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Category: Reagents
Reference: OV-05
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Visikol for Plant Biology is designed as a direct replacement for Hertwig’s solution for use in rendering plant tissues transparent for microscopy. Using Visikol for Plant Biology was previously sold as “Visikol” by...
Reference: OV-15
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Visikol for Plant Biology is designed as a direct replacement for Hertwig’s solution for use in rendering plant tissues transparent for microscopy. Using Visikol for Plant Biology was previously sold as “Visikol” by...
Reference: OV-30
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Visikol for Plant Biology is designed as a direct replacement for Hertwig’s solution for use in rendering plant tissues transparent for microscopy. Using Visikol for Plant Biology was previously sold as “Visikol” by...
Reference: OV-100
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Visikol for Plant Biology is designed as a direct replacement for Hertwig’s solution for use in rendering plant tissues transparent for microscopy. Using Visikol for Plant Biology was previously sold as “Visikol” by...
Reference: VM-15
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Visikol MOUNT is a formulation of Visikol for Plant Biology that is designed to dry in order to form permanent mounts for microscopy slides.
Reference: VM-30
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Visikol MOUNT is a formulation of Visikol for Plant Biology that is designed to dry in order to form permanent mounts for microscopy slides.
Reference: VM-100
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Visikol MOUNT is a formulation of Visikol for Plant Biology that is designed to dry in order to form permanent mounts for microscopy slides.
Reference: H1-30
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With the Visikol HISTO tissue clearing approach you are now able to rapidly and easily image tissues in 3D without damaging the underlying cellular morphology. The Visikol HISTO approach has been designed to pair with...
Reference: H1-100
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With the Visikol HISTO tissue clearing approach you are now able to rapidly and easily image tissues in 3D without damaging the underlying cellular morphology. The Visikol HISTO approach has been designed to pair with...
Reference: H2-30
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With the Visikol HISTO tissue clearing approach you are now able to rapidly and easily image tissues in 3D without damaging the underlying cellular morphology. The Visikol HISTO approach has been designed to pair with...
Reference: H2-100
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With the Visikol HISTO tissue clearing approach you are now able to rapidly and easily image tissues in 3D without damaging the underlying cellular morphology. The Visikol HISTO approach has been designed to pair with...
Reference: HH-10
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With the Visikol HISTO tissue clearing approach you are now able to rapidly and easily image tissues in 3D without damaging the underlying cellular morphology. The Visikol HISTO approach has been designed to pair with...
Reference: HH-30
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With the Visikol HISTO tissue clearing approach you are now able to rapidly and easily image tissues in 3D without damaging the underlying cellular morphology. The Visikol HISTO approach has been designed to pair with...
Reference: HH-100
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With the Visikol HISTO tissue clearing approach you are now able to rapidly and easily image tissues in 3D without damaging the underlying cellular morphology. The Visikol HISTO approach has been designed to pair with...
Reference: HM-30
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With the Visikol HISTO tissue clearing approach you are now able to rapidly and easily image tissues in 3D without damaging the underlying cellular morphology. The Visikol HISTO approach has been designed to pair with...
Reference: HM-100
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With the Visikol HISTO tissue clearing approach you are now able to rapidly and easily image tissues in 3D without damaging the underlying cellular morphology. The Visikol HISTO approach has been designed to pair with...
Reference: HMSK-1
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With the Visikol HISTO tissue clearing approach you are now able to rapidly and easily image tissues in 3D without damaging the underlying cellular morphology. The Visikol HISTO approach has been designed to pair with...
Reference: HSK-1
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With the Visikol HISTO tissue clearing approach you are now able to rapidly and easily image tissues in 3D without damaging the underlying cellular morphology. The Visikol HISTO approach has been designed to pair with...
Reference: HSB-BK
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The Visikol HISTO Buffer Kit comes with all of the buffers required to complete the Visikol HISTO approach: 200 mL of Visikol HISTO Washing Buffer 10X, 100 mL of Visikol HISTO Penetration Buffer, 100 mL of Visikol...
Reference: HSK-AB-30
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The Visikol HISTO Antibody Buffer is used with immunolabeling in the Visikol HISTO tissue labeling approach. This solution is comprised of PBS/0.2% Tween 20/Heparin/3% donkey serum/5% DMSO.
Reference: HSK-AB-100
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The Visikol HISTO Antibody Buffer is used with immunolabeling in the Visikol HISTO tissue labeling approach. This solution is comprised of PBS/0.2% Tween 20/Heparin/3% donkey serum/5% DMSO.
Reference: HSK-BB-30
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The Visikol HISTO Blocking Buffer is used during the Visikol HISTO immunolabeling process. This solution is comprised of PBS/0.2% Tween™20/6% donkey serum/10% DMSO.
Reference: HSK-BB-100
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The Visikol HISTO Blocking Buffer is used during the Visikol HISTO immunolabeling process. This solution is comprised of PBS/0.2% Tween™20/6% donkey serum/10% DMSO.
