219 Results for "

Cyclohexanemethanol-d11

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

219 Results for "Cyclohexanemethanol-d11" in MCE Product Catalog:

Cat. No.: HY-125745
CAS No.: 182422-45-3
Target:  

Antibiotic Bacterial

Research Areas:  

Infection

Loloatin B 10 is an antibiotic, which exhibits antibacterial efficacy against gram positive antibiotic resistant human pathogens .
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Cat. No.: HY-P11911
Cyclo(Val-Val-Ile-d-Ala-Trp(7-Br)-Gly) is a cyclic peptide containing 7-bromotryptophan, designed as a precursor for Sonogashira cross-coupling to generate a BODIPY-conjugated probe selective for prefibrillar 1−42 oligomers .
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Cat. No.: HY-P2436
CAS No.: 125989-10-8
Target:  

Neurokinin Receptor

Research Areas:  

Neurological Disease

L-659837 is a NK2 receptor antagonist, and can antagonize GR 64349 (HY-P1278)-induced contraction. L-659837 can be used for study of urinary bladder disorders .
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Cat. No.: HY-P3228
CAS No.: 153982-38-8
Target:  

Endothelin Receptor

Research Areas:  

Cardiovascular Disease

JKC 302 is an ET-A receptor antagonist. JKC 302 partly blocks ET-1-induced contraction in asthmatic rat trachea ring .
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Cat. No.: HY-P4201
CAS No.: 136553-96-3
Target:  

Vasopressin Receptor

Research Areas:  

Cardiovascular Disease

JKC 301 is a selective Endothelin A receptor antagonist. JKC 301 attenuates the pressor effects of nicotine in rats. JKC 301 can be used to study cardiovascular disease caused by smoking .
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Cat. No.: HY-120301
CAS No.: 127819-96-9
Target:  

Oxytocin Receptor

Research Areas:  

Endocrinology

L-366682, a cyclic hexapeptide, possesses antagonism of oxytocin .
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Cat. No.: HY-P10714
CAS No.: 2396736-46-0
Research Areas:  

Cancer

Ub4ix is a DUB/26S proteasome inhibitor. Ub4ix can protect K48-linked Ub chains from being chopped up by deubiquitinating enzymes (DUBs) and prevent the proteasomal degradation of Ub-tagged proteins. Ub4ix can reduce the viability of Hela cells and induce apoptosis, with an IC50 value of 1.6 μM .
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Cat. No.: HY-P10860
CAS No.: 2853605-24-8
Target:  

Factor Xa

Research Areas:  

Cardiovascular Disease

cMCoFx1 is a potent and selective FXIIa cyclic peptide inhibitor. cMCoFx1 has high binding affinity (KD: 900 pM) and inhibitory activity (Ki: 370 pM) for FXIIa. cMCoFx1 can effectively inhibit endogenous clotting pathways, and cMCoFx1 is stable in serum and non-cytotoxic .
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Cat. No.: HY-P11856
Research Areas:  

Cancer

cPP12-2-Lys is a cyclic cell-penetrating peptide that serves as a negative control, i.e., it lacks any NatD bisubstrate moiety. cPP12-2-Lys is not a NatD inhibitor (IC50 = 9500 nM), but it possesses excellent cell-penetrating ability and can mediate the entry of conjugated bisubstrate inhibitors into non-small cell lung cancer (NSCLC) cells. cPP12-2-Lys can be used in NSCLC research .
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Cat. No.: HY-P3293
CAS No.: 906547-89-5
Synonyms: POL6014
Target:  

Elastase

Research Areas:  

Inflammation/Immunology

Lonodelestat (POL6014) is a potent, orally active and selective peptide inhibitor of human neutrophil elastase (hNE). Lonodelestat (POL6014) has the potential for the research of cystic fibrosis (CF) .
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Cat. No.: HY-P0036A
CAS No.: 1607842-55-6
Synonyms: SMS 201-995 dihydrochloride
Octreotide (SMS 201-995) hydrochloride is a somatostatin receptor agonist and synthetic octapeptide endogenous somatostatin analogue. Octreotide hydrochloride can bind to the somatostatin receptors which are mainly subtypes 2, 3 and 5. Octreotide hydrochloride increases Gi activity and reduces intracellular cAMP production. Octreotide hydrochloride has antitumor activity, mediates apoptosis and may also be used in disease studies in acromegaly .
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Cat. No.: HY-P4910
CAS No.: 1622872-91-6
Target:  

