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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC35182 | t-Boc-N-Amido-PEG2-propargyl |
t-Boc-N-Amido-PEG2-propargyl is a PEG derivative containing a propargyl group and Boc-protected amino group. The propargyl group can be reacted with azide-bearing compounds or biomolecules via copper catalyzed azide-alkyne Click Chemistry to yield a stable triazole linkage. The Boc group can be deprotected under mild acidic conditions to form the free amine.
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| DC36405 | FINO2 |
FINO2 is a ferroptosis-inducing peroxide compound that indirectly inhibits glutathione peroxidase 4 (GPX4) and oxidizes iron. It decreases GPX4 activity and protein levels in vitro but does not act as an active site, allosteric, or covalent inhibitor of GPX4 or alter GPX homeostasis. It also oxidizes iron in vitro, leading to degradation of the endoperoxide moiety, but does not affect the protein levels of iron regulatory proteins, such as IRP2, FTL1, or TFR. FINO2 induces lipid peroxidation of a large subset of the lipidome in HT-1080 cells when used at a concentration of 10 μM and induces ferroptosis in an arachidonic acid lipoxygenase-independent manner. It inhibits cell growth and induces lethality in the NCI-60 panel of cancer cell lines. It is selective for oncogenically transformed BJ-ELR cells over noncancerous BJ-hTERT cells. FINO2 induces oxidative stress, including lipid peroxidation, in RS4;11 B-lymphoblastic leukemia cells. It induces iron-dependent cell death, an effect that can be blocked by pretreatment with the lipophilic antioxidants ferrostatin-1 and liproxstatin-1 and does not induce markers of apoptosis, necrosis, or autophagy in RS4;11 cells.
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| DC37516 | Naphtox |
ANTU is an insecticide.
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| DC33802 | alpha-Naphthylacetic acid |
alpha-Naphthylacetic acid is a rooting agent and plant hormone in the auxin family. It is an ingredient in many commercial plant rooting horticultural products.
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| DC34155 | Sodium D-Pantothenate |
Sodium D-Pantothenate is a vitamin that performs an important role in the oxidation of fats and carbohydrates and certain amino acids. It is also a precursor in the biosynthesis of coenzyme A.
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| DC35024 | Benzyl-PEG5-amine |
Benzyl-PEG5-amine is a Benzyl PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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| DC35026 | Benzyl-PEG5-azide |
Benzyl-PEG5-azide is a PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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| DC35448 | Azido-PEG4-alcohol |
Azido-PEG4-alcohol is a PEG derivative containing an azide group and a terminal hydroxyl group. The hydrophilic PEG spacer increases solubility in aqueous media. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.
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| DC35999 | Thiol-PEG8-acid |
Thiol-PEG8-acid is a PEG derivative containing a thiol group and a terminal carboxylic acid. The hydrophilic PEG spacer increases solubility in aqueous media. The thiol group reacts with maleimide, OPSS, vinylsulfone and transition metal surfaces including gold, silver, etc. 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.
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| DC37110 | 1-Nitronaphthalene |
1-Nitronaphthalene is a biochemical.
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| DC35447 | Azido-PEG3-alcohol |
Azido-PEG3-alcohol is a PEG derivative containing an azide group and a terminal hydroxyl group. The hydrophilic PEG spacer increases solubility in aqueous media. The azide group can react with alkyne, BCN, DBCO via Click Chemistry to yield a stable triazole linkage. The hydroxyl group enables further derivatization or replacement with other reactive functional groups.
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| DC37676 | JWH-249 |
JWH 249 is a synthetic cannabinoid (CB) that potently activates the central CB1 and peripheral CB2 receptors (Ki = 8.4 and 20 nM, respectively).
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| DC37675 | JWH-167 |
JWH 167 is a synthetic cannabinoid (CB) with moderate affinities for both central CB1 (Ki = 90 nM) and peripheral CB2 (Ki = 159 nM) receptors. Its physiological and toxicological properties are not known. This product is intended for forensic and research purposes.
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| DC35267 | Fmoc-NH-ethyl-SS-propionic acid |
Fmoc-NH-ethyl-SS-propionic acid is a cleavable PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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| DC34628 | Salicyl-AMS |
Salicyl-AMS is a MbtA Inhibitors and Antimycobacterial Agent. salicyl-AMS [5'-O-(N-salicylsulfamoyl)adenosine] inhibits M. tuberculosis growth in vitro under iron-limited conditions.