Reference: HSK-PB-30
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Visikol HISTO Penetration Buffer is used with the Visikol HISTO immunolabeling process and is comprised of PBS / 0.2% Tween™20 / 0.3 M glycine / 20% DMSO.
Reference: HSK-PB-100
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Visikol HISTO Penetration Buffer is used with the Visikol HISTO immunolabeling process and is comprised of PBS / 0.2% Tween™20 / 0.3 M glycine / 20% DMSO.
Reference: HSK-PMB-30
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It is recommend that if you are trying to use Visikol HISTO-1 and Visikol HISTO-2 with larger, more collagenous, and difficult to clear tissues (e.g. liver tissue, archived human tissue, etc.) that you incubate...
Reference: HSK-PMB-100
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It is recommend that if you are trying to use Visikol HISTO-1 and Visikol HISTO-2 with larger, more collagenous, and difficult to clear tissues (e.g. liver tissue, archived human tissue, etc.) that you incubate...
Reference: HSK-WB-70
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The Visikol HISTO Washing Buffer 10X is used for the Visikol HISTO immunolabeling process. This solution is a concentrate and is comprised of: PPBS with 0.2% Tween-20 and 10µg/mL heparin. This solution should be...
Reference: HSK-WB-200
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The Visikol HISTO Washing Buffer 10X is used for the Visikol HISTO immunolabeling process. This solution is a concentrate and is comprised of: PPBS with 0.2% Tween-20 and 10µg/mL heparin. This solution should be...
Reference: HY-110179
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PSNCBAM-1 is a selective CB1 receptor allosteric antagonist with an EC50 of 0.1 μM. PSNCBAM-1 can be used in the researches of obesity.
Reference: HY-121835
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GLP-1R agonist 2 (compound 2) is a potent GLP-1R agonist. GLP-1R agonist 2 has the potential for the research of metabolic diseases like Type2 Diabetes and Obesity.
Reference: HY-120430
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HO-PEG14-OH is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
Reference: HY-112430
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TRPM8 antagonist 2 is a potent and selective TRPM8 antagonist, with an IC50 of 0.2 nM, used in the research of neuropathic pain syndromes.
Reference: HY-132158
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MC-AAA-NHCH2OCH2COO-7-aminomethyl-10-methyl-11-fluoro camptothecin (compound 21a), a camptothecin payload, can be conjugated to a monoclonal antibody (mAb) for the synthesis of camptothecin antibody-drug conjugate (ADC).
Reference: HY-Y0261AS1
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Ammonium sulphate,≥99.0%,AR-15N2 is the deuterium labeled Ammonium sulphate,≥99.0%,AR[1]. Ammonium sulphate,≥99.0%,AR is an inorganic sulfate salt used for molecular biology[2].
Reference: HY-N0548
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α-Angelica lactone is a naturally occurring anticarcinogen and an vinylogous nucleophile. α-Angelica lactone can give the chiral δ-amino γ,γ-disubstituted butenolide carbonyl derivatives and exhibitselectrophilic...
Reference: HY-15403
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Atrasentan (ABT-627) is an endothelin receptor antagonist with IC50 of 0.0551 nM for ETA.
Reference: HY-152536
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iNOS inhibitor-10 is an iNOS inhibitor (IC50: 65 nM). iNOS inhibitor-10 has antiproliferative effect against triple negative breast cancer cells.
Reference: HY-N0818
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Chikusetsusaponin IVa a major active ingredient of triterpenoid saponins, exerts antithrombotic effects, including minor hemorrhagic events.
Reference: HY-W041171
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3-Chloro-L-tyrosine is a specific marker of myeloperoxidase-catalyzed oxidation, and is markedly elevated in low density lipoprotein isolated from human atherosclerotic intima.
Reference: HY-D1269
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Rhodamine-N3 chloride is an azide-rhodamine fluorescent dye that can be used to label biomolecules containing alkyne groups.
Reference: HY-101909
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Val-Cit-PAB-MMAF is a agent-linker conjugate for ADC. Val-Cit-PAB-MMAF contains the ADCs linker (peptide Val-Cit-PAB) and a potent tubulin polymerization inhibitor MMAF (HY-15579)
Reference: HY-12755
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ML141 (CID-2950007) is a potent, allosteric, selective and reversible non-competitive inhibitor of Cdc42 GTPase. ML141 inhibits Cdc42 wild type and Cdc42 Q61L mutant with EC50s of 2.1 and 2.6 μM, respectively. ML141...
Reference: HY-147767
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PI3Kα-IN-6 (Compound 5b) is a PI3Kα inhibitor. PI3Kα-IN-6 exhibits anticancer potential and no toxicity in normal cells. PI3Kα-IN-6 increases generation of ROS, reduces mitochondrial membrane potential (MMP) and...
Reference: HY-W250174
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Lithium 3,5-diiodosalicylate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Reference: HY-W017277
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(+)-Menthol (D-Menthol) is one of the optical isomers of Menthol. (+)-Menthol can reduce the electrically evoked contractions of rat phrenic hemidiaphragm in vitro. Local anaesthetic activity. (+)-Menthol can also...
