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N-(4-Fluorophenyl)-4-piperidinecarboxamide+hydrochloride
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N-(4-Fluorophenyl)-4-piperidinecarboxamide+hydrochloride
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 046436-1G , MDL Number: MFCD10758060
Catalog Number:
(TCF0302-025G)
Supplier:
TCI America
Description:
CAS Number: 351-28-0
MDL Number: MFCD00017917 Molecular Formula: C8H8FNO Molecular Weight: 153.16 Purity/Analysis Method: >96.0% (N) Form: Crystal Melting point (°C): 88
Supplier:
AMBEED, INC
Description:
Elvitegravir 98%
Catalog Number:
(89157-986)
Supplier:
Enzo Life Sciences
Description:
Cell permeable, potent and selective p38 MAP kinase inhibitor (IC50=30 nM). Inhibits p38α and ß, but not γ and δ isoforms. Does not inhibit ERK2 or other members of the MAP kinase family or their upstream activators. A useful tool for dissecting the role of p38 in signaling pathways. Induces apoptosis.
Catalog Number:
(TCC1638-025G)
Supplier:
TCI America
Description:
CAS Number: 56456-50-9
MDL Number: MFCD00004608 Molecular Formula: C7H6ClFO Molecular Weight: 160.57 Purity/Analysis Method: >97.0% (GC) Form: Crystal Melting point (°C): 43 Flash Point (°C): 110
Supplier:
TCI America
Description:
CAS Number: 347-93-3
MDL Number: MFCD00000991 Molecular Formula: C9H8ClFO Molecular Weight: 186.61 Purity/Analysis Method: >96.0% (GC) Form: Crystal Boiling point (°C): 103 Melting point (°C): 47 Flash Point (°C): 92
Supplier:
Thermo Scientific Chemicals
Description:
1g CAS: 874289-39-1, MDL: MFCD08436055
Catalog Number:
(76002-024)
Supplier:
Enzo Life Sciences
Description:
Necroptosis inhibitor
Supplier:
BeanTown Chemical
Description:
CAS: 75279-56-0; MDL No: MFCD00236029
UN No: UN3439; Haz Class: 6.1; Packing Group: II
Crystalline/Powder; Molecular Formula: C8H5ClFN ; MW: 169.59
Catalog Number:
(TCB2721-25G)
Supplier:
TCI America
Description:
CAS Number: 1009-22-9
Molecular Formula: C8H7BrFNO Molecular Weight: 232.05 Purity/Analysis Method: >98.0% (GC) Form: Crystal Melting point (°C): 118
Supplier:
Adipogen
Description:
The p38 mitogen-activated protein kinase (MAPK) signaling pathway is activated by numerous inflammatory mediators and environmental stresses. SB-242235 is a potent and moderately selective p38 MAP kinase inhibitor that may be an effective therapy for cytokine-mediated diseases such as autoimmune or inflammatory diseases. SB-242235 exhibits good oral availability in preclinical studies and has micromolar or submicomolar in vivo IC(50) values. However it is clear from studies examining SB-242235 effects on metabolism, for instance in chondrocytes and human cartilage that SB-242235 effects can be pleiotropic between species and that care must be taken when studying the interactions of multi-target inhibitors such as SB-242235.
Supplier:
Enzo Life Sciences
Description:
Inhibits cholesterol biosynthesis at the level of 2,3-oxidosqualene cyclase (OSC). Blocks OSC and cholesterol synthesis in HepG2 cells in the nanomolar range. A novel lipid lowering agent.
Supplier:
AVANTOR PERFORMANCE MATERIALS US
Description:
L-Arginine Hydrochloride, Multi-Compendial
Catalog Number:
(10118-204)
Catalog Number:
(TCF0524-25G)
Supplier:
TCI America
Description:
CAS Number: 399-31-5
Molecular Formula: C8H8FNO Molecular Weight: 153.16 Purity/Analysis Method: >98.0% (GC) Form: Crystal Boiling point (°C): 142 Melting point (°C): 78
Supplier:
AMBEED, INC
Description:
(R)-5-((1-Acryloylpyrrolidin-3-yl)oxy)-6-ethyl-3-((4-(4-(4-methylpiperazin-1-yl)piperidin-1-yl)phenyl)amino)pyrazine-2-carboxamide, Purity: 98%, CAS Number: 1448232-80-1, Appearance: White to yellow powder or crystals, Storage: Sealed in dry, Store in freezer, under -20 C, Size: 1mg
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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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