231 Results for "

2,2,6-Trimethylcyclohexanone

" in MedChemExpress (MCE) Product Catalog:
Products (231)

231 Results for "2,2,6-Trimethylcyclohexanone" in MCE Product Catalog:

Cat. No.: HY-P5738
CAS No.: 331714-57-9
Target:  

Bacterial

Research Areas:  

Infection

Palicourein is a 37 amino acid cyclic polypeptide. Palicourein inhibits the in vitro cytopathic effects of HIV-1RF infection of CEM-SS cells with an EC50 value of 0.1 μM and an IC50 value of 1.5 μM .
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Cat. No.: HY-P5739
CAS No.: 1803183-45-0
Target:  

Bacterial

Research Areas:  

Infection

Mram 8 is a cyclotide isolated from Viola philippica, a plant from the Violaceae family .
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Cat. No.: HY-P5753
CAS No.: 1873323-60-4
Target:  

Bacterial

Research Areas:  

Infection

JB-95, a β-hairpin macrocyclic peptide, exhibits potent antimicrobial activity against Escherichia coli. JB-95 can selectively disrupt the outer membrane but not the inner membrane of E. coli .
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Cat. No.: HY-P5753A
Target:  

Bacterial

Research Areas:  

Infection

JB-95 acetate, a β-hairpin macrocyclic peptide, exhibits potent antimicrobial activity against Escherichia coli. JB-95 acetate can selectively disrupt the outer membrane but not the inner membrane of E. coli .
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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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