peptide 74

Peptide 74 is a synthetic peptide. It also inhibits the activated form of this enzyme.

Bax BH3 peptide (55-74), wild type is a 20-amino acid peptide (Bax 1) known for its apoptosis-inducing capability in various cell line models.

Human Prokineticin-2 peptide (28-74, 96-128) is a truncated version of human Prokineticin-2 (PROK2), derived from SEQ NO:6 in Patent WO2002036625A2, and can be used for relevant research in the life sciences field. Prokineticin-2 (human) is a regulatory hypothalamic neuropeptide that plays a role in food intake, thermoregulation, and energy metabolism.

Oligopeptide-74, a bioactive peptide known for promoting hair growth, is utilized as a cosmetic ingredient [1].

Beta-Sheet Breaker Peptide iAβ5 Acetate (C33H43N5O8) inhibit amyloidogenesis in rat brain models.

β-Amyloid (1-42), rat/mouse TFA is a 42-amino-acid polypeptide fragment that exhibits neurotoxicity to hippocampal slices and is commonly used to establish Alzheimer's disease models for related research.

Tyr-α-CGRP is an N-terminal extended tyrosinated analogue of α-calcitonin gene-related peptide . It binds to amylin receptors AMY1 and AMY3 in COS-7 cells expressing the human receptors (IC50s = 141 and 1.86 nM, respectively). Tyr-α-CGRP also binds to and stimulates cAMP accumulation in rat L6 myocytes (IC50 = 4 nM; EC50 = 12 nM). It also binds to rat brain and spleen membrane preparations (IC50s = 0.2 and 0.5 nM, respectively), induces positive chronotropic and inotropic effects in isolated right and left guinea pig atria (EC50s = 282 and 74 nM, respectively), and inhibits the twitch response in rat vas deferens (EC50 = 1.9 nM).

MLCK inhibitor peptide 18 acetate is a selective competitive inhibitor of myosin light chain kinase (IC50 = 50 nM). Displays 4000-fold selectivity over CaM kinase II and does not inhibit PKA. Cell permeable.

Peptide 78 is identical to peptide 74 except that serine replaces cysteine. It does not inhibit 72-kDa type IV collagenase.

CXCL9(74-103) is a derivative peptide of CXCL9 that binds with high affinity to glycosaminoglycans (GAGs). It exhibits anti-angiogenic properties by reducing angiogenesis mediated by EGF, VEGF165, and FGF-2 in vitro, without causing cytotoxicity.