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Cat. No. Product Name Field of Application Chemical Structure
DC36201 S-(3-Carboxypropyl)-L-cysteine
S-(3-Carboxypropyl)-L-cysteine is a thioether derivative of L-cysteine.
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DC36671 Perfluorosebacic acid
Perfluorosebacic acid (Hexadecafluorosebacic acid) is a perfluoroalkanedicarboxylic acid, useful in the preparation of synthetic polymers.
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DC34461 IMB-10
IMB-10 is an alphaMbeta2 integrin modulator, inhibiting leukocyte migration and recruitment in vitro and in vivo.
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DC37941 Metildigoxin
Metildigoxin is a semisynthetic digitalis glycoside with the general properties of DIGOXIN but more rapid onset of action. Its cardiotonic action is prolonged by its demethylation to DIGOXIN in the liver. It has been used in the treatment of congestive heart failure.
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DC36686 Propyl caprate
Propyl caprate is a biochemical.
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DC37881 Alanylphenylalanine
Alanylphenylalanine may be used in physicochemical studies or to evaluate dipeptide separation technologies. It can also be used for studying cell uptake mechanisms, dipeptide metabolism or cell growth supplementation benefits.
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DC37819 Hyoscyamine hydrobromide
Hyoscyamine hydrobromide is an anticholinergic.
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DC34681 Oxamyl oxime
Oxamyl oxime is an agricultural chemical and pesticide.
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DC34173 CCT036477
CCT036477 is a selective inhibitor of wingless-type MMTV integration site family (WNT)-dependent transcription. It reduces the transcriptional activity of the T-cell factor/lymphoid enhancer factor transcription factor family at the ?-catenin level.
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DC35067 Biotin-PEG2-Mal
Biotin-PEG2-Mal is a PEG derivative containing a biotin group and a maleimide group for labeling and crosslinking cysteines and other sulfhydryls. The maleimide group reacts specifically with sulfhydryl groups (at pH 6.5-7.5) to form a stable, irreversible thioether linkage. The hydrophilic PEG spacer increases solubility in aqueous media and increases membrane impermeability of the molecules conjugated to the biotin compound. It also helps to minimize steric hindrance involved with the binding to avidin molecules.
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DC37326 Analepticon
Ethamivan, or etamivan, is a respiratory stimulant drug related to nikethamide. It has been mainly used in the treatment of barbiturate overdose and chronic obstructive pulmonary disease.
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DC34130 Succimer
Succimer is an orally active heavy metal chelator.
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DC37771 L-Cystine S
L-Cystine S,S-dioxide is a metabolite of L-Cystine.
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DC36071 Harmaline
Harmaline is a beta-carboline alkaloid isolated from seeds of PEGANUM. It is a psychoactive indole with stimulating activities achieved, in part, through inhibition of monoamine oxidases. Harmaline induces tremor in mice through the N-methyl-D-aspartate (NMDA) receptor, at which harmaline may act as an inverse agonist.
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DC36388 NSC 613948
Nybomycin is a fungal metabolite with antibacterial activity. It is active against B. subtilis, B. cereus, B. mycoides, M. smegmatis, and K. pneumoniae. Nybomycin is also active against M. tuberculosis and M. bovis.
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DC37230 N-Piperidinoethanol
N-Piperidinoethanol is a biochemical.
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DC34216 Acetyl-L-carnitine
Acetyl-L-carnitine is a stimulator of α-secretase activity and metabolism of amyloid precursor protein (APP). It has been shown to induce NF-κB-mediated upregulation of mGluR2 receptors, thereby exhibiting antidepressant, neuroprotective, analgesic, and antinociceptive activities.
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DC37498 Bitolterol mesylate
Bitolterol mesylate is a Bronchodilator.
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DC37392 Novobiocin
Novobiocin is an antibiotic compound derived from Streptomyces niveus. It has a chemical structure similar to coumarin. Novobiocin binds to DNA gyrase, and blocks adenosine triphosphatase (ATPase) activity
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DC37408 AI3-51769
Heliotrine leads to induction of apoptosis in the human hepatoma cell line HepaRG.
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DC34378 Norchlorcyclizine
Norchlorcyclizine is a partially selective NPR-B inhibitor. It also acts as an inhibitor of human tyrosyl-DNA phosphodiesterase 1 (TDP1).
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DC36140 Aica ribonucleotide
AICAR, also known as AICA riboside, is a purine precursor with antineoplastic activity. It is important in treatment of metabolic diseases such as type 2 diabetes as well as possible treatment of various cancer types.
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DC36431 (-)-Rasfonin
(-)-Rasfonin is a fungal metabolite that inhibits proliferation of mouse splenocytes induced by concanavalin A and LPS.
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DC36181 Antioxidant ZMB
Antioxidant ZMB is an antioxidant.
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DC37578 Sodium deoxycholate
Sodium deoxycholate is a bile acid formed by bacterial action from cholate. It is usually conjugated with glycine or taurine. Deoxycholic acid acts as a detergent to solubilize fats for intestinal absorption, is reabsorbed itself, and is used as a choleretic and detergent.
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DC33872 BDP FL alkyne
Alkyne derivative of BDP FL, an analog of BODIPY? FL alkyne. BDP FL is a borondipyrromethene dye, a bright and photostable fluorophore which emits in fluorescein (FAM) channel. Unlike FAM, BDP FL is very photostable. Its brightness is similar to fluorescein. This alkyne can be conjugated with a number of azide-containing molecules by copper-catalyzed Click Chemistry
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DC36275 GHK-Cu acetate
GHK-Cu acetate is a complex of the tripeptide Gly-His-Lys and a copper(II) ion that has wound healing and anti-inflammatory activities. It increases proliferation and the levels of collagen and secreted pro-matrix metalloproteinase-2 (MMP-2) in isolated human fibroblasts. GHK-Cu increases levels of collagen and glycosaminoglycans (GAGs) and the expression of decorin in the wound tissue of rats. It decreases LPS-induced increases in the levels of reactive oxygen species (ROS), IL-6, and TNF-α in RAW 264.7 cells when used at a concentration of 10 μM.3 GHK-Cu (10 μg/g) prevents LPS-induced decreases in lung superoxide dismutase (SOD) activity and glutathione (GSH) levels and reduces LPS-induced increases in the number of cells and the level of total protein in bronchoalveolar lavage fluid (BALF) in a mouse model of acute lung injury.
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DC37216 Ethyl 2-naphthoate
Ethyl 2-naphthoate is a biochemical.
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DC37520 Naled
Naled is an organophosphate cholinesterase inhibitor that is used as an insecticide and as an acaricide.
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DC34162 Bronidox
Bronidox is an antimicrobial agent. It works by inhibiting enzyme activity in bacteria.
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