Proteasome Apoptosis

Research Areas:  

Cancer

Baceridin is a proteasome inhibitor and a cyclic hexapeptide. Baceridin can be isolated from the culture medium of Epiphytic Bacillus. Baceridin can inhibit cell cycle progression and induce tumor cell apoptosis through a p53-independent pathway. Baceridin can be used in cancer research .
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Cat. No.: HY-P5098
CAS No.: 250612-47-6
Target:  

Integrin

Research Areas:  

Neurological Disease Cancer

E (c (RGDfK)) 2 is a αvβ3 integrin ligand and tumor-targeting agent. E (c (RGDfK)) 2 binds to αvβ3 integrin, mediates receptor-mediated endocytosis of conjugated payloads, and inhibits integrin-dependent cell adhesion to fibrinogen. E (c (RGDfK)) 2 inhibits the proliferation of cancer cells and endothelial cells. E (c (RGDfK)) 2 preferentially accumulates in orthotopic mouse breast tumors and human ovarian cancer xenograft tumors. E (c (RGDfK)) 2 can be used in research related to glioblastoma, lung cancer, breast adenocarcinoma and ovarian cancer .
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Cat. No.: HY-P10051
CAS No.: 1782098-79-6
Target:  

Ras Raf

Research Areas:  

Cancer

Cyclorasin 9A5 is an 11-residue cell-permeable cyclic peptide that orthosterically inhibits the Ras-Raf protein interaction with an IC50 of 120 nM .
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Cat. No.: HY-P10051A
Target:  

Ras Raf

Research Areas:  

Cancer

Cyclorasin 9A5 TFA is an 11-residue cell-permeable cyclic peptide that orthosterically inhibits the Ras-Raf protein interaction with an IC50 of 120 nM .
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Cat. No.: HY-P10203
Target:  

Opioid Receptor

Research Areas:  

Inflammation/Immunology

μ/κ/δ opioid receptor agonist 1 is a μ opioid receptor (MOR), κ opioid receptor (KOR), and δ opioid receptor (DOR) agonist. μ/κ/δ opioid receptor agonist 1 produces a strong and long-lasting analgesic effect through peripheral MOR and KOR in the tail-flick test .
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Cat. No.: HY-P10588
CAS No.: 151928-32-4
Target:  

Neurokinin Receptor

Research Areas:  

Others

WIN 66306 is a cyclic heptapeptide that can be isolated from an Aspergillus species. WIN 66306 is a neurokinin antagonist with antagonistic effects on both NK1 and NK2 receptors .
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Cat. No.: HY-P10644
CAS No.: 1831064-63-1
Target:  

Fluorescent Dye

Research Areas:  

Cancer

CPP9 is a small, amphipathic, cyclic cell penetrating peptide (CPP). CPPs bind directly to the plasma membrane phospholipids and enter mammalian cells via endocytosis, followed by efficient release from the endosome. CPP9 can be used for intracellular delivery of therapeutic agents and chemical probes .
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Cat. No.: HY-P10644A
Target:  

Inhibitory Antibodies

Research Areas:  

Cancer

CPP9 TFA is a small, amphipathic, cyclic cell penetrating peptide (CPP). CPPs bind directly to the plasma membrane phospholipids and enter mammalian cells via endocytosis, followed by efficient release from the endosome. CPP9 TFA can be used for intracellular delivery of therapeutic agents and chemical probes .
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Cat. No.: HY-P11824
Research Areas:  

Cancer

CoA-C2-SGRGK-cCPP is a NatD (NAA40) bisubstrate inhibitor with an IC50 of 78 nM and a Ki of 39 nM. CoA-C2-SGRGK-cCPP competitively targets the peptide substrate binding site and noncompetitively targets the CoA binding site of NatD to block acetyltransferase activity. CoA-C2-SGRGK-cCPP reduces cellular Nα-acetylation on histone H4, modulates EMT marker expression. CoA-C2-SGRGK-cCPP can be used for the research of non-small cell lung cancer .
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