Survivin
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Survivin is the smallest member of the inhibitor of apoptosis (IAP) protein family, a family of highly conserved cell apoptosis inhibitors characterized by the presence of a zinc-binding fold (the baculoviral IAP repeat), that is comprised of a single N-terminal BIR domain, a long C-terminal α-helix coiled region and a dimeric arrangement. Survivin is a bifunctional protein, apart from its ability to inhibit apoptosis, which also plays an essential role in proper cell division. Survivin is not expressed in most normal and terminally differentiated adult tissues but expressed in fetal tissues, where its expression is cell cycle-regulated and peaks at mitosis.
Products Related to Survivin(12)
- GC35758Cucurbitacin IIaCAS: 58546-34-2Purity: >99.00%
Cucurbitacin IIa is a triterpene isolated from Hemsleya amalils Diels, induces apoptosis of cancer cells, reduces expression of survivin, reduces phospho-Histone H3 and increases cleaved PARP in cancer cells.
- GC69884Shepherdin (79-87) (TFA)Purity: >98.00%
Shepherdin (79-87) TFA is a 79 to 87 amino acid fragment of Shepherdin. Shepherdin is a peptide antagonist of the Hsp90-Survivin complex and has anti-tumor activity.
- GC80875PROTAC survivin degrader-1CAS: 3079079-69-6Purity: >98%
PROTAC survivin degrader-1 is an orally active, CNS-penetrant survivin -targeting PROTAC.
| Catalog No. | Product Name | CAS No. | Purity | Structure |
|---|---|---|---|---|
| GC13107 | YM155 | 781661-94-7 | >98.00% | |
YM155, a small imidazolium-based compound, potently inhibits survivin promoter activity with an IC 50 value of 0.54nM. | ||||
| GC15632 | YM-155 hydrochloride | 355406-09-6 | >98% | |
A survivin inhibitor | ||||
| GC33097 | GDP366 | 501698-03-9 | >99.50% | |
GDP366, a dual inhibitor of survivin and Op18, induces cell growth inhibition, cellular senescence and mitotic catastrophe in human cancer cells. | ||||
| GC35758 | Cucurbitacin IIa | 58546-34-2 | >99.00% | |
Cucurbitacin IIa is a triterpene isolated from Hemsleya amalils Diels, induces apoptosis of cancer cells, reduces expression of survivin, reduces phospho-Histone H3 and increases cleaved PARP in cancer cells. | ||||
| GC60229 | LQZ-7I | 195822-23-2 | >99.50% | |
LQZ-7I is a survivin-targeting inhibitor. LQZ-7I inhibits survivin dimerization. LQZ-7I orally effectively inhibits xenograft tumor growth and induces survivin loss in tumors. | ||||
| GC69884 | Shepherdin (79-87) (TFA) | - | >98.00% | |
Shepherdin (79-87) TFA is a 79 to 87 amino acid fragment of Shepherdin. Shepherdin is a peptide antagonist of the Hsp90-Survivin complex and has anti-tumor activity. | ||||
| GC72933 | LQZ-7F | 354543-09-2 | >97.00% | |
LQZ-7F, a survivin dimerization inhibitor, induces spontaneous apoptosis and synergizes with Docetaxel in prostate cancer cells. | ||||
| GC73986 | MX106-4C | - | >98.00% | |
MX106-4C is a survivin inhibitor that selectively kills ABCB1-positive colorectal cancer cells. | ||||
| GC78967 | ELTLGEFLKL | 303068-29-3 | >99.00% | |
ELTLGEFLKL is a survivin peptide. | ||||
| GC79111 | CK2-TN03 | 313226-24-3 | >98.00% | |
CK2-TN03 is an ATP-competitive casein kinase 2 ( CK2 ) inhibitor, with an IC 50 of 165 nM and a K i of 20 nM. | ||||
| GC80875 | PROTAC survivin degrader-1 | 3079079-69-6 | >98% | |
PROTAC survivin degrader-1 is an orally active, CNS-penetrant survivin -targeting PROTAC. | ||||
| GC81531 | PBX-7016 | 3003834-34-9 | >98.00% | |
PBX-7016 is a DNA topoisomerase I inhibitor and DDX5 degrader. | ||||
