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21 results for "Cell Adhesion Inhibitors" in Products

Cell Adhesion Inhibitors

Anticoagulant

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

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

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

Annexin/lipocortin 1-mimetic; inhibits leukocyte extravasation

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

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%
Selective inhibitor of P-selectin-mediated cell adhesion

Selective α4β1 (VLA-4) inhibitor

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

Integrin binding sequence; inhibits integrin receptor function

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

Fluorescent ligand for α4β1 (VLA-4)

Purity:
≥90%
Fluorescent ligand for α4β1 (VLA-4)

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%
Sialic acid analog; sialyltransferase inhibitor

Selective inhibitor of E-selectin and ICAM-1 expression

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

Antiangiogenic. Heparanase inhibitor

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

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%
Potent α2β1 inhibitor; displays antithrombotic activity in vivo

Potent and selective α1β1 inhibitor

Purity:
≥95%
Potent and selective α1β1 inhibitor

αVβ3 and glycoprotein IIb/IIIa (integrin αIIbβ3) inhibitor

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

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%
α4β1 (VLA-4) antagonist

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

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%
Potent inhibitor of the LFA-1/ICAM interaction

Heparin sulfate antagonist

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

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%
Disrupts MTDH and SND1 interaction, enhances immune surveillance

High affinity antagonist of RAGE

Chemical Name:
4-Chloro-N-cyclohexyl-N-(phenylmethyl)benzamide
Purity:
≥98%
High affinity antagonist of RAGE

α2,8-linked polysialic acid biosynthesis attenuator

Alternate Names:
8-Keto-Neu5Ac
Chemical Name:
(S)-1-((2R,3R,4S,6R)-3-Acetamido-4,6-diacetoxy-6-((pentyloxy)carbonyl)tetrahydro-2H-pyran-2-yl)-2-oxopropane-1,3-diyl diacetate
Purity:
≥90%
α2,8-linked polysialic acid biosynthesis attenuator

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

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