TMPD dihydrochloride, a readily oxidizable compound, is an enzymatically convert redox active substrate molecule. TMPD dihydrochloride is also an electron donor and serves as a reducing cosubstrate for heme peroxidases[1][2]. TMPD dihydrochloride is also a complex IV substrate[3].
Guignardone J is the secondary metabolite isolated from endophytic fungus Phyllosticta capitalensis[1].
Borofalan can be used for Boron neutron capture therapy (BNCT). Borofalan can be used for the research of recurrent or locally advanced head and neck cancer[1].
Pancreastatin (33-49), porcine is a pancreastatin fragment. Pancreastatin is a peptide isolated from porcine pancreas which has insulin-suppressive actions in vitro. Pancreastatin (33-49), porcine enhances the priming effect of glucose[1][2].
Phaseollin is an isoflavonoid phytoalexin that can be isolated from Phaseolus vulgaris . Phaseollin is toxic to bean hypocotyl and endocarp cells, and causes a complete lysis of sheep erythrocytes[1].
Fmoc-Asp(OtBu)-Osu is an aspartic acid derivative[1].
H-Pro-Phe-Thr-Arg-Asn-Tyr-Tyr-Val-Arg-Ala-Val-Leu-His-Leu-OH is an peptide. H-Pro-Phe-Thr-Arg-Asn-Tyr-Tyr-Val-Arg-Ala-Val-Leu-His-Leu-OH can be used for the research of various biochemical studies[1].
Itch-Targeting Compound 1 is an anti-itching agent.
TAT-JIP inhibits the phosphorylation of endogenous c-jun activated by PHA–PMA[1].
Calceolarioside B is a natural product isolated from Stauntonia hexaphylla leaves. Calceolarioside B exhibits significant inhibitory activity against rat lens aldose reductase (RLAR) with an IC50 of 23.99 μM. Calceolarioside B displays inhibitory effect on DPPH radical scavenging activity with an IC50 of 94.60 μM [1].
ITIC, non-fullerene acceptor, is an indacenodithienothiophene-based postfullerene electron acceptor, crystallizes in a profoundly different way as compared to fullerenes.ITIC has a superior thermal stability and undergoes a glass-crystal transition considerably below its high Tg of 180 °C.
Ala-Ser is a biologically active peptide.
3-O-Acetyl-α-boswellic acid suppresses T cell function[1].
AMARA peptide is a substrate for SIK and AMPK.
Evinacumab (REGN1500) is a humanised anti-ANGPTL3 (angiopoietin-like protein 3) monoclonal antibody (IgG4 class antibody). Evinacumab reduces plasma lipids in dyslipidemic mice by blocking ANGPTL3. Evinacumab can be used in studies of homozygous familial hypercholesterolaemia (HoFH), refractory hypercholesterolaemia (both familial and non-familial) and severe hypertriglyceridaemia[1].
Lutonarin is a antioxidant agent that can be isolated from green barley leaves. Lutonarin inhibits malonaldehyde formation from all lipids when in combination with Saponarin (HY-N5083)[1].
H-Val-Arg-OH is a dipeptide consisting of valine and arginine, used in biochemical research[1].
AZD-CO-Ph-PEG4-Ph-CO-AZD is a bis-β-lactam linker can be used for antibody-siRNA conjugate synthesis[1].
Raddeanoside 20 is a triterpenoid isolated from the rhizome of Anemone raddeana. Raddeanoside 20 can suppresse superoxide generation[1].
Antioxidant 1024 (MD 1024) is an antioxidant agent and metal deactivator[1].
L-Alaninol-d3 is the deuterium labeled L-Alaninol[1].
K1 peptide is a high-affinity peptide ligand for GABAA receptor-associated protein (GABARAP)[1].
L-γ-Glutamyl-p-nitroanilide Monohydrate is a glutamic acid derivative[1].
DTSSP Crosslinker disodium is a protein cross-linker containing a disulfide bond. DTSSP Crosslinker disodium can react with sidechains of amino acids that are within close proximity[1][2].
Gamma-Glu-D-Glu is a biologically active peptide.
GRK2 Inhibitor 1 (methyl 5-[2-(5-nitro-2-furyl)vinyl]-2-furoate) is a GRK2 (β-ARK1) inhibitor[1].
1-Naphthaleneacetic acid potassium salt is a synthetic auxin, enhances the organic acid exudation in white lupin plants under phosphorus deficient conditions[1].
((3-Fluorophenyl)sulfonyl)-L-valine is a valine derivative[1].
Maltol, a type of aromatic compound, exists in high concentrations in red ginseng. Maltol is a potent antioxidative agent and typically is used to enhance flavor and preserve food[1].
GaTx2 is a seletive and a high affinity inhibitor of ClC-2 channels with a voltage-dependent apparent KD of ∼20 pM. GaTx2 is a peptide toxin inhibitor from Leiurus quinquestriatus hebraeus venom. GaTx2 is useful in determining the role and the membrane localization of ClC-2 in specific cell types[1].