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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC41941 | Fmoc-Gln(Trt)-Ser(psi(Me,Me)pro)-OH |
Fmoc-Gln(Trt)-Ser(psi(Me,Me)pro)-OH is a dipeptide.
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| DC41940 | Fmoc-Leu-Ser(psi(Me,Me)pro)-OH |
Fmoc-Leu-Ser(psi(Me,Me)pro)-OH is a dipeptide.
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| DC41939 | Fmoc-Lys(Boc)-Ser(psi(Me,Me)pro)-OH |
Fmoc-Lys(Boc)-Ser(psi(Me,Me)pro)-OH is a dipeptide.
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| DC41938 | Fmoc-Lys(Boc)-Thr(psi(Me,Me)pro)-OH |
Fmoc-Lys(Boc)-Thr(psi(Me,Me)pro)-OH is a dipeptide.
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| DC41937 | Fmoc-Tyr(tBu)-Ser(psi(Me,Me)pro)-OH |
Fmoc-Tyr(tBu)-Ser(psi(Me,Me)pro)-OH is a dipeptide.
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| DC41936 | Fmoc-Ala-Ser(psi(Me,Me)pro)-OH |
Fmoc-Ala-Ser(psi(Me,Me)pro)-OH is a dipeptide.
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| DC41935 | Fmoc-Val-Ser(psi(Me,Me)pro)-OH |
Fmoc-Val-Ser(psi(Me,Me)pro)-OH is a dipeptide.
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| DC41934 | Fmoc-Glu(OtBu)-Ser(psi(Me,Me)pro)-OH |
Fmoc-Glu(OtBu)-Ser(psi(Me,Me)pro)-OH is a dipeptide.
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| DC41933 | TRV120056 |
TRV120056 is a Gq-biased agonists, exhibits 10-fold larger molecular efficacies at the AT1R-Gq fusion protein compared with the AT1R-βarr2 fusion protein.
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| DC41932 | TRV120055 |
TRV120055 is a Gq-biased agonists, exhibits 10-fold larger molecular efficacies at the AT1R-Gq fusion protein compared with the AT1R-βarr2 fusion protein.
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| DC41931 | S12 TFA |
G12 (Ras 5-17) is a wild-type Ras peptide consisted of amino acids 5-17 (KLVVVGAGGVGKS). G12 can be used as a control of mutant Ras peptides studies (such V12).
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| DC41930 | S12 |
S12 is a mutant RAS peptide containing the Gly (G) to Ser (S12) substitution. The sequence of the peptide is KLVVVGASGVGKS.
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| DC41929 | G12 TFA |
G12 (Ras 5-17) TFA is a wild-type Ras peptide consisted of amino acids 5-17 (KLVVVGAGGVGKS). G12 TFA can be used as a control of mutant Ras peptides studies (such V12).
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| DC41928 | G12 |
G12 (Ras 5-17) is a wild-type Ras peptide consisted of amino acids 5-17 (KLVVVGAGGVGKS). G12 can be used as a control of mutant Ras peptides studies (such V12).
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| DC41927 | PSMα3 |
PSMα3 is a peptide for manipulating DCs to become tolerogenic for DC vaccination strategies. PSMα3 penetrates and modulates human monocyte-derived DCs by altering the TLR2- or TLR4-induced maturation, inhibiting pro- and anti-inflammatory cytokine production and reducing antigen uptake. PSMα3 is an important toxin released by the most virulent strains of methicillin-resistant Staphylococcus aureus (MRSA).
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| DC41926 | {Boc}-Phe-Leu-Phe-Leu-Phe TFA |
{Boc}-Phe-Leu-Phe-Leu-Phe TFA is a formyl peptide receptor (FPR) family antagonist that preferentially inhibits activity triggered through the formyl peptide receptor.
