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Supplier:
AMBEED, INC
Description:
(R)-9-(4-(1-(Dimethylamino)propan-2-yl)phenyl)-8-hydroxy-6-methylthieno[2,3-c]quinolin-4(5H)-one hydrochloride, Purity: 98%, CAS Number: 1338545-07-5, Appearance: White to off-white solid, Storage: Sealed in dry, Store in freezer, under -20 C, Size: 50mg
Catalog Number:
(IC15667625)
Supplier:
MP Biomedicals
Description:
Strychnine is an poisonous alkaloid extract obtained from the dried ripe seeds of Strychnos nux vomica, a small tree of the East Indies. It is obtained as a white crystalline substance, having a very bitter acrid taste, and is used in research as a powerful neurostimulant.
Catalog Number:
(77697-406)
Supplier:
LGC STANDARDS
Description:
Methcathinone Hydrochloride (2-Methylamino-1-phenylpropan-1-one Hydrochloride), Mikromol, LGC Standards
Catalog Number:
(76482-336)
Supplier:
AAT BIOQUEST INC
Description:
MCLA has been used to assess superoxide formation in a variety of conditions, including neutrophil and macrophage activation, cultured cells and vascular tissue.
Supplier:
TCI America
Description:
[for Biochemical Research]
CAS Number: 22198-72-7 MDL Number: MFCD00042012 Molecular Formula: C11H13N3O Molecular Weight: 239.70 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal
Supplier:
MP Biomedicals
Description:
Pyridoxine Hydrochloride is one of the vitamins of the B6 complex; present in many foodstuffs (yeast, liver and cereals).
Catalog Number:
(TCA5309-010MG)
Supplier:
TCI America
Description:
[Chemiluminescence Reagent]
CAS Number: 128322-44-1 MDL Number: MFCD00144728 Molecular Formula: C14H13N3O2 Molecular Weight: 291.74 Purity/Analysis Method: >98.0% (HPLC) Form: Crystal Storage Temperature: 0-10°C
Supplier:
MP Biomedicals
Description:
Naloxine is specific and competitive opiate antagonist at mu, kappa, delta and sigma receptors; it blocks the action of sigma-agonists at opioid sites. It displaces morphine and other opiate agonists from the opiate receptor. It is more potent than Nalorphine and is also an effective antagonist for mixed agonist-antagonist drugs such as pentazorcine. Naloxone has no respiratory depressant activity.
Supplier:
MP Biomedicals
Description:
Thiamine (Vitamin B1) is one of the essential vitamins and is required for carbohydrate metabolism.
Supplier:
AMBEED, INC
Description:
1-Benzyl-3-pyrrolidinone 97%
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 045302-1G , MDL Number: MFCD08056659
Catalog Number:
(101843-658)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 037557-500MG , MDL Number: MFCD00158810
Supplier:
ALADDIN SCIENTIFIC
Description:
5-Amino-8-hydroxyquinoline dihydrochloride was used in synthesis of: . 5-acetamido-8-hydroxyquinoline hydrochloride . 5-(p-tolylsulfonylimino)quinolin-8-one . 5,8-quinolinesemiquinone via ferric chloride oxidation
Catalog Number:
(TCD2400-25G)
Supplier:
TCI America
Description:
CAS Number: 879-72-1
MDL Number: MFCD00012481 Molecular Formula: C11H15NO Molecular Weight: 213.71 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 153
Supplier:
Adipogen
Description:
AT7519 is a potent inhibitor of several CDK family members. AT7519 showed potent antiproliferative activity (40-940nM) in a panel of human tumor cell lines, and the mechanism of action was shown here to be consistent with the inhibition of CDK1 and CDK2 in solid tumor cell lines. AT7519 caused cell cycle arrest followed by apoptosis in human tumor cells and inhibited tumor growth in human tumor xenograft models. Tumor regression was observed following twice daily dosing of AT7519 in the HCT116 and HT29 colon cancer xenograft models. Also it has been shown that the biological effects are linked to inhibition of CDKs in vivo and that AT7519 induces tumor cell apoptosis in these xenograft models. Moreover, AT7519 has an attractive biological profile and is well tolerated and effective making it a more plausible candidate for clinical development than previously available CDK inhibitors. In in vitro kinase assays AT7519 showed nanomolar levels of activity from <lt/>10 to 2400 for cyclins; only one other non-cyclin related kinase was inhibited at levels below 10µM (GSK3beta, 89nM), all others tested had IC(50)'s of greater than 10,000nM.
Supplier:
ALADDIN SCIENTIFIC
Description:
2 arm PEG derivatives have two PEG branches with one or two functional groups that can be used to modify proteins, peptides and other materials via their functional groups. PEGylation can increase solubility and stability and reduce immunogenicity of peptides and proteins. It can also suppress the non-specific binding of charged molecules to the modified surfaces. .
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 is still displayed and you need assistance, please call us at 1-800-932-5000.
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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