Date published: 2026-2-14

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CCDC65 Inhibitors

The chemical class of CCDC65 (Dynein Regulatory Complex Subunit 2) Inhibitors, as compiled, is focused on compounds that influence microtubule dynamics or motor protein functions, which are crucial for ciliary and flagellar motility. These inhibitors target processes that are indirectly related to CCDC65's role in the assembly and function of the nexin-dynein regulatory complex (N-DRC) and its interaction with microtubules. Compounds like Taxol, Vinblastine, and Colchicine are known for their ability to modulate microtubule dynamics by either stabilizing or disrupting microtubule assembly. Since CCDC65 is involved in microtubule organization within cilia and flagella, altering the stability and dynamics of microtubules can indirectly influence the function of CCDC65. These changes in microtubule dynamics can affect the alignment, integrity, and motility of cilia and flagella, thereby impacting the cellular processes in which these structures are involved.

Additionally, inhibitors like Nocodazole and Vincristine specifically disrupt microtubule polymerization, which could have implications for the microtubule-dependent roles of CCDC65. In contrast, compounds such as Eribulin and Docetaxel stabilize microtubules, offering a different mechanism by which the microtubule-related functions of CCDC65 could be influenced. Furthermore, the inclusion of Kinesin Spindle Protein (KSP) inhibitors, dynein motor inhibitors, and specific kinase inhibitors like Alisertib reflects the complexity of the cellular machinery involved in microtubule dynamics and motor protein functions. By targeting these components, the inhibitors can indirectly modulate the environment in which CCDC65 operates, affecting its function in ciliary and flagellar motility. In summary, this chemical class provides an indirect approach to influencing CCDC65 function by targeting related microtubule dynamics and motor protein functions. Understanding the interplay between these inhibitors and the microtubule machinery is essential for exploring research related to diseases and disorders involving ciliary and flagellar dysfunction.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Taxol

33069-62-4sc-201439D
sc-201439
sc-201439A
sc-201439E
sc-201439B
sc-201439C
1 mg
5 mg
25 mg
100 mg
250 mg
1 g
$41.00
$74.00
$221.00
$247.00
$738.00
$1220.00
39
(2)

Taxol stabilizes microtubules, potentially affecting CCDC65's role in microtubule organization in cilia and flagella.

Vinblastine

865-21-4sc-491749
sc-491749A
sc-491749B
sc-491749C
sc-491749D
10 mg
50 mg
100 mg
500 mg
1 g
$102.00
$235.00
$459.00
$1749.00
$2958.00
4
(0)

Vinblastine disrupts microtubule assembly, potentially influencing CCDC65-related microtubule dynamics.

Colchicine

64-86-8sc-203005
sc-203005A
sc-203005B
sc-203005C
sc-203005D
sc-203005E
1 g
5 g
50 g
100 g
500 g
1 kg
$100.00
$321.00
$2289.00
$4484.00
$18207.00
$34749.00
3
(2)

Colchicine binds to tubulin, inhibiting microtubule polymerization, and may indirectly affect CCDC65 function.

Nocodazole

31430-18-9sc-3518B
sc-3518
sc-3518C
sc-3518A
5 mg
10 mg
25 mg
50 mg
$59.00
$85.00
$143.00
$247.00
38
(2)

Nocodazole disrupts microtubule polymerization, potentially influencing the microtubule-dependent processes involving CCDC65.

Eribulin

253128-41-5sc-507547
5 mg
$865.00
(0)

Eribulin inhibits microtubule growth, potentially affecting CCDC65's role in microtubule organization.

Docetaxel

114977-28-5sc-201436
sc-201436A
sc-201436B
5 mg
25 mg
250 mg
$87.00
$332.00
$1093.00
16
(1)

Docetaxel stabilizes microtubules, potentially impacting the microtubule dynamics regulated by CCDC65.

Ispinesib

336113-53-2sc-364747
10 mg
$505.00
(0)

KSP inhibitors like Ispinesib disrupt mitotic spindle dynamics, potentially influencing CCDC65-related microtubule functions.

MLN8237

1028486-01-2sc-394162
5 mg
$220.00
(0)

Alisertib inhibits aurora kinase A, involved in microtubule organization, potentially impacting CCDC65 function.

Monastrol

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

Monastrol is a kinesin-5 inhibitor, potentially affecting microtubule dynamics relevant to CCDC65's function.