Alternate TextTo enhance service speed and avoid tariff delays, we've opened a US warehouse. All US orders ship directly from our US facility.
Home > Inhibitors & Agonists > Others

Others

You can also try the following methods, and our professionals will serve you Customized Consultation
Cat. No. Product Name Field of Application Chemical Structure
DC35628 SPDP acid
SPDP acid is a non-PEG crosslinker.
More description
DC36556 Dodecyl benzene sulfonic acid
Dodecyl benzene sulfonic acid, Dopant for conducting polymers strong acid catalyst for amino cross-linked coatings.
More description
DC34443 Cilostamide
Cilostamide is a selective inhibitor of type III phosphodiesterase (PDE3).
More description
DC34748 DSS Crosslinker
DSS crosslinker, or Disuccinimidyl suberate, is a homobifunctional crosslinker that is cell membrane permeable. DSS crosslinker has amine-reactive NHS esters at both ends of an 8-atom (11.4 angstrom) spacer arm that are used to conjugate proteins. DSS crosslinker can be used to conjugate or crosslink intracellular proteins.
More description
DC36365 Rugulotrosin A
Rugulotrosin A is an antibiotic active against the Gram-positive bacteria E. faecalis, B. cereus, B. subtilis, and S. aureus. Rugulotrosin A is inactive against Gram-negative bacteria.
More description
DC36246 4-oxo Withaferin A
4-oxo Withaferin A is a derivative of the steroidal lactone withaferin A that has anticancer activity. It is cytotoxic to A2780 ovarian cancer cells and carboplatin-resistant A2780 (A2780/CP70) cells and is 4.4-fold selective for A2780 cells over non-cancerous ARPE19 cells.
More description
DC37554 Arotinolol hydrochloride
Arotinolol (INN, marketed under the tradename Almarl) is a medication in the class of mixed alpha/beta blockers. It also acts as a β3 receptor agonist. A 1979 publication suggests arotinolol as having first been described in the scientific literature by Sumitomo Chemical as "β-adrenergic blocking, antiarrhythmic compound S-596".
More description
DC34528 Micheliolide
Micheliolide is a natural, irreversible activator of pyruvate kinase M2, and a suppressor of leukemia cells.
More description
DC33771 Bitriben
Bitriben is an anthelmintic agent.
More description
DC36945 Cloricromen
Cloricromen is a platelet aggregation inhibitor.
More description
DC33828 Mercaptoacetic acid
Mercaptoacetic acid is a protecting agent for tryptophan in amino acid analysis and indicator of acidicty. It is an intermediate in the chemical reactions such as addition, elimination and cyclization. It acts as a precursor to ammonium thioglycolate, sodium thioglycolate and calcium thioglycolate.
More description
DC35486 PEG12
PEG12 is a PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
More description
DC33407 Carbadoxum
Carbadox is a livestock anitbiotic and growth promoter. It is particularly effective in treating swine dysentery and enteritis. However, its use has been prohibited in the UK following reports of carcinogenicity and mutagenicity.
More description
DC36603 Deacylketoconazole
Deacylketoconazole is a Ketoconazole derivative. Ketoconazole is an antifungal medication which is used primarily to treat fungal infections.
More description
DC35487 PEG13
PEG13 is a PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
More description
DC34187 Gly-Pro-Arg-Pro Acetate
Gly-Pro-Arg-Pro Acetate is an inhibitor of fibrinogen aggregation that acts by binding to fibrinopeptide A.
More description
DC35590 m-PEG7-4-nitrophenyl carbonate
m-PEG7-4-nitrophenyl carbonate is a PEG Linker
More description
DC37549 Triamcinolone diacetate
Triamcinolone diacetate is a Lysyl oxidase antagonist.
More description
DC35223 Bromo-PEG5-bromide
Bromo-PEG5-bromide is a PEG derivative containing two bromide groups. The bromide (Br) is a very good leaving group for nucleophilic substitution reactions. The hydrophilic PEG spacer increases solubility in aqueous media.
More description
DC37753 Amastatin
Amastatin is a non-toxic inhibitor of aminopeptidase A (Ki = 1 μM) and leucine aminopeptidase. Also acts as a slow-binding, competitive inhibitor of aminopeptidase M. Does not inhibit aminopeptidase B, chymotrypsin, elastase, papain, pepsin, thermolysin, or trypsin.
More description
DC37921 Fenpropimorph
Fenpropimorph is a small moluecule fungicide.
More description
DC35394 Fmoc-NH-PEG11-CH2COOH
Fmoc-NH-PEG11-CH2COOH is a PEG derivative containing an Fmoc-protected amine and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The Fmoc group can be deprotected under basic conditions to obtain the free amine which can be used for further conjugations. The terminal carboxylic acid can be reacted with primary amine groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.
More description
DC34099 Oe-9000
Oe-9000 is a novel blocker of voltage-gated Na(+) currents in neurons. It reversibly reduces slowly activating and inactivating tetrodotoxin-resistant (TTX-R) Na(+) currents as well as rapidly activating and inactivating TTX-sensitive (TTX-S) Na(+) currents at low micromolar concentrations.
More description
DC34696 Hydramethylnon
Hydramethylnon is an insecticide primarily used for fire ants. It is poorly absorbed in the mammal body and leaves mostly unchanged.
More description
DC33716 Acetyl ketene
Diketene, also known as Acetyl ketene, is used as a chemical intermediate for acetoacetic esters and acetoacetanilides, dyes, pharmaceuticals, food preservatives, and insecticides.
More description
DC37466 Alclometasone
Alclometasone is a topical corticosteroid.
More description
DC34438 Blebbistatin
(±)-Blebbistatin is a cell cycle inhibitor and a selective inhibitor of non-muscle myosin II.
More description
DC36696 Decarboxylated S-adenosyl methionine Sulfate
S-Adenosyl-3-methylthiopropylamine is a substrate that is involved in the biosynthesis of polyamines including spermidine, spermine, and thermospermine.
More description
DC36107 (±)-Alphamethrin
alpha-Cypermethrin is a synthetic pyrethroid pesticide.
More description
DC36609 3-Deazaadenosine
3-Deazaadenosine is a potent inhibitor of adenosine deaminase, an enzyme that catalyzes the removal of the amine group from adenosine. This compound exhibits antitumor activity against a range of leukemia cell lines. 3-Deazaadenosine is an inhibitor of SAHH.
More description

Customized Consultation X

Your information is safe with us. * Required Fields.

Your name
Company
Email
Procuct Name
Cat. No.
Remark
Verification code
Please fill out the characters in the picture
X