fmoc-n-me-val-oh

Fmoc-N-Me-Val-OH is a modified peptide.

Fmoc-D-N-Me-Val-OH is a useful organic compound for research related to life sciences. The catalog number is T65652 and the CAS number is 103478-58-6.

Fmoc-Val-Cit-PAB is a linker for antibody-drug-conjugation (ADC).

Val-cit-PAB-OH is an ADC linker that is cleavable.

FMOC-NIP-OH is a piperidinecarboxylic acid derivative.

N-Me-aminopyrimidinone9 is a sodium channel antagonist

Mal-PEG1-Val-Cit-OH is a cleavable one-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].

Fmoc-Gly-Ser(psi(Me,Me)pro)-OH acetate is a dipeptide.

Fmoc-N-methyl-L-alloisoleucine is a biochemical reagent for biosynthesis.

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 drug release, optimizing ADC effectiveness.

Fmoc-N-Me-Leu-OH is available for the peptide-coupling reaction.

DBCO-Val-Cit-PABC-OH is a cleavable linker employed in the synthesis of antibody-drug conjugates (ADCs) [1].

Mal-PEG2-Val-Cit-amido-PAB-OH is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

Fmoc-Gly-Thr(psi(Me,Me)pro)-OH is a polypeptide composed of two amino acids.

Fmoc-Thr(GalNAc(Ac)3-β-D)-OH impedes the proliferation of cancer cells by selectively interacting with complex oncogenic pathways and enhancing the immune response [1].

N-Me-N-bis(PEG4-acid) is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

N-Me-N-bis-PEG4 is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Fmoc-Lys-OH hydrochloride is a alkyl-chain-based PROTAC linker. Fmoc-Lys-OH hydrochloride is a non-cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).

Fmoc-Val-D-Cit-PAB is a cleavable linker for antibody-drug-conjugation (ADC).

Fmoc-N-PEG24-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.

Fmoc-Tyr(3-F, tBu)-OH is a cyclic peptide compound possessing high membrane permeability and exhibiting specific binding affinity towards a target molecule.

SNNF(N-Me)GA(N-Me)ILSS is a biologically active peptide comprising double N-methylated derivatives of an amyloidogenic and cytotoxic partial IAPP sequence.

F(N-Me)GA(N-Me)IL is a bioactive peptide whose double N-methylated derivatives of the partial IAPP sequence lack β-sheet structure, amyloidogenicity, and cytotoxicity. These derivatives can interact with the native sequences to inhibit amyloid formation.

SNNF(N-Me)GA(N-Me)IL is a biologically active peptide comprising double N-methylated derivatives of a partial IAPP sequence known to be amyloidogenic and cytotoxic.

Fmoc-N-Me-Ala-OH is available for the peptide-coupling reaction.

Fmoc-N-Me-Phe-OH (Fmoc-N-methyl-L-phenylalanine) is a Malaria Parasite inhibitor.

Fmoc-Phe(4-CN)-OH is an N-Fmoc protected phenylalanine derivative and potentially useful synthetic intermediate

Fmoc-Val-Cit-PAB-MMAE is consisted of the ADCs linker (Fmoc-Val-Cit-PAB) and potent tubulin inhibitor (MMAE). Fmoc-Val-Cit-PAB-MMAE is a drug-linker conjugate for ADC.

H-Met-Val-OH, a dipeptide with an N-terminal methionine, exhibits inhibition of cDNA-expressed Flavin-containing monooxygenase (FMO) 1 and FMO3, and holds potential for promoting neuritis growth [1] [2].

Val-Cit-amide-Cbz-N(Me)-Maytansine is a molecule that functions both as an antibody and a bispecific antigen-binding entity, targeting the hepatocyte growth factor receptor c-Met (MET), and is used in the formulation of antibody-drug conjugates (ADCs) [1].

H-Val-Thr-Cys-Gly-OH is a cell attachment peptide that functions as a bioactive molecule promoting cell adhesion and facilitating various cell interactions [1].

N-Me-L-Ala-maytansinol used for making antibody-drug conjugate (ADC),is a hydrophobic, cell permeable payload.

FMoc-Arg(Tos)-OH is a synthetic amino acid used in peptide synthesis, biochemistry and molecular biology. It is a Fmoc-protected amino acid used as an intermediate in peptide and protein synthesis for solid-phase peptide synthesis.

Fmoc-Arg-OH (Fmoc-L-Arginine) (Fmoc-L-Arginine) is a used in peptide synthesis.

β-Glucuronide-NB-bis[N(Me)-methyl ester]-MMAE (compound 20), an auristatins-glucuronide conjugate, exhibits in vitro antiproliferative effects on cancer cells, both β-glucuronidase pretreated and untreated, with an IC50 range of 5.7 nM to 9.7 nM. Demonstrating powerful antitumor efficacy in an HCT-116 xenograft mouse model, this compound does not induce side effects [1].

Fmoc-Cys(STmp)-OH is a cysteine derivative that can be used in the synthesis of bicyclic and linear peptides.

NF(N-Me)GA(N-Me)IL is a biologically active peptide, representing a modified segment (amino acids 22 to 27) of the human islet amyloid polypeptide (hIAPP) sequence NFGAIL. This modification includes N-methylations at G24 and I26, transforming the amyloidogenic and cytotoxic nature of the original sequence into a non-amyloidogenic and non-cytotoxic variant. Moreover, the peptide maintains the ability to bind with high affinity to full-length hIAPP, effectively inhibiting its fibril formation.

Fmoc-D-Val-D-Cit-PAB is a cleavable linker for antibody-drug-conjugation (ADC).

Fmoc-D-Val-Cit-PAB is a cleavable linker for antibody-drug-conjugation (ADC).

Boc-Val-Cit-OH is a cleavable ADC linker used in antibody-drug conjugates (ADCs) synthesis.

N6-Benzoyl-7'-OH-N-trityl morpholino adenosine is a Morpholino-nucleoside.

Fmoc-Lys(Pal-Glu-OtBu)-OH is a useful organic compound for research related to life sciences. The catalog number is T66786 and the CAS number is 1491158-62-3.

Fmoc-Tyr(tBu)-Thr(psi(Me,Me)pro)-OH is a useful organic compound for research related to life sciences. The catalog number is T66619 and the CAS number is 920519-31-9.

H-Phe(2-Me)-OH is a useful organic compound for research related to life sciences and the catalog number is T66208.

Fmoc-D-Cha-OH (FDCO) is an apoptotic DNase γ inhibitor that inhibits the release of HMGB1.

Fmoc-Phe(4-NH2)-OH is an amino acid derivative and has a wide range of applications in life science related research.

Fmoc-Gly3-Val-Cit-PAB is a cleavable linker utilized in the assembly of antibody-drug conjugates (ADCs).

OH-Glu-Val-Cit-PAB-MMAE is a compound comprising a cleavable ADC linker (OH-Glu-Val-Cit-PAB) and a potent tubulin inhibitor (MMAE), utilized in the synthesis of antibody-drug conjugates (ADCs) [1].

N,S-Bis-Fmoc-Glutathione is a potent inhibitor of glyoxalase II, exhibiting a K i of 0.32 mM [1].

Fmoc-Lys(Me)3-OH Chloride is a useful organic compound for research related to life sciences. The catalog number is T65200 and the CAS number is 201004-29-7.