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| DC37118 | N-Nitrosodiphenylamine |
N-Nitrosodiphenylaμmine is used to make rubber products such as tires or to make other chemicals.
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| DC34106 | N106 |
N106 directly activates the SUMO-activating enzyme, E1 ligase, and triggers intrinsic SUMOylation of SERCA2a. Decreased activity and expression of the cardiac sarcoplasmic reticulum calcium ATPase (SERCA2a), a critical pump regulating calcium cycling in cardiomyocyte, are hallmarks of heart failure.
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| DC34346 | LT175 |
LT175 is a PPARα/γ ligand with potent insulin sensitizing effects and reduced adipogenic properties.
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| DC37253 | 9-Ethylcarbazole |
9-Ethylcarbazole is a biochemical.
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| DC35020 | Benzyl-PEG5-alcohol |
Benzyl-PEG5-alcohol is a Benzyl PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates or drug delivery methods.
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| DC34647 | Mirodenafil Dihydrochloride |
Mirodenafil belongs to the drug class PDE5 inhibitors, which includes avanafil, sildenafil, tadalafil, udenafil, and vardenafil, and is the first-line treatment for erectile dysfunction.
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| DC36750 | BF3DNCA methyl ester |
Herkinorin is an opioid analgesic that is an analogue of the natural product Salvinorin A. Unlike Salvinorin A which is a selective κ-opioid agonist with no significant μ-opioid receptor affinity, herkinorin is a μ-opioid agonist with more than 100x higher μ-opioid affinity and 50x lower κ-opioid affinity compared to Salvinorin A. Herkinorin is a semi-synthetic compound, made from Salvinorin B, which is most conveniently made from Salvinorin A by deacetylation, as while both Salvinorin A and Salvinorin B are found in the plant Salvia divinorum, Salvinorin A is present in larger quantities.
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| DC34679 | Indigotindisulfonate sodium |
Indigotindisulfonate sodium is an indolesulfonic acid used as a dye in renal function testing for the detection of nitrates and chlorates, and in the testing of milk.
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| DC34105 | PF-3187207 |
Latanoprostene, also known as PF-3187207, is a a nitric oxide (NO)-donating latanoprost with prostaglandin activity. It loweres intraocular pressure (IOP) more effectively than latanoprost in monkeys, dogs and rabbits.
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| DC35160 | t-Boc-N-amido-PEG4-NHS ester |
t-Boc-N-amido-PEG4-NHS ester is a PEG derivative containing an NHS ester and a Boc-protected amino group. The Boc group can be deprotected under mild acidic conditions to form the free amine. The NHS ester can be used to label the primary amines (-NH2) of proteins, amine-modified oligonucleotides, and other amine-containing molecules. PEG Linkers may be useful in the development of antibody drug conjugates.
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| DC37629 | C.I. Food Yellow 10 |
C.I. Food Yellow 10, also known as Fast Yellow AB or Acid Yellow, is an azo dye used primarily as a food dye that is now delisted in both Europe and USA and is forbidden if used in foods and drinks. Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for human consumption or therapeutic use.
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| DC35299 | DNP-PEG4-NHS ester |
DNP-PEG4-NHS ester is a PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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| DC35297 | DNP-PEG4-acid |
DNP-PEG4-acid is a PEG Linker. PEG Linkers may be useful in the development of antibody drug conjugates.
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| DC34397 | (-)-Quinpirole hydrochloride |
(-)-Quinpirole HCl is the most widely used D2 agonist in in vivo and in vitro studies.
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| DC38039 | Lithium guanosine triphosphate |
Lithium guanosine triphosphate functions as a carrier of phosphates and pyrophosphates involved in channeling chemical energy into specific biosynthetic pathways. GTP activates the signal transducing G proteins which are involved in various cellular processes including proliferation, differentiation, and activation of several intracellular kinase cascades. Proliferation and apoptosis are regulated in part by the hydrolysis of GTP by small GTPases Ras and Rho. Another type of small GTPase, Rab, plays a role in the docking and fusion of vesicles and may also be involved in vesicle formation. In addition to its role in signal transduction, GTP also serves as an energy-rich precursor of mononucleotide units in the enzymatic biosynthesis of DNA and RNA.
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