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Cat No. | Product Name | Synonyms | Targets |
---|---|---|---|
T17946 | Fmoc-Ala-Ala-Asn(Trt)-OH | Others | |
Fmoc-Ala-Ala-Asn(Trt)-OH is a cleavable linker vital in ADC synthesis. Fmoc-Ala-Ala-Asn(Trt)-OH joins cytotoxic drugs to antibodies, enabling precise delivery to cells or proteins. The cleavable nature ensures controlled... | |||
T14331 | Gusacitinib | ASN-002 | JAK , Syk |
Gusacitinib (ASN-002) (ASN-002) is spleen tyrosine kinase (SYK) and janus kinase (JAK) inhibitor (IC50: 5-46 nM). | |||
TP2305 | PGlu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val | Others | |
pGlu-Gln-Arg-Leu-Gly-Asn-Gln-Trp-Ala-Val is a peptides | |||
TP2506 | Ser-Asn-Thr-Arg | ||
Ser-Asn-Thr-Arg is a tetrapeptide compound formed by truncation of a transcription activator-like effector. | |||
T38984 | Z-Ala-Ala-Asn-AMC | Cbz-Ala-Ala-Asn-AMC,Z-Ala-Ala-Asn-AMC | |
Z-Ala-Ala-Asn-AMC, also known as Cbz-Ala-Ala-Asn-AMC, serves as a substrate for legumain. The overexpression of legumain in 293 HEK-Leg cells results in efficient cleavage of Cbz-Ala-Ala-Asn-AMC. | |||
T30161 | EN3356 | AS N001,ASN-001 | P450 |
EN3356 is an orally available and selective inhibitor of steroidal 17-alpha-hydroxylase/C17,20 cleavage enzyme (CYP17A1 or CYP17), a non-steroidal cleavage enzyme-selective compound with potential anti-androgenic and ant... | |||
T38116 | Fmoc-Ala-Glu-Asn-Lys-NH2 | Fmoc-Ala-Glu-Asn-Lys-NH2 | |
Fmoc-Ala-Glu-Asn-Lys-NH2 is a peptide inhibitor that selectively targets asparagine endopeptidase (AEP) and inhibits the cleavage of amyloid precursor protein (APP). AEP, a pH-controlled cysteine proteinase, plays a cruc... | |||
T40139 | H-Asn-Arg-OH | ||
H-Asn-Arg-OH is used for the solid-phase peptide synthesis. | |||
TN3748 | D-Asparagine | H-D-Asn-OH | Others , Endogenous Metabolite |
D-Asparagine (H-D-Asn-OH) is a source of nitrogen for yeast strains. D-Asparagine is a competitive inhibitor of L-Asparagine hydrolysis (Ki = 0.24 mM). | |||
T38713 | Fmoc-L-Asn(beta-D-GlcNAc(Ac)3)-OH | Fmoc-Asn(Ac3AcNH-beta-Glc)-OH,Fmoc-L-Asn(beta-D-GlcNAc(Ac)3)-OH | |
Fmoc-L-Asn(beta-D-GlcNAc(Ac)3)-OH, also known as Fmoc-Asn(Ac3AcNH-beta-Glc)-OH, is a chemical compound used in the synthesis of silicon-fluoride acceptor (SiFA) derivatized octreotate derivatives. SiFA-octreotate analogu... | |||
T17365 | Ala-Ala-Asn-PAB | Others | |
Ala-Ala-Asn-PAB is a peptide cleavable ADC linker for antibody-drug conjugates (ADCs)[1]. | |||
T14455 | Azido-PEG5-Ala-Ala-Asn-PAB | Others | |
Azido-PEG5-Ala-Ala-Asn-PAB is a cleavable 5-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T2O2774 | L-Asparagine | alpha-aminosuccinamic acid,(-)-Asparagine,Asparamide,2-Aminosuccinamic acid,Asn,Altheine | Endogenous Metabolite |
L-Asparagine (Asparamide) is a non-essential amino acid that is involved in the metabolic control of cell functions in nerve and brain tissue. It is biosynthesized from ASPARTIC ACID and AMMONIA by asparagine synthetase. | |||
T15331 | Fmoc-PEG4-Ala-Ala-Asn-PAB | Others | |
Fmoc-PEG4-Ala-Ala-Asn-PAB is a four-unit polyethylene glycol (PEG) linker, cleavable in nature. It is specifically employed for the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T17945 | Fmoc-Ala-Ala-Asn-PABC-PNP | Others | |
Fmoc-Ala-Ala-Asn-PABC-PNP is a peptide cleavable ADC linker[1]. | |||
T8865 | ASN03576800 | Others | |
ASN03576800 is an inhibitor of the VP40 matrix protein. | |||
T15329 | Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB | Others | |
Fmoc-PEG3-Ala-Ala-Asn(Trt)-PAB is a cleavable three-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1]. | |||
T82957 | ASN 07115873 | ||
ASN 07115873 is an anti-Zika virus (ZIKV) compound with an inhibitory concentration (IC50) of 189.2 picomolar (pM), suitable for antiviral research [1]. | |||
T41067 | Fmoc-Asn(Trt)-Ser(psi(Me,Me)pro)-OH | ||
Fmoc-Asn(Trt)-Ser(psi(Me,Me)pro)-OH is a dipeptide. | |||
T30274 | Azido-PEG4-Ala-Ala-Asn(Trt)-PAB | ||
Azido-PEG4-Ala-Ala-Asn(Trt)-PAB is a PEG derivative conjugated with a peptide via an amide bond. The azide group on the PEG end enables Click Chemistry. The hydrophilic PEG spacer increases solubility in aqueous media. |