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(R)-Methyl+2-amino-3-methoxypropanoate+hydrochloride
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(R)-Methyl+2-amino-3-methoxypropanoate+hydrochloride
Catalog Number:
(101934-124)
Supplier:
Matrix Scientific
Description:
MF=C17H21Clf2N2O2S MW=390.88 ,250Mg
Catalog Number:
(101934-332)
Supplier:
Matrix Scientific
Description:
MF=C18H24Cl2N2O2S MW=403.37 ,250Mg
Supplier:
TCI America
Description:
CAS Number: 6018-56-0
MDL Number: MFCD00070606 Molecular Formula: C3H8N2O2 Molecular Weight: 140.57 Purity/Analysis Method: >98.0% (N) Form: Crystal Melting point (°C): 240 Specific rotation [a]20/D: -23 deg (C=2, 1mol/L HCl)
Catalog Number:
(77981-581)
Supplier:
LGC STANDARDS
Description:
3-Deschloro-4-chloro Bupropion Hydrochloride, TRC, LGC Standards
Supplier:
Bachem Americas
Description:
Sequence: Bz-Arg-pNA · HCl
Supplier:
TCI America
Description:
CAS Number: 69320-89-4
MDL Number: MFCD00058015 Molecular Formula: C10H21NO2 Molecular Weight: 223.74 Purity/Analysis Method: >98.0% (N,T) Form: Crystal Melting point (°C): 160 Specific rotation [a]20/D: 15 deg (C=1, H2O)
Catalog Number:
(77981-649)
Supplier:
LGC STANDARDS
Description:
Desethyl Amiodarone-d4 Hydrochloride, TRC, LGC Standards
Supplier:
TCI America
Description:
CAS Number: 41100-52-1
MDL Number: MFCD00214336 Molecular Formula: C12H21N Molecular Weight: 215.77 Purity/Analysis Method: >98.0% (N,T) Form: Crystal Melting point (°C): 292
Supplier:
AMBEED, INC
Description:
1,1,1-Trifluoropropan-2-amine hydrochloride, Purity: 98%, CAS Number: 2968-32-3, Appearance: White to Yellow Solid, Storage: Inert atmosphere, Room Temperature, Size: 5G
Supplier:
Thermo Scientific Chemicals
Description:
L-Phenylalaninamide hydrochloride, 97%
Catalog Number:
(101934-344)
Supplier:
Matrix Scientific
Description:
MF=C14H20Cln5O MW=309.80 ,500Mg
Supplier:
AMBEED, INC
Description:
Neutral red 98% BS
Supplier:
AMBEED, INC
Description:
H-Val-OBzl·HCl 97%
Catalog Number:
(77696-349)
Supplier:
LGC STANDARDS
Description:
Glufosinate hydrochloride D3 (methyl D3), Dr. Ehrenstorfer, LGC Standards
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.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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