Tocris/PRT 4165/5047/50/50 mg
克隆和表達
商品編號
5047/50
品牌
Tocris
公司
Bio-Techne Corporation
公司分類(lèi)
Ligases
Size
50 mg
商品信息
Description:
Inhibitor of Bmi1/Ring1A; blocks histone H2A ubiquitination
Chemical Name:
2-(3-Pyridinylmethylene)-1
H
-Indene-1,3(2
H
)-dione
Purity:
≥99% (HPLC)
BIOLOG
ical Activity
Technical Data
Solubility
Calculators
Datasheets
References
BIOLOG
ical Activity
Inhibitor of Bmi1/Ring1A, subunits of the polycomb repressive complex 1 (PRC1); inhibits self-ubiquitination (IC
50
= 3.9
μ
M) but does not increase cellular levels of either subunit. Prevents Bmi1/Ring1A-mediated ubiquitination and drug-induced degradation of topoisomerase 2
α
(Top2
α
). Also shown to inhibit the
in vitro
E3 ubiquitin ligase activity of RNF2 and a Bmi1/RNF2 complex, inhibiting H2A/H2AX ubiquitination. Blocks polycomb repressor complex (PRC) 1-mediated histone H2A ubiquitination
in vitro
and
in vivo
.
Compound Libraries
PRT 4165 is also offered as part of the
Tocris
creen Plus and
Tocris
creen Epigenetics Toolbox. Find out more about compound libraries available from
Tocris
.
Technical Data
M. Wt
235.24
Formula
C
15
H
9
NO
2
Storage
Store at +4°C
Purity
≥99% (HPLC)
CAS Number
31083-55-3
PubChem ID
207893
InChI Key
OMHZFEWYVFWVLI-UHFFFAOYSA-N
Smiles
O=C(C2=CC=CC=C2C3=O)/C3=CC1=CC=CN=C1
The technical data provided above is for guidance only. For batch specific data refer to the Certificate of Analysis.
All
Tocris
products are intended for laboratory research use only.
Solubility Data
Solvent
Max Conc. mg/mL
Max Conc. mM
Solubility
1eq. HCl
1.18
5mM with gentle warming
DMSO
23.52
100
ethanol
2.35
10mM with gentle warming
Preparing Stock Solutions
The following data is based on the
product
molecular weight
235.24
. Batch specific molecular weights may vary from batch to batch due to solvent of hydration, which will affect the solvent volumes required to prepare stock solutions.
Concentration / Solvent Volume / Mass
1 mg
5 mg
10 mg
1 mM
4.25 mL
21.25 mL
42.51 mL
5 mM
0.85 mL
4.25 mL
8.5 mL
10 mM
0.43 mL
2.13 mL
4.25 mL
50 mM
0.09 mL
0.43 mL
0.85 mL
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Product Datasheets
Certificate of Analysis / Product Datasheet
Safety Datasheet
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References
References are publications that support the products'
BIOLOG
ical activity.
Alchanati
et al
(2009) The E3 ubiquitin-ligase Bmi1/Ring1A controls the proteasomal degradation of Top2
α
cleavage complex - a potentially new drug target. PLoS One
4
e8104 PMID: 19956605
Ismail
et al
(2013) A small molecule inhibitor of polycomb repressive complex 1 inhibits ubiquitin signaling at DNA double-strand breaks. J.Biol.Chem.
288
26944 PMID: 23902761
Keywords: PRT 4165, supplier, PRT4165, E3, ubiquitin, ligase, inhibitors, inhibits, Bmi1, Ring1A, ubiquitination, ubiquitylation, topoisomerase, 2a, Top2a, Top2alpha, Top2α, polycomb, repressive, complex, 1, PRC1, RNF2, Bmi1/RNF2, Ubiquitin, E3, Ligases, Ubiquitin, E3, Ligases,
Tocris
Bioscience
產(chǎn)品貨號:3428.0