Date published: 2025-12-20

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ABR Inhibitors

ABR inhibitors encompass a diverse array of chemical compounds that indirectly suppress the functional activity of ABR through targeted actions on specific signaling pathways that ABR is known to interact with. For instance, Staurosporine and Securinine function through the inhibition of protein kinases and alteration of GABA receptor activity, respectively, which both culminate in the modulation of Rho GTPases signaling processes controlled by ABR. The Rho GTPases are critical for various cellular functions, and ABR regulates these through its GTPase activating protein activity. Consequently, by inhibiting kinases that phosphorylate ABR substrates or altering Rho GTPase signaling, these compounds effectively diminish ABR's regulatory role. Similarly, the Rho Kinase Inhibitor Y-27632 and the PI3K inhibitor LY294002 both act on enzymes in pathways that intersect with those regulated by ABR, leading to a net decrease in ABR's signaling efficacy.

Further influencing ABR's activity are compounds like ML141 and NSC23766, which act on Cdc42 and Rac1, respectively, two members of the Rho GTPase family that ABR is known to affect. By inhibiting these GTPases, ML141 and NSC23766 attenuate the downstream effects thatABR inhibitors encompass a diverse array of chemical compounds that indirectly suppress the functional activity of ABR through targeted actions on specific signaling pathways that ABR is known to interact with. For instance, Staurosporine and Securinine function through the inhibition of protein kinases and alteration of GABA receptor activity, respectively, which both culminate in the modulation of Rho GTPases signaling processes controlled by ABR. The Rho GTPases are critical for various cellular functions, and ABR regulates these through its GTPase activating protein activity. Consequently, by inhibiting kinases that phosphorylate ABR substrates or altering Rho GTPase signaling, these compounds effectively diminish ABR's regulatory role. Similarly, the Rho Kinase Inhibitor Y-27632 and the PI3K inhibitor LY294002 both act on enzymes in pathways that intersect with those regulated by ABR, leading to a net decrease in ABR's signaling efficacy.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Staurosporine

62996-74-1sc-3510
sc-3510A
sc-3510B
100 µg
1 mg
5 mg
$82.00
$150.00
$388.00
113
(4)

Staurosporine, a kinase inhibitor, indirectly inhibits ABR by targeting protein kinases that phosphorylate ABR substrates, thereby reducing ABR's ability to act as a GTPase activating protein for Rho family members.

NSC 23766

733767-34-5sc-204823
sc-204823A
10 mg
50 mg
$148.00
$597.00
75
(4)

NSC23766 disrupts Rac1 binding and activation, a process that is regulated by ABR. The inhibition of Rac1 can lead to the functional suppression of ABR's downstream signaling.

ML 141

71203-35-5sc-362768
sc-362768A
5 mg
25 mg
$134.00
$502.00
7
(1)

ML141 is a potent inhibitor of Cdc42 GTPase, and since ABR functions as a GTPase activating protein, inhibition of Cdc42 can reduce ABR-mediated signaling pathways.

Y-27632, free base

146986-50-7sc-3536
sc-3536A
5 mg
50 mg
$182.00
$693.00
88
(1)

Y-27632 inhibits Rho-associated kinase which works downstream of the Rho family of GTPases; by inhibiting this kinase, the signaling cascade in which ABR participates is diminished.

LY 294002

154447-36-6sc-201426
sc-201426A
5 mg
25 mg
$121.00
$392.00
148
(1)

LY294002 is a PI3K inhibitor that, when PI3K is inhibited, can suppress the downstream signaling involving ABR, as ABR is known to interact with PI3K-related pathways.

Lovastatin

75330-75-5sc-200850
sc-200850A
sc-200850B
5 mg
25 mg
100 mg
$28.00
$88.00
$332.00
12
(1)

Lovastatin inhibits HMG-CoA reductase leading to reduced prenylation of proteins. As a result, it can impair the proper localization and function of Rho GTPases, therefore affecting ABR signaling.

Lysophosphatidic Acid

325465-93-8sc-201053
sc-201053A
5 mg
25 mg
$96.00
$334.00
50
(3)

LPA acts through its receptors to activate Rho GTPases and can influence the cellular pathways regulated by ABR, potentially leading to reduced ABR activity through altered pathway dynamics.