2,3-Bis(amino((2-aminophenyl)thio)methylene)succinonitrile+compou
Your search request has been modified to limit number of results. Your search was - 2,3-Bis(amino((2-aminophenyl)thio)methylene)succinonitrile+compound+with+ethanol+(1:1) |
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Supplier:
APOLLO SCIENTIFIC
Description:
EDC (N-(3-Dimethylaminopropyl)-N'-ethylcarbodiimide) 98%
Supplier:
TCI America
Description:
P-Xylylenediphosphonic Acid, Purity: >97.0%(HPLC)(T), Cas number: 4546-06-9, Molecular Formula: C8H12O6P2, Molecular Weight: 266.13, Appearance: White - Slightly pale yellow solid crystal powder, Size: 1G
Supplier:
BeanTown Chemical
Description:
CAS: 122235-70-5; MDL No: MFCD00235897
Powder; Molecular Formula: C23H26N2O6; MW: 426.46
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 042542-1G , MDL Number: MFCD00663856
Supplier:
AMBEED, INC
Description:
2-(Pyridin-3-yl)aniline, Purity: 95%, CAS Number: 177202-83-4, Appearance: Solid or liquid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 1g
Catalog Number:
(76010-102)
Supplier:
Prosci
Description:
Histone deacetylase (HDAC) and histone acetyltransferase (HAT) are enzymes that regulate transcription by selectively deacetylating or acetylating the eta-amino groups of lysines located near the amino termini of core histone proteins (1). Eight members of HDAC family have been identified in the past several years (2,3). These HDAC family members are divided into two classes, I and II. Class I of the HDAC family comprises four members, HDAC-1, 2, 3, and 8, each of which contains a deacetylase domain exhibiting from 45 to 93% identity in amino acid sequence. Class II of the HDAC family comprises HDAC-4, 5, 6, and 7, the molecular weights of which are all about two-fold larger than those of the class I members, and the deacetylase domains are present within the C-terminal regions, except that HDAC-6 contains two copies of the domain, one within each of the N-terminal and C-terminal regions. Human HDAC-1, 2 and 3 were expressed in various tissues, but the others (HDAC-4, 5, 6, and 7) showed tissue-specific expression patterns (3). These results suggested that each member of the HDAC family exhibits a different, individual substrate specificity and function in vivo. HDAC8 interacts with PEPB2-MYH11, a fusion protein consisting of the 165 N-terminal residues of CBF-beta (PEPB2) with the tail region of MYH11 produced by the inversion Inv(16)(p13q22), a translocation associated with acute myeloid leukemia of M4EO subtype. The PEPB2-MYH1 fusion protein also interacts with RUNX1, a well known transcriptional regulator, suggesting that the interaction with HDAC8 may participate to convert RUNX1 into a constitutive transcriptional repressor.
Catalog Number:
(75835-340)
Supplier:
Restek
Description:
11 components
Supplier:
AMBEED, INC
Description:
2-((5-Nitrofuran-2-yl)methylene)hydrazinecarboxamide, Purity: 98+%, CAS Number: 59-87-0, Appearance: Form: Crystal - Powder / Colour: Pale yellow - Deep yellow, Storage: Keep in dark place, Sealed in dry, 2-8C, Size: 1G
Supplier:
TCI America
Description:
O-Xylylenediphosphonic Acid, Purity: >97.0%(HPLC)(T), Cas number: 42104-58-5, Molecular Formula: C8H12O6P2, Molecular Weight: 266.13, Appearance: Very pale yellow - Pale reddish yellow solid crystal powder, Size: 1G
Catalog Number:
(TS32072-0075)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Dichloromethane-[Dâ‚‚] 99.8 atom % D for NMR spectroscopy
Supplier:
Adipogen
Description:
PIK-75 is a PI3K inhibitor displaying selectivity for the p110alpha isoform (IC(50) of 6nM). PIK-75 blocks the phosphorylation of PKB induced by insulin.
Supplier:
Thermo Scientific Chemicals
Description:
PYR-41 is a cell permeable inhibitor of Ubiquitin activating enzyme (E1) with little or no activity against E3, E2, or caspase enzymatic activity.
Catalog Number:
(75835-342)
Supplier:
Restek
Description:
Calibration standard Food Industry FAME Mix, 37 components, Concentration: 30 mg/mL total in methylene chloride, Volume: 1 mL/ampule
Catalog Number:
(95062-676)
Supplier:
MilliporeSigma
Description:
STAT5 inhibitor is a cell-permeable compound that selectively targets the SH2 domain of STAT5 (IC50 = 47 µM against STAT5b SH2 domain EPO peptide binding activity).
Supplier:
Adipogen
Description:
VX745 is a selective inhibitor of p38alpha with an IC(50) of 10nM.
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