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19 results for "Cell Adhesion Inhibitors Small Molecules and Peptides" in Products

Cell Adhesion Inhibitors: Small Molecules and Peptides

Selective inhibitor of P-selectin-mediated cell adhesion

Chemical Name: 3-[7-(2,4-Dimethoxyphenyl)-2,3,6,7-tetrahydro-1,4-thiazepin-5-yl]-4-hydroxy-6-methyl-2H-pyran-2-one
Purity: ≥97% (HPLC)
Selective inhibitor of P-selectin-mediated cell adhesion

Sialic acid analog; sialyltransferase inhibitor

Chemical Name: 5-(Acetylamino)-3,5-dideoxy-3-fluoro-D-erythro-α-L-manno-2-nonulopyranosonic acid methyl ester 2,4,7,8,9-pentaacetate
Purity: ≥97% (HPLC)
Sialic acid analog; sialyltransferase inhibitor

Anticoagulant

Heparin sodium salt | CAS No. 9041-08-1 | Anticoagulant

Potent integrin inhibitor (αvβ3/αvβ6); also improves stem cell attachment in 3D cell culture scaffolds

Purity: ≥95% (HPLC)
Potent integrin inhibitor (αVβ3/αVβ5); also improves stem cell attachment in 3D cell culture scaffolds

Heparin sulfate antagonist

Chemical Name: N,N'-Bis(4-amino-2-methyl-6-quinolinyl)urea dihydrochloride
Purity: ≥98% (HPLC)
Heparin sulfate antagonist

αVβ3 and glycoprotein IIb/IIIa (integrin αIIbβ3) inhibitor

Purity: ≥95% (HPLC)
αVβ3 and glycoprotein IIb/IIIa (integrin αIIbβ3) inhibitor

Potent and selective α1β1 inhibitor

Purity: ≥95% (HPLC)
Potent and selective α1β1 inhibitor

Antiangiogenic. Heparanase inhibitor

Chemical Name: 2-[4-[[3-(4-Bromophenyl)-1-oxo-2-propenyl]amino]-3-fluorophenyl]-5-benzoxazoleacetic acid
Purity: ≥97% (HPLC)
Antiangiogenic. Heparanase inhibitor

Potent inhibitor of the LFA-1/ICAM interaction

Chemical Name: 6-[(5S,9R)-9-(4-Cyanophenyl)-3-(3,5-dichlorophenyl)-1-methyl-2,4-dioxo-1,3,7-triazaspiro[4,4]non-7-yl]-3-pyridinecarboxylic acid
Purity: ≥98% (HPLC)
Potent inhibitor of the LFA-1/ICAM interaction

Integrin binding sequence; inhibits integrin receptor function

Purity: ≥95% (HPLC)
Integrin binding sequence; inhibits integrin receptor function

Selective α4β1 (VLA-4) inhibitor

Purity: ≥95% (HPLC)
Selective α4β1 (VLA-4) inhibitor

Potent inhibitor of the LFA-1/ICAM-1 interaction

Chemical Name: (2E)-1-(4-Acetyl-1-piperazinyl)-3-[4-[[2-(1-methylethyl)phenyl]thio]-3-nitrophenyl]-2-propen-1-one
Purity: ≥98% (HPLC)
Potent inhibitor of the LFA-1/ICAM-1 interaction

Potent α2β1 inhibitor; displays antithrombotic activity in vivo

Chemical Name: N-[[(4R)-5,5-Dimethyl-3-(phenylsulfonyl)-4-thiazolidinyl]carbonyl]-3-[[[(phenylmethyl)amino]carbonyl]amino]-L-alanine
Purity: ≥98% (HPLC)
Potent α2β1 inhibitor; displays antithrombotic activity in vivo

Annexin/lipocortin 1-mimetic; inhibits leukocyte extravasation

Purity: ≥95% (HPLC)
Annexin/lipocortin 1-mimetic; inhibits leukocyte extravasation

Selective inhibitor of E-selectin and ICAM-1 expression

Chemical Name: 4-[(4-Methylphenyl)thio]thieno[2,3-c]pyridine-2-carboxamide
Purity: ≥98% (HPLC)
Selective inhibitor of E-selectin and ICAM-1 expression

Disrupts MTDH and SND1 interaction, enhances immune surveillance

Chemical Name: 5-Chloro-2-methoxy-N-(2-methyl[1,2,4]triazolo[1,5-a]pyridin-8-yl)benzenesulfonamide
Purity: ≥98% (HPLC)
Disrupts MTDH and SND1 interaction, enhances immune surveillance

α4β1 (VLA-4) antagonist

Chemical Name: 1-[[(3S)-4-[2-[4-[[[(2-Methylphenyl)amino]carbonyl]amino]phenyl]acety]l-3-morpholinyl]carbonyl]-4-piperidinediacetic acid
Purity: ≥98% (HPLC)
α4β1 (VLA-4) antagonist

ctRAGE-DIAPH1 interaction antagonist; reduces inflammatory signaling in diabetic mice

Chemical Name: N-[4-[7-Cyano-4-(4-morpholinylmethyl)-2-quinolinyl]phenyl]acetamide
Purity: ≥98% (HPLC)
ctRAGE-DIAPH1 interaction antagonist; reduces inflammatory signaling in diabetic mice

Glycoprotein IIb/IIIa (integrin αIIbβ3) receptor antagonist. Antithrombotic

Chemical Name: 4-[4-[4-(Aminoiminomethyl)phenyl]-1-piperazinyl]-1-piperidineacetic acid trihydrochloride
Purity: ≥98% (HPLC)
Glycoprotein IIb/IIIa (integrin αIIbβ3) receptor antagonist. Antithrombotic
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