4-Chloro-1-ethyl-1H-pyrazole
Catalog Number:
(E-2670.0025BA)
Supplier:
Bachem Americas
Description:
Sequence: H-Glu(OEt)-OEt · HCl
Catalog Number:
(77697-662)
Supplier:
LGC STANDARDS
Description:
Osmium Standard: Os @ 10 µg/mL in 5% HCl, VHG, LGC Standards
Supplier:
TCI America
Description:
CAS Number: 333-93-7
MDL Number: MFCD00012526 Molecular Formula: C4H12N2 Molecular Weight: 161.07 Purity/Analysis Method: >98.0% (T) Form: Crystal
Supplier:
AMBEED, INC
Description:
4-(Trifluoromethyl)benzamidine hydrochloride 97%
Supplier:
MP Biomedicals
Description:
Vancomycin inhibits bacterial mucopeptide biosynthesis
Supplier:
TLC PHARMACEUTICAL STANDARD LTD
Description:
Pharmaceutical Standards, Oseltamivir EP Impurity A HCl
Supplier:
TLC PHARMACEUTICAL STANDARD LTD
Description:
Pharmaceutical Standards, Brimonidine EP Impurity G HCl
Supplier:
TLC PHARMACEUTICAL STANDARD LTD
Description:
Pharmaceutical Standards, Cyclophosphamide Impurity 28 HCl
Catalog Number:
(103256-990)
Supplier:
HCL Label
Description:
HCL's high-quality labels meet all necessary safety and OSHA requirements, as well as being a great value for their size and quantities.
Supplier:
TCI America
Description:
CAS Number: 554-68-7
MDL Number: MFCD00012500 Molecular Formula: C6H15N Molecular Weight: 137.65 Purity/Analysis Method: >98.5% (T) Form: Crystal Color: White Melting point (°C): 258
Supplier:
AMBEED, INC
Description:
Moroxydine hydrochloride 98%
Supplier:
TLC PHARMACEUTICAL STANDARD LTD
Description:
Pharmaceutical Standards, Labetalol EP Impurity A HCl (Labetalol USP Related Compound A) (Mixture of Diastereomers)
Supplier:
Adipogen
Description:
CC-401 is a competitive inhibitor of the ATP binding site in the active, phosphorylated, form of JNK. This prevents JNK from phosphorylating its various target molecules, including the amino terminus of c-Jun. It is a potent inhibitor of all three forms of JNK (Ki of 25-50 nM), and has at least 40-fold selectivity for JNK compared with other related kinases, including: p38, ERK, IKK2, PKC, Lck, and ZAP70. CC-401 acts to inhibit JNK signaling by competitive binding to the adenosine triphosphate-binding site in the active, phosphorylated, form of JNK, resulting in inhibition of the phosphorylation of JNK targets, such as the amino-terminal activation domain of the transcription factor, c-Jun. In cell-based assays, 1-5 muM CC-401 provides specific JNK inhibition.
Catalog Number:
(TCB3379-5G)
Supplier:
TCI America
Description:
[for Biochemical Research]
CAS Number: 1670-14-0 MDL Number: MFCD00013025 Molecular Formula: C7H8N2 Molecular Weight: 156.61 Purity/Analysis Method: >95.0% (N,T) Form: Crystal Melting point (°C): 171
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