81 Results for "

PSI

" in MedChemExpress (MCE) Product Catalog:
Products (81)

81 Results for "PSI" in MCE Product Catalog:

Cat. No.: HY-I0516
CAS No.: 1233335-78-8
Synonyms: GS-566500
Target:  

Endogenous Metabolite

Research Areas:  

Infection

PSI 352707 (GS-566500) is a sofosbuvir metabolite with activity similar to other antiviral compounds. PSI 352707 showed good safety and tolerability in inhibiting chronic hepatitis C virus infection .
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Cat. No.: HY-14308
CAS No.: 1064684-44-1
Synonyms: PSI-7851
Target:  

Endogenous Metabolite

Research Areas:  

Infection

GS-9851 (PSI-7851) is a HCV nonstructural protein 5B (NS5B) inhibitor with potential activity for the study of HCV infection. GS-9851 shows good tolerability with initial HCV genotype 1 infection. GS-9851 is rapidly cleared from the body with a half-life of approximately 1 hour .
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Cat. No.: HY-P2385
CAS No.: 186023-49-4
Research Areas:  

Others

Fmoc-Val-Ser(psi(Me,Me)pro)-OH is a dipeptide.
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Cat. No.: HY-P2393
CAS No.: 168216-05-5
Research Areas:  

Others

Fmoc-Val-Thr(psi(Me,Me)pro)-OH is a dipeptide.
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Cat. No.: HY-P2396
CAS No.: 957780-52-8
Research Areas:  

Others

Fmoc-Ile-Thr(psi(Me,Me)pro)-OH is a dipeptide.
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Cat. No.: HY-P2400
CAS No.: 955048-89-2
Research Areas:  

Others

Fmoc-Leu-Thr(psi(Me,Me)pro)-OH is a dipeptide.
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Cat. No.: HY-P2409
CAS No.: 1196703-48-6
Research Areas:  

Others

Fmoc-Phe-Thr(psi(Me,Me)pro)-OH is a dipeptide.
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Cat. No.: HY-P1258A
Synonyms: Proteasome Inhibitor 1 TFA; Z-Ile-Glu(OtBu)-Ala-Leu-CHO TFA
Target:  

Proteasome

Research Areas:  

Infection Cancer

PSI (TFA) is a potent proteasome inhibitor. PSI (TFA) inhibits the proliferation of primary effusion lymphoma (PEL) cells. PSI (TFA) can be used for the research of Kaposi’s sarcoma-associated herpesvirus (KSHV) infection and KSHV-associated lymphomas .
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Cat. No.: HY-P2404
CAS No.: 920519-32-0
Research Areas:  

Others

Fmoc-Asp(OtBu)-Thr(psi(Me,Me)pro)-OH is a dipeptide.
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Cat. No.: HY-P2408
CAS No.: 936707-21-0
Research Areas:  

Others

Fmoc-Trp(Boc)-Thr(psi(Me,Me)pro)-OH is a dipeptide.
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Cat. No.: HY-P2384
CAS No.: 909115-33-9
Research Areas:  

Others

Fmoc-Glu(OtBu)-Ser(psi(Me,Me)pro)-OH is a dipeptide.
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Cat. No.: HY-P2397
CAS No.: 957780-59-5
Research Areas:  

Others

Fmoc-Asn(Trt)-Thr(psi(Me,Me)pro)-OH is a dipeptide.
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Cat. No.: HY-P2401
CAS No.: 920519-33-1
Research Areas:  

Others

Fmoc-Asn(Trt)-Ser(psi(Me,Me)pro)-OH is a dipeptide.
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Cat. No.: HY-P2403
CAS No.: 955048-92-7
Research Areas:  

Others

Fmoc-Asp(OtBu)-Ser(psi(Me,Me)pro)-OH is a dipeptide.
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Cat. No.: HY-P2412
CAS No.: 908601-15-0
Research Areas:  

Others

Fmoc-Trp(Boc)-Ser(psi(Me,Me)pro)-OH is a dipeptide.
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Cat. No.: HY-103292
CAS No.: 118122-39-7
Target:  

Bradykinin Receptor

Research Areas:  

Cardiovascular Disease

[Phe8Ψ(CH-NH)Arg9]-Bradykinin is a selective Bradykinin receptor B2 agonist (not cleaved by protein kinase I/II). [Phe8Ψ(CH-NH)Arg9]-Bradykinin has potential for the research of hypertension .
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Cat. No.: HY-P2394
CAS No.: 1266350-99-5
Research Areas:  

Others

Fmoc-Ser(tBu)-Thr(psi(Me,Me)pro)-OH is a dipeptide .
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Cat. No.: HY-P2411
CAS No.: 1572725-72-4
Research Areas:  

Others

Fmoc-Gln(Trt)-Thr(psi(Me,Me)pro)-OH is a pseudoproline dipeptide that can be used in Fmoc solid-phase peptide synthesis.
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Cat. No.: HY-W130844
CAS No.: 1676104-73-6
Research Areas:  

Others

Fmoc-Thr(tBu)-Thr(Psi(Me, Me)Pro)-OH is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
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Cat. No.: HY-138232
CAS No.: 141365-20-0
Synonyms: LTNAM
Target:  

Aminopeptidase

Research Areas:  

Neurological Disease

Lys-psi(CH2NH)-Trp(Nps)-OMe is a lysine-tryptophan (Nps) pseudodipeptide analog. It is obtained by replacing the peptide bond in the Lys-Trp(Nps) molecule with an aminomethylene bond and has analgesic activity. Lys-psi(CH2NH)-Trp(Nps)-OMe induces a dose-dependent and naloxone-reversible analgesia after intracerebroventricular administration in mice, and its analgesic effect lasts longer than that of the original compound. It protects methionine enkephalin from degradation in rat striatal slices and binds to low-dose opioid peptides to produce analgesia. Lys-psi(CH2NH)-Trp(Nps)-OMe effectively inhibits brain aminopeptidase activity both in vitro and in vivo. The enhanced resistance of this pseudodipeptide to proteolysis may explain its prolonged analgesic activity.
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