(Q43448790)

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Anti-HIV-1 peptides derived from partial amino acid sequences of CC-chemokine RANTES. Regulated upon activation, normal T-cell expressed and secreted

scientific article published in December 2002

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Europe PubMed Central

PubMed publication ID

23 November 2017

Anti-HIV-1 peptides derived from partial amino acid sequences of CC-chemokine RANTES. Regulated upon activation, normal T-cell expressed and secreted (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

5

object named as

Naoki Yamamoto

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

4

object named as

Keisuke Kurita

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

author name string

Yasuhiro Nishiyama

1

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

Tsutomu Murakami

2

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

Suguru Shikama

3

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

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publication date

1 December 2002

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Europe PubMed Central

PubMed publication ID

23 November 2017

Bioorganic & Medicinal Chemistry

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Europe PubMed Central

PubMed publication ID

23 November 2017

10

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Europe PubMed Central

PubMed publication ID

23 November 2017

12

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

4113-4117

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

Co-receptor use by HIV and inhibition of HIV infection by chemokine receptor ligands

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Identification of a major co-receptor for primary isolates of HIV-1

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HIV-1 entry into CD4+ cells is mediated by the chemokine receptor CC-CKR-5

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HIV-1 Entry Cofactor: Functional cDNA Cloning of a Seven-Transmembrane, G Protein-Coupled Receptor

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Identification of RANTES, MIP-1 alpha, and MIP-1 beta as the major HIV-suppressive factors produced by CD8+ T cells

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The CXC chemokine SDF-1 is the ligand for LESTR/fusin and prevents infection by T-cell-line-adapted HIV-1

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HIV blocked by chemokine antagonist

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Potent inhibition of HIV-1 infectivity in macrophages and lymphocytes by a novel CCR5 antagonist.

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Amino-terminal truncation of chemokines by CD26/dipeptidyl-peptidase IV. Conversion of RANTES into a potent inhibitor of monocyte chemotaxis and HIV-1-infection.

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CD26-processed RANTES(3-68), but not intact RANTES, has potent anti-HIV-1 activity.

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A small-molecule, nonpeptide CCR5 antagonist with highly potent and selective anti-HIV-1 activity

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Piperazine-based CCR5 antagonists as HIV-1 inhibitors. I: 2(S)-methyl piperazine as a key pharmacophore element

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Antagonists of the human CCR5 receptor as anti-HIV-1 agents. part 1: discovery and initial structure-activity relationships for 1 -amino-2-phenyl-4-(piperidin-1-yl)butanes

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Antagonists of the human CCR5 receptor as anti-HIV-1 agents. Part 2: structure-activity relationships for substituted 2-Aryl-1-[N-(methyl)-N-(phenylsulfonyl)amino]-4-(piperidin-1-yl)butanes

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Novel low molecular weight spirodiketopiperazine derivatives potently inhibit R5 HIV-1 infection through their antagonistic effects on CCR5.

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AMD3100, a small molecule inhibitor of HIV-1 entry via the CXCR4 co-receptor.

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A small molecule CXCR4 inhibitor that blocks T cell line-tropic HIV-1 infection

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A small-molecule inhibitor directed against the chemokine receptor CXCR4 prevents its use as an HIV-1 coreceptor

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Cyclic zinc-dithiocarbamate-S,S'-dioxide blocks CXCR4-mediated HIV-1 infection

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Cell adhesive sequences in mouse laminin beta1 chain

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Inhibition of purified p21ras farnesyl:protein transferase by Cys-AAX tetrapeptides

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Synthetic peptides of CD66a stimulate neutrophil adhesion to endothelial cells

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Genetic subtype-independent inhibition of human immunodeficiency virus type 1 replication by CC and CXC chemokines.

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Synthesis of some peptides corresponding to the active region of RANTES for chemotaxis and evaluation of their anti-human immunodeficiency virus-1 activity

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Low-molecular-weight anti-HIV-1 peptides from the amino-terminal sequence of RANTES: possible lead compounds for coreceptor-directed anti-HIV-1 agents

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Biology of the rantes/sis cytokine family

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Peptides from the Amino Terminus of Rantes Cause Chemotaxis of Human T-Lymphocytes

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Anti-human immunodeficiency virus activity of a novel synthetic peptide, T22 ([Tyr-5,12, Lys-7]polyphemusin II): a possible inhibitor of virus-cell fusion

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Distinct but overlapping epitopes for the interaction of a CC-chemokine with CCR1, CCR3 and CCR5

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Functional genomics Double-stranded RNA poses puzzle

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A new monoclonal antibody, mAb 4A12, identifies a role for the glycosaminoglycan (GAG) binding domain of RANTES in the antiviral effect against HIV-1 and intracellular Ca2+ signaling

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Soluble complexes of regulated upon activation, normal T cells expressed and secreted (RANTES) and glycosaminoglycans suppress HIV-1 infection but do not induce Ca(2+) signaling

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Optimal inhibition of X4 HIV isolates by the CXC chemokine stromal cell-derived factor 1 alpha requires interaction with cell surface heparan sulfate proteoglycans

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Host cyclophilin A mediates HIV-1 attachment to target cells via heparans

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Attachment of C-terminus of SDF-1 enhances the biological activity of its N-terminal peptide

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Identifiers

10.1016/S0968-0896(02)00271-7

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

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