231 Results for "

2-(2-Chlorophenyl)-2-hydroxycyclohexanone

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

231 Results for "2-(2-Chlorophenyl)-2-hydroxycyclohexanone" in MCE Product Catalog:

Cat. No.: HY-P11912
Research Areas:  

Neurological Disease

Cyclo (Val-Val-Ile-d-Ala-Trp (Bodipy)-Gly) is a cyclic peptide-BODIPY conjugate. Cyclo (Val-Val-Ile-d-Ala-Trp (Bodipy)-Gly) detects prefibrillar 1-42 aggregates in neuronal cells, generating perinuclear punctate fluorescent spots. Cyclo (Val-Val-Ile-d-Ala-Trp (Bodipy)-Gly) is applicable to Alzheimer's disease-related research .
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Cat. No.: HY-P4755
CAS No.: 282726-24-3
Research Areas:  

Others

N-((RS)-2-Hydroxy-propyl)-Val-Leu-anilide is a polypeptide composed of L-phenyleline and L-leucine bound to aniline groups. N-((RS)-2-Hydroxy-propyl)-Val-Leu-anilide can be used to quantitatively determine the N-terminal heme adduct formed upon exposure to propylene oxide (PO) .
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Cat. No.: HY-P4992
CAS No.: 496849-46-8
Target:  

Somatostatin Receptor

Research Areas:  

Cancer

Tyr-(D-Dab4,Arg5,D-Trp8)-cyclo-Somatostatin-14 (4-11) is a somatostatin agonist that can be used in cancer research .
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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-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-P4948
CAS No.: 1926163-49-6
Research Areas:  

Others

Coumarin-phalloidin is a kind of phalloidin labeled with Coumarin (HY-N0709). Coumarin-phalloidin is a new type of actin probe that can be used for triple immunofluorescence microscopic observation of the cell skeleton .
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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-158104
Target:  

ATF6

Research Areas:  

Others

LPPM-8 is a ligand of Med25 and an inhibitor of Med25 protein-protein interactions (PPIs). LPPM-8 engages Med25 through interaction with the H2 face of its Activator Interaction Domain and stabilizes full-length protein in the cellular proteome. LPPM-8 is an orthosteric inhibitor of H2-binding transcriptional activators (such as ATF6a). LPPM-8 can be used for studying Med25 and Mediator complex biology .
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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-P3100
CAS No.: 939960-34-6
Target:  

Parasite

Research Areas:  

Infection

Orfamide A is a major metabolite of insecticidal biosurfactant in Pseudomonas sp. F6 and has aphidicidal activity. Orfamide A can be used for aphid control in organic agriculture. Orfamide A exhibits dose-dependent mortality against aphids with an LC50 value of 34.5 μg/mL .
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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-125357
CAS No.: 148619-41-4
Target:  

Inhibitory Antibodies

Research Areas:  

Metabolic Disease

Ternatin (compound 2) is a cyclic heptapeptides that can be isolated from mushroom Coliorus versicolor. Ternatin inhibits fat-accumulation with an IC50 of 0.027 μM in 3T3-L1 adipocytes .
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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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