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| DC41925 | {Boc}-Phe-Leu-Phe-Leu-Phe |
{Boc}-Phe-Leu-Phe-Leu-Phe ({Boc}-FLFLF) is a formyl peptide receptor (FPR) family antagonist that preferentially inhibits activity triggered through the formyl peptide receptor.
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| DC41924 | Fetuin, Fetal Bovine Serum |
Fetuin, Fetal Bovine Serum is a liver-secreted 64 kDa plasma glycoprotein isolated from fetal bovine serum. Fetuin, Fetal Bovine Serum inhibits trypsin activity and promote cellular attachment, growth, and differentiation.
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| DC41920 | Angiopep-Bim BH3 hydrochloride |
Angiopep-Bim BH3 hydrochloride, a BBB penetrated peptode, could be used to investigate the permeability of CNS therapeutics.
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| DC41919 | Angiopep-2 hydrochloride |
Angiopep-2 hydrochloride is a brain peptide vector. The conjugation of anticancer agents with the Angiopep-2 peptide vector could increase their efficacy in the treatment of brain cancer.
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| DC41918 | LCKLSL hydrochloride |
LCKLSL hydrochloride is a N-terminal hexapeptide and a competitive annexin A2 (AnxA2) inhibitor. LCKLSL hydrochloride potently inhibits the binding of tissue plasminogen activator (tPA) to AnxA2. LCKLSL hydrochloride also inhibits the generation of plasmin and has anti-angiogenic roles.
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| DC41917 | LCKLSL |
LCKLSL is a N-terminal hexapeptide and a competitive annexin A2 (AnxA2) inhibitor. LCKLSL potently inhibits the binding of tissue plasminogen activator (tPA) to AnxA2. LCKLSL also inhibits the generation of plasmin and has anti-angiogenic roles.
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| DC41898 | TAT-P4-(DATC5)2 TFA |
TAT-P4-(DATC5)2 TFA is a high-affinity peptide inhibitor of the PICK1 (protein interacting with C kinase-1) PDZ domain, with a Ki of 1.7 nM. TAT-P4-(DATC5)2 TFA attenuats the reinstatement of cocaine seeking in rats.
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| DC41897 | TAT-P4-(DATC5)2 |
TAT-P4-(DATC5)2 is a high-affinity peptide inhibitor of the PICK1 (protein interacting with C kinase-1) PDZ domain, with a Ki of 1.7 nM. TAT-P4-(DATC5)2 attenuats the reinstatement of cocaine seeking in rats.
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| DC41896 | TfR-T12 TFA |
TfR-T12 TFA is a BBB-penetrated transferrin receptor (TfR) binding peptide, displaying a binding affinity in the nM range.
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| DC41894 | Dabcyl-KTSAVLQSGFRKME-Edans TFA |
Dabcyl-KTSAVLQSGFRKME-Edans TFA is a fluorogenic peptide. Dabcyl-KTSAVLQSGFRKME-Edans TFA is used as the substrate to measure the enzymatic activities of protease forms. Dabcyl-KTSAVLQSGFRKME-Edans TFA has the potential for study 2019-nCoV (COVID-19) infection.
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| DC41886 | AC 253 |
AC 253 is an Amylin (AMY3) receptor antagonist, inhibiting andrenomedulin-stimulated cAMP production. AC 253 protects against oligomeric Aβ-induced increase in intracellular Ca2+, activation of PKA, MAPK, Akt and cFOS and cell death in neuronal cell culture. AC 253 blocks electrophysiological effects of Aβ.
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| DC41885 | Amyloid β-Peptide (1-37) (human) |
Amyloid β-Peptide (1-37) (human) is an amyloid β-protein fragment cleaved from amyloid precursor protein (APP).
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| DC41879 | Histone H3 (1-34) |
Histone H3 (1-34), a peptide derived from human histone isotype 3.1, is a substrate for methyltransferase/demethylase enzymes.
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| DC41878 | H3K4(Me3) (1-20) |
H3K4(Me3) (1-20), a histone peptide, is a substrate for methyltransferase/demethylase enzymes.
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