Date published: 2026-5-16

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SYCE1L Inhibitors

SYCE1L inhibitors are a class of chemical compounds that specifically target and inhibit the activity of SYCE1L (Synaptonemal Complex Central Element Protein 1-Like), a protein that is part of the synaptonemal complex (SC). The synaptonemal complex plays a crucial role in the pairing and synapsis of homologous chromosomes during meiosis, a process necessary for the accurate segregation of chromosomes into gametes. SYCE1L is structurally similar to SYCE1, another central element protein in the SC, and is believed to play a role in maintaining the integrity of chromosome alignment and cohesion during meiotic prophase. Inhibitors of SYCE1L work by disrupting its function within the synaptonemal complex, thereby affecting the stabilization and assembly of the SC, which is critical for homologous chromosome synapsis and recombination.

The chemical structure and mechanisms of SYCE1L inhibitors vary, depending on how they interact with the protein. Some inhibitors may bind directly to SYCE1L, preventing it from engaging with other structural components of the synaptonemal complex, such as SYCE1 or other central element proteins. Others may act by altering the conformation of SYCE1L, inhibiting its ability to support the structural framework necessary for proper chromosome pairing. Inhibition of SYCE1L affects the overall architecture of the synaptonemal complex, potentially leading to disruptions in chromosome alignment, recombination, and separation. Studying SYCE1L inhibitors provides key insights into the molecular mechanisms that regulate meiotic chromosome dynamics, offering a deeper understanding of the structural components involved in chromosomal synapsis. This research expands the knowledge of how precise protein interactions within the synaptonemal complex contribute to the fidelity of meiosis and the maintenance of genetic stability during reproduction.

SEE ALSO...

Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

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)

A microtubule-depolymerizing drug. Nocodazole could indirectly impact SYCE1L activity by disrupting microtubule dynamics essential for meiosis.

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)

An anti-inflammatory agent that also affects microtubule polymerization. Colchicine could indirectly influence SYCE1L by altering the cytoskeletal dynamics critical for meiotic processes.

Letrozole

112809-51-5sc-204791
sc-204791A
25 mg
50 mg
$87.00
$147.00
5
(1)

An aromatase inhibitor used in infertility. Letrozole could indirectly affect SYCE1L by modulating estrogen levels, thereby influencing meiotic processes.

Atrazine

1912-24-9sc-210846
5 g
$165.00
1
(1)

An herbicide known to disrupt endocrine function. Atrazine could indirectly affect SYCE1L through its impact on hormonal regulation of reproductive processes, including meiosis.

Bisphenol A

80-05-7sc-391751
sc-391751A
100 mg
10 g
$300.00
$490.00
5
(0)

An endocrine disruptor that can affect reproductive health. BPA could indirectly impact SYCE1L by influencing hormonal pathways critical for meiosis.

Genistein

446-72-0sc-3515
sc-3515A
sc-3515B
sc-3515C
sc-3515D
sc-3515E
sc-3515F
100 mg
500 mg
1 g
5 g
10 g
25 g
100 g
$45.00
$164.00
$200.00
$402.00
$575.00
$981.00
$2031.00
46
(1)

A phytoestrogen that can modulate estrogenic activity. Genistein could indirectly influence SYCE1L function by affecting hormonal regulation related to reproductive processes.

Ketoconazole

65277-42-1sc-200496
sc-200496A
50 mg
500 mg
$63.00
$265.00
21
(1)

An antifungal agent in research that can affect steroid biosynthesis. Ketoconazole could indirectly impact SYCE1L by altering steroid hormone levels and potentially influencing meiosis.

5-Azacytidine

320-67-2sc-221003
500 mg
$280.00
4
(1)

A DNA methyltransferase inhibitor that can affect gene expression. 5-Azacytidine could indirectly influence SYCE1L activity by modulating the epigenetic landscape during meiosis.