Date published: 2026-5-16

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LOH12CR1 Inhibitors

LOH12CR1 inhibitors belong to a class of chemical compounds designed to target and modulate the activity of the LOH12CR1 protein, which is also known as Loss of Heterozygosity in Chromosome 12 Region 1. LOH12CR1 is a protein with a poorly characterized function, and it is often associated with genomic alterations in a specific region of chromosome 12. This region, known as 12q22-24, is frequently subject to loss of heterozygosity (LOH) in various types of cancer, indicating its potential involvement in tumorigenesis. LOH12CR1 is one of the genes located within this region, and while its exact role in cellular processes is not fully understood, it has been the subject of interest in cancer research. Inhibitors of LOH12CR1 are developed to interfere with its function or activity, potentially influencing the cellular processes associated with LOH12CR1 and the broader implications in cancer biology.

The mechanisms by which LOH12CR1 inhibitors function can vary based on their chemical structures and binding properties. Some inhibitors may directly interact with LOH12CR1, disrupting its potential functions or interactions with other cellular components. Others may modulate the stability or conformation of LOH12CR1, affecting its participation in cellular processes. By inhibiting LOH12CR1, these compounds have the potential to impact the cellular pathways associated with this protein, particularly in the context of cancer-associated genomic alterations. Ongoing research in this field aims to elucidate the precise role of LOH12CR1 in cellular biology and the consequences of its inhibition, contributing to our understanding of its significance in the context of cancer and genomic stability.

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Items 1 to 10 of 12 total

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Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Hydroxyurea

127-07-1sc-29061
sc-29061A
5 g
25 g
$78.00
$260.00
18
(1)

Hydroxyurea may influence LOH12CR1 expression by disrupting DNA synthesis and cell cycle progression.

2′-Deoxy-2′,2′-difluorocytidine

95058-81-4sc-275523
sc-275523A
1 g
5 g
$56.00
$128.00
(1)

Gemcitabine, a nucleoside analog, could potentially affect LOH12CR1 expression through its role in inhibiting DNA replication.

Cisplatin

15663-27-1sc-200896
sc-200896A
100 mg
500 mg
$138.00
$380.00
101
(4)

Cisplatin might impact LOH12CR1 expression by causing DNA damage and affecting cell cycle checkpoints.

Etoposide (VP-16)

33419-42-0sc-3512B
sc-3512
sc-3512A
10 mg
100 mg
500 mg
$51.00
$231.00
$523.00
63
(1)

Etoposide, a topoisomerase inhibitor, may modulate LOH12CR1 expression by interfering with DNA repair mechanisms.

Bleomycin

11056-06-7sc-507293
5 mg
$275.00
5
(0)

Bleomycin, known for causing DNA breaks, could influence LOH12CR1 expression through its effects on DNA repair processes.

Doxorubicin

23214-92-8sc-280681
sc-280681A
1 mg
5 mg
$176.00
$426.00
43
(3)

Doxorubicin might alter LOH12CR1 expression by inducing DNA damage and apoptosis.

Methotrexate

59-05-2sc-3507
sc-3507A
100 mg
500 mg
$94.00
$213.00
33
(5)

Methotrexate, a dihydrofolate reductase inhibitor, may affect LOH12CR1 expression by disrupting nucleotide synthesis and DNA replication.

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, a microtubule inhibitor, could potentially modulate LOH12CR1 expression by disrupting mitotic spindles and cell division.

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)

Paclitaxel, another microtubule-targeting drug, might influence LOH12CR1 expression by affecting cell cycle progression and mitosis.

Tamoxifen

10540-29-1sc-208414
2.5 g
$272.00
18
(2)

Tamoxifen, an estrogen receptor modulator, may impact LOH12CR1 expression in hormone-responsive tissues and cancers.