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| Cat. No. | Product Name | Field of Application | Chemical Structure |
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| DC36250 | NSC 34803 |
Thymohydroquinonee is a quinone that has been found in N. sativa seeds and has diverse biological activities. It scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH) free radicals and inhibits growth of A2780, OVCAR-8, CIS-A2780 ovarian cancer cells, and immortalized human ovarian epithelial cells. It is also active against P. falciparum in vitro.
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| DC37775 | Diisopropyl tartrate |
Diisopropyl tartrate is a reagent for kinetic resolution of racemic allylic alcohols and α-furfuryl amides by enantioselective epoxidation.
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| DC37342 | p-Methylbenzyl acetate |
p-Methylbenzyl acetate is a biochemical.
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| DC34218 | Cytochalasin D |
Cytochalasin D is a fungal metabolite. It blocks formation of contractile microfilament structures, resulting in multinucleated cell formation, reversible inhibition of cell movement, and the induction of cellular extrusion. It also inhibits actin polymerization, DNA synthesis, sperm motility, glucose transport, thyroid secretion, and growth hormone release.
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| DC34008 | BDP 630/650 X NHS ester |
BDP 630/650 is a borondipyrromethene fluorophore that has a high molar extinction coefficient, excellent quantum yield, and a relatively long lifetime of the excited state. Due to it, this fluorophore is useful for fluorescence polarization assays that allow to detect binding between molecules.
This is an amine reactive NHS ester. It contains an aminohexanoyl linker between the fluorophore and the reactive group.
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| DC37917 | Butalamine |
Butalamine is a vasodilator (peripheral) with local anesthetic effects. Butalamine has been shown to inhibit state 3 respiration and decrease ADP/O in rat liver.
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| DC36369 | Zelkovamycin |
Zelkovamycin is a cyclic peptide antibiotic that inhibits growth of X. oryzae, P. oryzae, S. aureus, and A. laidlawii in a concentration-dependent manner.
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| DC36860 | Mofebutazone |
Mofebutazone inhibits the immunological release of prostaglandins as well as leukotrienes.
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| DC37250 | n-Propyl methacrylate |
n-Propyl methacrylate is a plasticizer.
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| DC36922 | Metrafenone |
Metrafenone is a fungicide with protectant and curative properties, it is used for the control of powdery mildew in cereals and grape vines.
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| DC33761 | 2-Acetylpyrazine |
2-Acetylpyrazine is a pyrazine and a ketone. It is a yellow-brown powder at room temperature.
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| DC34684 | Hydrocortisone hemisuccinate anhydrous |
Hydrocortisone hemisuccinate anhydrous is an anti-inflammatory agent.
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| DC36579 | Tridecactide |
Tridecactide is a 13-amino acid peptide derived from proteolytic cleavage of Adrenocorticotropic hormone at the N-terminal of ACTH. ACTH (1-13) is amidated at the C-terminal to form ACTH (1-13)NH2 which in turn is acetylated to form alpha-MSH in the secretory granules. Alpha-MSH stimulates the synthesis and distribution of melanin in Melanocytes in mammals and Melanophores in lower vertebrates.
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| DC38068 | PYR-9588 |
PYR-9588, CAS#2199-58-8, is a useful intermediate for chemical synthesis of a number of biologically important molecules, including porphyrins, bile pigments, photosensitizers, anticancer drugs.
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| DC34182 | (R)-Citalopram oxalate |
(R)-Citalopram oxalate is a less active enantiomer of Escitalopram Oxalate, a potent and selective inhibitor of serotonin reuptake.
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| DC36439 | Bostrycin |
Bostrycin is an anthraquinone with antibacterial, antiproliferative, and phytotoxic properties. It is active against Gram-positive bacteria, including methicillin-resistant S. aureus (MRSA), M. tuberculosis, and C. botulinum. Bostrycin inhibits proliferation of A549 lung adenocarcinoma cells as well as halts the cell cycle at the G0/G1 phase and induces apoptosis in A549 cells. Bostrycin has been used as a cross-linking agent for protein immobilization that retains bacteriostatic activity when immobilized on nonwoven polypropylene fabric.
