana .
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Cat. No.: HY-P11266
CAS No.: 493012-52-5
Target:  

Inhibitory Antibodies

Research Areas:  

Cancer

Phakellistatin 13 is a natural cycloheptapeptide with anti-tumor activity. Phakellistatin 13 exhibits a potent inhibitory effect on liver cancer cells BEL-7404 (ED500 < 0.01 μg/mL). Phakellistatin 13 can be used for research on liver cancer .
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Cat. No.: HY-P11709
CAS No.: 3106628-26-3
Synonyms: cyclo(CLPVASC)
Target:  

Inhibitory Antibodies

Research Areas:  

Metabolic Disease

CLPVASC is a kidney-targeting cyclic peptide that preferentially distributes to kidney tissue, with utility to enhance kidney targeting of nanocarriers.CLPVASC preferentially distributes to the kidney when displayed on PEG-b-PPS micelles. CLPVASC can be used for the research of acute kidney injury .
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Cat. No.: HY-P11752
Target:  

EGFR

Research Areas:  

Cancer

Cyclo (KLARLLT) is an EGFR ligand with a Kd value of 1.16 μM. Cyclo (KLARLLT) binds to domain I of EGFR and interacts with both the open and closed conformations of EGFR. Cyclo (KLARLLT) is a modified variant of LARLLT (HY-P11078). Cyclo (KLARLLT) can be used in the research of colorectal cancer .
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