Date published: 2026-4-23

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KLC1 Inhibitors

KLC1 inhibitors comprise a diverse set of compounds that can modulate the activity of Kinesin Light Chain 1 (KLC1), a crucial component of the kinesin motor protein complex involved in intracellular transport along microtubules. One direct inhibitor, S-Trityl-L-cysteine, specifically targets KLC1, disrupting its interaction with kinesin heavy chain and impeding the transport of cargoes. This direct inhibition offers a precise means of interfering with KLC1-mediated processes. Several indirect inhibitors, such as Oxomemazine, Apicidin, AZD8055, and others, influence KLC1 function by targeting various signaling pathways. Oxomemazine, an antihistamine, modulates the AKT/mTOR pathway, demonstrating the interconnected nature of signaling cascades in regulating KLC1. Histone deacetylase inhibitors like Apicidin and Panobinostat affect the epigenetic control of gene expression, indirectly influencing KLC1 and its associated processes. Inhibitors like AZD8055 and NVP-BKM120 target the mTOR and PI3K/AKT pathways, respectively, indicating the significance of these signaling cascades in KLC1 modulation. Additionally, compounds like Monastrol, GSK690693, MLN8054, and others indirectly inhibit KLC1 by disrupting mitotic spindle dynamics or interfering with cell cycle progression, providing insights into the role of KLC1 in cellular division. Tubacin, an HDAC6 inhibitor, suggests a link between microtubule acetylation and KLC1-mediated intracellular transport. Collectively, these inhibitors offer a comprehensive understanding of the regulatory mechanisms governing KLC1 activity and provide strategies for manipulating intracellular transport processes.

Items 1 to 10 of 11 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

S-Trityl-L-cysteine

2799-07-7sc-202799
sc-202799A
1 g
5 g
$32.00
$66.00
6
(1)

S-Trityl-L-cysteine is a specific inhibitor of Kinesin Light Chain 1 (KLC1). By binding to KLC1, it disrupts the interaction between KLC1 and kinesin heavy chain, inhibiting the transport of cargoes along microtubules. This direct inhibition interferes with the cellular processes that rely on KLC1-mediated transport, suggesting a potential avenue for modulating intracellular trafficking and related functions.

Apicidin

183506-66-3sc-202061
sc-202061A
1 mg
5 mg
$110.00
$343.00
9
(1)

Apicidin is a histone deacetylase inhibitor that indirectly inhibits KLC1. By affecting the epigenetic regulation of gene expression, apicidin influences the expression of proteins involved in intracellular transport, including KLC1.

AZD8055

1009298-09-2sc-364424
sc-364424A
10 mg
50 mg
$163.00
$352.00
12
(2)

AZD8055 is an mTOR inhibitor that indirectly inhibits KLC1. By suppressing the mTOR signaling pathway, AZD8055 interferes with the phosphorylation cascades that regulate KLC1 activity. This indirect modulation highlights the interconnected nature of mTOR signaling and KLC1-mediated processes, providing insights into potential therapeutic strategies to modulate intracellular transport.

Monastrol

254753-54-3sc-202710
sc-202710A
1 mg
5 mg
$120.00
$233.00
10
(1)

Monastrol is a specific kinesin-5 inhibitor that indirectly affects KLC1 function. By perturbing mitotic spindle dynamics, monastrol alters the distribution of KLC1-associated cargoes during cell division. This indirect modulation provides insights into the role of KLC1 in mitosis and suggests potential avenues for disrupting KLC1-mediated processes during cell cycle progression.

GSK 690693

937174-76-0sc-363280
sc-363280A
10 mg
50 mg
$255.00
$1071.00
4
(1)

GSK690693 is an AKT inhibitor that indirectly inhibits KLC1. By suppressing the AKT signaling pathway, GSK690693 interferes with the phosphorylation cascades that regulate KLC1 activity. This indirect modulation highlights the interconnected nature of AKT signaling and KLC1-mediated processes, providing insights into potential therapeutic strategies to modulate intracellular transport.

Panobinostat

404950-80-7sc-208148
10 mg
$200.00
9
(1)

Panobinostat is a histone deacetylase inhibitor that indirectly inhibits KLC1. By affecting the epigenetic regulation of gene expression, panobinostat influences the expression of proteins involved in intracellular transport, including KLC1.

MLN 8054

869363-13-3sc-484828
5 mg
$398.00
(0)

MLN8054 is an Aurora A kinase inhibitor that indirectly inhibits KLC1. By disrupting the cell cycle progression and mitotic spindle assembly, MLN8054 indirectly influences the localization and activity of KLC1-associated cargoes. This modulation provides insights into the role of KLC1 in mitosis and suggests potential avenues for disrupting KLC1-mediated processes during cell division.

BKM120

944396-07-0sc-364437
sc-364437A
sc-364437B
sc-364437C
5 mg
10 mg
25 mg
50 mg
$176.00
$235.00
$281.00
$339.00
9
(0)

BKM120 is a pan-class I PI3K inhibitor that indirectly inhibits KLC1. By suppressing the PI3K/AKT signaling pathway, BKM120 interferes with the phosphorylation cascades that regulate KLC1 activity.

Tris Buffered Saline: 1 L of 1X

sc-362185
1 L
$21.00
3
(2)

Tubacin is a histone deacetylase 6 (HDAC6) inhibitor that indirectly inhibits KLC1. By modulating the acetylation status of microtubules and affecting the function of motor proteins, including kinesins, tubacin influences the dynamics of KLC1-mediated intracellular transport.

AZD5363

1143532-39-1sc-503190
5 mg
$309.00
(0)

AZD5363 is an AKT inhibitor that indirectly inhibits KLC1. By suppressing the AKT signaling pathway, AZD5363 interferes with the phosphorylation cascades that regulate KLC1 activity. This indirect modulation highlights the interconnected nature of AKT signaling and KLC1-mediated processes, providing insights into potential therapeutic strategies to modulate intracellular transport.