C07K4/00

HETEROARYL SULFONE-BASED CONJUGATION HANDLES, METHODS FOR THEIR PREPARATION, AND THEIR USE IN SYNTHESIZING ANTIBODY DRUG CONJUGATES

The present invention is directed to novel heteroaryl sulfone-based conjugation handles of the formula: (wherein R.sup.1, R.sup.2, Het, D, E, X, Y, Z, m, n, p, q, r, s and t are as defined herein), methods for their preparation, their use in synthesizing antibody drig conjugates, and the resulting antibody drig conjugates made with components having heteroaryl sulfone-based conjugation handles.

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Antimicrobial peptides and compositions, methods, articles and kits relating thereto

Peptides are described herein, in particular peptides having antimicrobial properties, as are compositions, articles, and kits comprising such peptides, and methods for using the peptides.

Antimicrobial peptides and compositions, methods, articles and kits relating thereto

Peptides are described herein, in particular peptides having antimicrobial properties, as are compositions, articles, and kits comprising such peptides, and methods for using the peptides.

Methods for the treatment of glaucoma and age-related macular degeneration by a peptide D-TRP-AIB
10987400 · 2021-04-27 · ·

Methods for the prevention and treatment of ocular disorders, in particular glaucoma, through blocking the toxic effects of β-amyloid (Aβ) derivatives, and pharmaceutical compositions for effecting such prevention and treatment thereof.

Composition and Methods of Controllable Co-Coupling Polypeptide Nanoparticle Delivery System for Nucleic Acid Therapeutics
20210162067 · 2021-06-03 ·

The present invention provides certain peptides and polypeptides useful in the preparation of nanoparticles for delivering nucleic acids and pharmaceutical drugs to mammalian cells and to humans and other mammals. It further provides methods for making the peptides, polypeptides, and nanoparticles and methods for using the nanoparticles.

Composition and Methods of Controllable Co-Coupling Polypeptide Nanoparticle Delivery System for Nucleic Acid Therapeutics
20210162067 · 2021-06-03 ·

The present invention provides certain peptides and polypeptides useful in the preparation of nanoparticles for delivering nucleic acids and pharmaceutical drugs to mammalian cells and to humans and other mammals. It further provides methods for making the peptides, polypeptides, and nanoparticles and methods for using the nanoparticles.

PEPTIDE TAG AND TAGGED PROTEIN INCLUDING SAME

A peptide comprising the sequence shown below is added as a peptide tag to a useful protein, followed by allowing its expression.


X.sub.m(PY.sub.n).sub.qPZ.sub.r

In this formula, X, Y, and Z each represent an amino acid residue independently selected from the group consisting of R, G, S, K, T, L, N, Q, and H, with the proviso that at least one Y represents K, L, N, Q, H, or R. m represents an integer of 0 to 5; n represents 1, 2, or 3; q represents an integer of 1 to 10; and r represents an integer of 0 to 10.

Prelyophilized, lyophilized and reconstituted formulations comprising TAT-NR2B9C with d-amino acids, histidine and trehalose
10912817 · 2021-02-09 · ·

The present invention provides lyophilized formulations of active agents, particularly of TAT-NR2B9c. TAT-NR2B9c has shown promise for treating stroke, aneurysm, subarachnoid hemorrhage and other neurological or neurotraumatic conditions. Such formulations are stable at room temperature thus facilitating maintenance of supplies of such a formulation in ambulances for administration at the scene of illness or accident or in transit to a hospital.

PEPTIDES WITH ANTI-CANCER ACTIVITY
20210008159 · 2021-01-14 ·

The peptides of the invention are of formula (I) or (IV). The peptides of the invention are useful in the treatment of cancer.

PEPTIDES WITH ANTI-CANCER ACTIVITY
20210008159 · 2021-01-14 ·

The peptides of the invention are of formula (I) or (IV). The peptides of the invention are useful in the treatment of cancer.