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Catalog No. Product Name Application Product Information
A15472

Finafloxacin hydrochloride

-
Finafloxacin hydrochloride is a fluoroquinolone compound.
A15502

MCI-225

NA reuptake inhibitor
MCI-225 is a selective NA reuptake inhibitor with 5-HT3 receptor antagonism.
A11534

Pentostatin

Adenosine deaminase inhibitor
Pentostatin is an irreversible inhibitor of adenosine deaminase (Ki = 2.5 pM).
A15774

ISX-9

Neurogenic Modulator
ISX-9 is a small molecule inducer of adult neural stem cell differentiation.
A15770

Ursodeoxycholic acid

-
Ursodeoxycholic acid (UDCS) is a cell protectant used extensively to mitigate hepatic and biliary diseases.
A14444

SAR191801

hPGDS inhibitor
SAR191801 is a hPGDS inhibitor ,with IC50 of 12 nM in the Fluorescence Polarization Assay or the EIA assay.
A15223

Retinyl glucoside

-
Retinyl glucoside is a naturally occurring and biologically active metabolites of vitamin A, which are found in fish and mammals.
A15204

Pamabrom

-
Pamabron is a common over-the-counter diuretic used for relief of menstrual-associated symptoms.
A15203

Pafuramidine

-
Pafuramidine is an orally bioavailable prodrug of furamidine, which has clinical activity against Pneumocystis pneumonia.
A14966

(Z)-2-decenoic acid

-
(Z)-2-decenoic acid is an unsaturated short chain fatty acid that is secreted by P. aeruginosa and induces a disp .
A14982

9-Dihydro-13-acetylbaccatin III

-
9-Dihydro-13-acetylbaccatin III (9-DHAB III) is an intermediate for taxol analog preparations.
A15020

Benfotiamine

-
Benfotiamine is a synthetic S-acyl derivative of thiamine (vitamin B1), an antioxidant dietary supplement.
A15027

BMX-IN-1

BMX kinase inhibitor
BMX-IN-1 is a highly selective and potent irreversible inhibitor which target the cysteine residue in the BMX ATP binding domain.
A15034

Calcium-Sensing Receptor Antagonists I

Calcium-Sensing Receptor Antagonist
Calcium-Sensing Receptor Antagonists I is an antagonist of calcium-sensing parathyroid hormone receptors.
A15043

c-FMS inhibitor

FMS inhibitor
c-FMS inhibitor is a potent, orally active and small-molecule inhibitor of FMS kinase with IC50 value of 0.8 nM.
A15052

Cot inhibitor-2

COT/Tpl2 inhibitor
Cot inhibitor-2 is a COT/Tpl2 inhibitor.
A15063

Deferasirox Fe3+ chelate

-
Deferasirox Fe3+ chelate is a rationally-designed oral iron chelator; its main use is to reduce chronic iron overload in patients who are receiving long-term blood transfusions for conditions such as beta-thalassemia and other chronic anemias.
A15074

EBE-A22

-
EBE-A22 is a derivative of PD 153035 which can inhibit ErbB-1-phosphorylation, whereas EBE-A22 is inactive.
A15079

EMD638683

SGK inhibitor
EMD638683 is a potent inhibitor of SGK1 with an IC50 value of 3 uM.
A15085

Etimizol

-
Etimizol was shown to relieve amnesia effectively in the origin of which there is the hypoxic component (hypobaric hypoxia, actinomycin D, mechanical injury of the brain).
A15155

MB05032

GNG inhibitor
MB05032 is a special and efficacious GNG inhibitor targeted the AMP binding site of fructose 1,6-bisphosphatase (FBPase) with an IC50 value of 16 nM.
A15173 SALE

MPTP hydrochloride

DA neurotoxin
MPTP hydrochloride induced reduction in the DOPAC HVA/dopamine (DA) ratio and increase in striatal ascorbate (AS) oxidation in rats.
A15176

N3PT

TK inhibitor
N3PT is a potent and selective transketolase(TK) inhibitor (IC50= 22 nM for Apo-TK) both in vitro and in vivo.
A15179

NB-598 hydrochloride

SE inhibitor
NB-598 is a potent competitive inhibitor of squalene epoxidase (SE). NB-598 suppresses triglyceride biosynthesis through the farnesol pathway.
A15180 SALE

NB-598 Maleate

SE inhibitor
NB-598 is a potent competitive inhibitor of squalene epoxidase (SE). NB-598 suppresses triglyceride biosynthesis through the farnesol pathway.
A15181

NB-598 Maleate salt

SE inhibitor
NB-598 is a potent competitive inhibitor of squalene epoxidase (SE). NB-598 suppresses triglyceride biosynthesis through the farnesol pathway.
A15433

