You Searched For: Piperazine+dihydrochloride


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Catalog Number: (CA80055-236)
Supplier: MilliporeSigma
Description: Principal alkaloid of ipecac, isolated from the ground roots of Uragoga ipecacuanha

Supplier: Enzo Life Sciences
Description: Inhibits protein synthesis
Supplier: Enzo Life Sciences
Description: CP-31398 restores mutant p53 tumor suppressor function in vitro without affecting p53 homologs p63 and p73, and in vivo inhibiting UVB-induced skin carcinogenesis in mice. Stabilization of p53 inhibits ubiquitination without altering phosphorylation at Ser12 or Ser20 or MDM2 binding. Administration of this or similar compounds has the potential to enhance cytotoxic chemotherapy.

Supplier: TCI America
Description: CAS Number: 6055-52-3
MDL Number: MFCD00012528
Molecular Formula: C6H16N2
Molecular Weight: 189.12
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Melting point (°C): 248
Supplier: TCI America
Description: 1,4-Diazabicyclo[2.2.2]octane Dihydrochloride, Purity: >98.0%(N)(T), CAS number: 49563-87-3, Molecular Formula: C6H12N2.2HCl, Molecular Weight: 185.09, Form: Crystal - Powder, White - Almost white, Size: 1G

Supplier: MilliporeSigma
Description: 4-Hydroxy-1,3-phenylenediammonium dichloride, CAS Number: 137-09-7, for synthesis.

SDS

Supplier: Bachem Americas
Description: Sequence: H-3-Amino-Tyr-OH · 2 HCl

Supplier: TCI America
Description: CAS Number: 16523-31-2
MDL Number: MFCD00143239
Molecular Formula: C6H8N2O2
Molecular Weight: 213.06
Purity/Analysis Method: >98.0% (N,T)
Form: Crystal
Supplier: Enzo Life Sciences
Description: Inhibits Rho kinase (ROCK; Ki=0.33μM). Selective protein kinase A and G inhibitor (both Ki’s = 1.6μM). Inhibits agonist-induced activation of NADPH oxidase in human neutrophils (IC50=15μM). Inhibitor of myosin light chain kinase and Ca2+/calmodulin-dependent protein kinase II. Inhibits translocation of PKCβI, PKCβII and PKCζ. Cell permeable Ca2+ antagonist with antivasospastic properties.

Supplier: TCI America
Description: CAS Number: 103831-11-4
MDL Number: MFCD00060176
Molecular Formula: C4H10N2
Molecular Weight: 159.05
Purity/Analysis Method: >98.0% (N)
Form: Crystal
Supplier: TCI America
Description: CAS Number: 26340-89-6
MDL Number: MFCD00038948
Molecular Formula: C7H16N4O2
Molecular Weight: 261.15
Purity/Analysis Method: >98.0% (N,T)
Form: Crystal
Melting point (°C): 193
Specific rotation [a]20/D: 21 deg (C=2.5, MeOH)
Supplier: Bachem Americas
Description: Sequence: H-Phe-Arg-βNA · 2 HCl

Supplier: Enzo Life Sciences
Description: A cell permeable, highly specific, potent and ATP-competitive inhibitor of Rho kinase (ROCK) (Ki=1.6nM). Exhibits a much weaker affinity for other serine/threonine kinases (Ki=630nM for PKA, 9.27mM for PKC and 10.1mM for MLCK). More potent and selective than Y-27632. Inhibits the phosphorylation of MARCKS in cells stimulated by lysophosphatidic acid. Inhibits EP3-stimulated NO formation. Prevents fragmentation of apoptotic cells. Relieves neuropathic pain.

Catalog Number: (TCM1995-1G)
Supplier: TCI America
Description: Molecular Weight: 289.24
Purity/Analysis Method: >98.0% (T)
Form: Crystal
Specific rotation [a]20/D: -44 deg (C=1, H2O)
Molecular Formula: C14H20N2

SDS


Supplier: VWR
Description: Biological buffers are useful for cell culture <i>in vitro</i>, enzyme assays, and some electrophoretic applications at physiological pH.
Catalog Number: (CAAAH60753-03)
Supplier: Thermo Scientific Chemicals

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