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| DC34011 | VPC-13566 |
VPC-13566 is an advanced BF3-specific small molecule that was previously reported to effectively inhibit AR transcriptional activity and to displace the BAG1L peptide from the BF3 pocket. VPC-13566 inhibits the growth of various prostate cancer cell lines, including an enzalutamide-resistant cell line, and reduces the growth of AR-dependent prostate cancer xenograft tumors in mice.
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| DC36158 | 3177 R.P. |
Melarsen oxide is a glutathione reductase inhibitor.
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| DC33894 | BDP R6G |
BDP R6G is a borondipyrromethene fluorophore whose absorption and emission spectra match those of rhodamine 6G (R6G) dye.
Thiol labeling is often an option of choice for the modification of proteins. Limited number of cysteine residues in proteins allow for more site-specific labeling than NHS ester labeling of amine groups, which are encountered in large number in many proteins.
This maleimide is a thiol reactive dye. Please refer to our recommended labeling protocol to achieve modification of your protein with this reagent.
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| DC33892 | BDP 630/650 Maleimide |
BDP 630/650 is a far red emitting borondipyrromethene based fluorophore for the Cyanine5 channel. Because of its relatively long lifetime of the excited state, this dye is particularly useful for fluorescence lifetime related measurements.
The reactive maleimide moiety allows to attach the dye to thiol groups in biomolecules, especially proteins and peptides.
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| DC33863 | BDP 630/650 azide |
BDP 630/650 azide is a bright and photostable dye azide for the far red region of the spectrum, for labeling using Click chemistry. This dye possesses a relatively long lifetime of the excited state, and can therefore be used for fluorescence polarization experiments.
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| DC33862 | BDP 581/591 |
BDP 581/591 is a bright and versatile fluorophore. It has a high brightness, significant two photon cross-section, and relatively long fluorescence lifetime.
The dye reacts with reactive oxygen species (ROS) with the change of its fluorescence. It can be therefore used for intracellular monitoring of ROS.
It can be used for the conjugation with both small molecules and biomolecules to construct tracers for fluorescence polarization assays and microscopy probes.
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| DC33948 | BDP TR amine |
BDP TR is a bright borondipyrromethene dye for ROX channel. Unlike ROX, it is very stable to oxidation. This amine derivative is useful for the conjugation with electrophilic reagents like epoxides and activated carboxyl derivatives, and as well for enzymatic transamination reaction.
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| DC35373 | BDP FL-PEG4-TCO |
BDP FL-PEG4-TCO is a fluorescent PEG derivative. PEG Linkers and derivatives may be useful in the development of antibody drug conjugates.
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| DC35370 | BDP FL-PEG4-amine TFA |
BDP FL-PEG4-amine TFA salt is a fluorescent PEG derivative. PEG Linkers and derivatives may be useful in the development of antibody drug conjugates.
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| DC33947 | BDP TMR amine |
BDP TMR is a dye for TAMRA channel. Unlike original TAMRA, it however possesses very good quantum yield, and therefore high brightness.
This derivative contains a primary amine group that can be conjugated with various electrophiles. It can also participate in enzymatic transamination reaction
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| DC33946 | BDP R6G amine |
BDP R6G is a borondipyrromethene dye matching Rhodamine 6G (R6G) channel. This derivative of the fluorophore contains aliphatic amine group in salt form.
The amine group can be conjugated with electrophiles. Amines can also used in enzymatic transamination.
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| DC33945 | BDP FL amine |
Amino derivative of BDP FL dye, a borondipyrromethene dye for FAM channel. This reagent possesses good aqueous solubility.
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| DC35159 | t-Boc-N-amido-PEG2-NHS ester |
t-Boc-N-amido-PEG2-NHS ester is a Boc PEG Linker. The Boc group can be deprotected in mildly acidic conditions. PEG Linkers may be useful in the development of antibody drug conjugates.
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| DC35764 | N-(Azido-PEG3)-NH-PEG3-acid HCl |
N-(Azido-PEG3)-NH-PEG3-acid HCl salt is a branched PEG derivative with a terminal azide group and terminal caboxylic acid. The amino group is reactive with carboxylic acids, activated NHS esters, and carbonyls. The azide group enables PEGylation via Click Chemistry. The terminal carboxylic acid can be reacted with primary amino groups in the presence of activators (e.g. EDC, or DCC) to form a stable amide bond.
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