Cyclosporin B

Immunomodulators
Cyclosporin B is an immunosuppressant that has revolutionized organ transplantation through its use in the prevention of graft rejection.
A15435

Cyclosporin H

TPA/PMA inhibitor
Cyclosporin H is a TPA/PMA inhibitor and a selective inhibitor of formyl peptide receptors (Ki = 0.1 uM).
A15445

K-7174

Cell adhesion inhibitor
K-7174 is a novel cell adhesion inhibitor; inhibits the expression of vascular cell adhesion molecule-1 (VCAM-1) induced by either IL-1beta or TNF-alpha.
A15881

BEC HCl

arginase inhibitor
BEC HCl is a slow-binding, and competitive arginase inhibitor with Ki of 0.31 μM (pH7.5) and 0.4-0.6 μM for Arginase II and rat Arginase I, respectively.
A15897

Coelenterazine

luminescent enzyme substrate
Coelenterazine is a luminescent enzyme substrate, used for monitoring reporter genes in BRET, ELISA and HTS techniques.
A12901

Disodium (R)-2-Hydroxyglutarate

-
Disodium (R)-2-Hydroxyglutarate is a competitive inhibitor of ??-ketoglutarate-dependent dioxygenases with Ki of 0.628 mM.
A13789

D-Luciferin

Bioluminescent substrate
D-Luciferin is a popular bioluminescent substrate of luciferase in the presence of ATP, used in luciferase-based bioluminescence imaging and cell-based high-throughput screening applications.
A15861

2,2,2-Tribromoethanol

-
2,2,2-Tribromoethanol is an organic compound used to anesthetize mice.
A15862

CB1954

-
CB1954 is a anticancer prodrug that is converted in the presence of the enzyme NQO2 and co-substrate caricotamide ( EP-0152R) (EP) into a potent cytotoxic bifunctional alkylating agent.It can be activated by NAD(P)H quinone oxidoreductase 2.
A13885

LHW090-A7

NEP inhibitor
LHW090-A7 is an inhibitor of neutral endopeptidase (NEP), an enzyme responsible for the metabolic inactivation of enkephalins.
A15828

CPI-268456

-
N/A
A15834

Picaridin

-
Picaridin is an insect repellant that acts on certain olfactory receptor cell types to reduce the activating or attracting effect of odor sources.
A15852

DAA-1106

PBR agonist
DAA-1106 is a potent and selective ligand for peripheral benzodiazepine receptor (PBR), as a potent and selective agonist at the peripheral benzodiazepine receptor.
A11475

Ko-143

BCRP inhibitor
Ko 143 is potent and selective inhibitor of breast cancer resistance protein multidrug transporter (BCRP) with an EC90 value of 26 nM.
A12240

Butylphthalide

-
Butylphthalide is an antioxidant and one of the chemical constituents in celery oil, along with sedanolide, which is primarily responsible for the aroma and taste of celery.
A15938

Alanosine (SDX-102)

-
Alanosine is an amino acid analogue and antibiotic derived from the bacterium Streptomyces alanosinicus with antimetabolite and potential antineoplastic activities.
A15949

GABOB (beta-hydroxy-GABA)

-
GABOB is an anticonvulsant which is used for the treatment of epilepsy in Europe, Japan, and Mexico.
A15951

Iloprost

-
Iloprost is a drug used to treat pulmonary arterial hypertension (PAH), scleroderma, Raynaud's phenomenon and other diseases in which the blood vessels are constricted and blood can't flow to the tissues.
A15952

Isosorbide Mononitrate

-
Isosorbide Mononitrate is a drug used principally in the treatment of angina pectoris and acts by dilating the blood vessels so as to reduce the blood pressure.
A15953 SALE

J147

neuroprotective and neurotrophic compound
J147 is a potent neuroprotective and neurotrophic compound. J147 protects against neurotoxicity in cortical neurons in vitro (EC50 = 25 - 200 nM).
A15879

LTX-315

Oncolytic peptide
LTX-315 is the oncolytic peptide that kills cancer cells through Bax/Bak-regulated mitochondrial membrane permeabilization.
A15932 SALE

3PO

PFKFB3 inhibitor
3PO is a PFKFB3 (6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase) inhibitor.
A15926

Brevianamide F

-
Brevianamide F belongs to a class of naturally occurring 2,5-diketopiperazines.
A15446

K-7174 2HCl

Cell adhesion inhibitor
K-7174 dihydrochloride is a novel cell adhesion inhibitor; inhibits the expression of vascular cell adhesion molecule-1 (VCAM-1) induced by either IL-1beta or TNF-alpha.

Items 251 to 300 of 728 total

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