5-Bromobenzo[1,3]dioxole-4-carboxylic+acid
Supplier:
Thermo Scientific Chemicals
Description:
25g CAS: 330641-16-2, MDL: MFCD04973270
Supplier:
AMBEED, INC
Description:
RP-54745, Purity: 98%, CAS Number: 135330-08-4, Appearance: Solid, Storage: Inert atmosphere, 2-8C, Size: 5MG
Supplier:
ALADDIN SCIENTIFIC
Description:
Asenapine maleate is a 5-HT (1A, 1B, 2A, 2B, 2C, 5A, 6, 7) and D2 antagonist with Ki values of 0.03-4.0 nM, 1.3nM, respectively, and an antipsychotic.Asenapine maleate is a serotonin 5-HT and dopamine D2 receptor antagonist. Asenapine maleate can be used to treat schizophrenia and bipolar mania.
Supplier:
MORAVEK BIOCHEMICALS MS
Description:
Efavirenz ≥98% (by HPLC), MORpure™
Supplier:
MP Biomedicals
Description:
Storage: Store at -20 °C. Store Desiccated. Store Under Nitrogen. Protect from light.
5-Bromo-4-chloro-3-indolyl β-D-galactopyranoside, commonly known as X−Gal, is a histochemical substrate for β−galactosidase. 5-Bromo-4-Chloro-3-Indolyl-β-D-Galactopyranoside is used as indigogenic substrate for β-galactosidase, for detection of β-galactosidase-positive clones, and the identification of lac and bacterial colonies or phage plaques. It is the substrate of choice for blue-white selection of recombinant bacterial colonies with the lac+ genotype. X−Gal is cleaved by β−galactosidase to yield an insoluble blue precipitate. X−Gal is particularly useful in molecular biology applications to detect the activity of β−galactosidase which is frequently used as a reporter gene. In cloning, X−Gal is used to detect insertion of foreign DNA into the lacZ region of plasmid DNA using α-complementation which is based on vectors such as the pUC and the M13mp series that carry a fragment of the β-galactosidase gene encoding an α-fragment of β-galactosidase.
Supplier:
AMBEED, INC
Description:
2-(3-((4-(4-Methoxyphenyl)-5-(pyridin-4-yl)-4H-1,2,4-triazol-3-yl)thio)propyl)-1H-benzo[de]isoquinoline-1,3(2H)-dione, Purity: 98%, CAS Number: 838818-26-1, Appearance: Form: solid, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 50mg
Supplier:
AMBEED, INC
Description:
4-Chloro-7-azaindole 98%, Ambeed.Inc
Supplier:
AMBEED, INC
Description:
Dichlorobis[3-(diphenylphosphino-KP)-1-propanamine-KN]ruthenium, Purity: 98%, CAS Number: 911128-25-1, Appearance: Solid, Storage: Keep in dark place, Inert atmosphere, 2-8 C, Size: 100mg
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
O-(6-Chlorobenzotriazol-1-yl)-N,N,N',N'-tetramethyluronium Hexafluorophosphate 98%
Supplier:
Enzo Life Sciences
Description:
Selective TNF-α inhibitor.
Catalog Number:
(TCA1650-5G)
Supplier:
TCI America
Description:
CAS Number: 1912-24-9
MDL Number: MFCD00041810 Molecular Formula: C8H14ClN5 Molecular Weight: 215.69 Purity/Analysis Method: >97.0% (GC,T) Form: Crystal Melting point (°C): 177
Supplier:
AMBEED, INC
Description:
4-Chloro-N-(5-(4-fluorophenyl)-1,3,4-oxadiazol-2-yl)benzamide, Purity: 98+%, CAS Number: 865285-29-6, Appearance: White to beige powder or crystals, Storage: Sealed in dry, 2-8C, Size: 5MG
Supplier:
AMBEED, INC
Description:
7-Chloroindole, Purity: 98%, CAS number: 53924-05-3, Appearance: Form: Crystal - Powder / Colour: White - Yellow, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 25G
Supplier:
AMBEED, INC
Description:
5-Amino-6-chloropyrimidin-4(1H)-one, Purity: 95%, CAS number: 3137-60-8, Appearance: Off-white to light yellow powder or crystals, Storage: Keep in dark place, Inert atmosphere, 2-8C, Size: 100MG
Supplier:
TCI America
Description:
CAS Number: 73616-27-0
MDL Number: MFCD08063809 Molecular Formula: C5H9N3O Molecular Weight: 127.15 Purity/Analysis Method: >99.0% (GC) Form: Crystal Boiling point (°C): 140 Melting point (°C): 108
Supplier:
Adipogen
Description:
pan-Akt inhibitor targeting Akt1, 2, 3 with IC50 values of 2, 13 and 9 nM, respectively. Inhibits AMPK, DAPK3, PAK4, 5 and 6, as well as members of the AGC kinase family including PKA, PrkX and PKC isoforms (IC50 <lt/> 100 nM). Occupies the ATP binding pocket of the kinase domain and competes with ATP. Anti-cancer compound both in vitro and in vivo. Blocks the phosphorylation of downstream targets of ATK in a dose-dependent manner, which leads to antiproliferative and apoptotic effects in tumor cell lines. Induces hyperglycemia related to peripheral insulin resistance, increased gluconeogenesis, and/or hepatic glycogenolysis.
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