Reference: HY-100595
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Sodium stibogluconate (Stibogluconate trisodium nonahydrate) is a potent inhibitor of protein tyrosine phosphatase. Sodium stibogluconate inhibits 99% of SHP-1, SHP-2 and PTP1B activity at 10, 100, 100 μg/mL,...
Reference: HY-101311
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UPF-523 (AIDA), a rigid (carboxyphenyl) glycine derivative, is a relatively potent and selective antagonist of group I metabotropic glutamate receptors (mGlu1a) with an IC50 of 214 μM. But UPF-523 has no effect on...
Reference: HY-145888
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Antioxidant agent-2 (comp 3c), an BBB-penetrated antioxidant agent and a selective metal ions chelator, presents good neuroprotective effect and hepatoprotective effect for the study of Alzheimer’s disease.
Reference: HY-107260
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Lucidenic acid D (Lucidenic acid D2) is a highly oxidized lanostane-type triterpenoid.
Reference: HY-147584
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BTK-IN-14 is a potent inhibitor of BTK. BTK plays an important role in signaling mediated by B cell antigen receptor (BCR) and Fcγreceptor (FcγR) in B cells and myeloid cells, respectively. BTK-IN-14 has the potential...
Reference: HY-151701
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DiSulfo-Cy5 alkyne is a fluorescent dye can be used as a click chemistry reagent.
Reference: HY-B0863S2
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Glyphosate-d2-1 is the deuterium labeled Glyphosate[1]. Glyphosate is an herbicidal derivative of the amino acid glycine. Glyphosate targets and blocks a plant metabolic pathway not found in animals, the shikimate...
Reference: HY-N11663
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Dugesin C is a diterpenoid isolated from the plant Salvia dugesii with a spiro carbocyclic ring system derived from the normal neocrotane skeleton.
Reference: HY-115729
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PROTAC CDK9 ligand-1 is a CDK9 ligand that can be used in the synthesis of PROTACs.
Reference: HY-W014787S
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Decanedioic acid-d4 is the deuterium labeled Decanedioic acid[1]. Decanedioic acid, a normal urinary acid, is found to be associated with carnitine-acylcarnitine translocase deficiency and medium chain acyl-CoA...
Reference: HY-135636
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Ponatinib Acid, an analogue of Ponatinib, is usually used as a labeled chemical or fluorescent probe.
Reference: HY-154660
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N4-Benzoyl-2’-deoxy-5-iodocytidine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this process rely on...
Reference: HY-N6712
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Thiolutin (Acetopyrrothin) is a disulfide-containing antibiotic and anti-angiogenic compound produced by Streptomyces. Thiolutin inhibits the JAMM metalloproteases Csn5, Associated-molecule-with-the-SH3-Domain-of-STAM...
Reference: HY-19329
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HA130 is a selective autotaxin (ATX) inhibitor with an IC50 of 28 nM.
Reference: HY-133321
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N3-PEG24-Hydrazide is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
Reference: HY-139066
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Punicic acid is a bioactive compound of pomegranate seed oil. Punicic acid is an isomer of conjugated α-linolenic acid and a ω-5 polyunsaturated fatty acid. Punicic acid has the potential for the research of various...
Reference: HY-14249
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Bicalutamide is an orally active non-steroidal androgen receptor (AR) antagonist. Bicalutamide can be used for the research of prostate cancer.
Reference: HY-W010243S
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Methylisothiazolinone-d3 (hydrochloride) is the deuterium labeled Methylisothiazolinone (hydrochloride). Methylisothiazolinone hydrochloride is the constituent of the biocide Kathon CG. Methylisothiazolinone...
Reference: HY-N2492
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(E)-Methyl 4-coumarate (Methyl 4-hydroxycinnamate), found in several plants, such as Allium cepa or Morinda citrifolia L. leaves. (E)-Methyl 4-coumarate cooperates with Carnosic Acid in inducing apoptosis and killing...
Reference: HY-140722
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Mal-PEG-Succinimidyl Valerate (MW 20000) is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs.
Reference: HY-144341
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DprE1-IN-1 is a potent, orally active DprE1 inhibitor with favorable hepatocyte stability, low cytotoxicity and low hERG channel inhibition. DprE1-IN-1 displays potent?activity against both agent-susceptible and...
Reference: HY-W127495
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Methyl 10-Methylundecanoate is a biochemical reagent that can be used as a biological material or organic compound for life science related research.
Reference: HY-N8088
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Neolancerin is a natural product with weak cytotoxic activity against HL-60 cells.
Reference: HY-14299S
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Indacaterol-d3 is deuterium labeled Indacaterol.
Reference: HY-142099
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Hispaglabridin A is an antioxidant that is effective at inhibiting lipid peroxidation.
Reference: HY-W040239
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m-PEG6-CH2CH2COOH is a PEG-based based PROTAC linker can be used in the synthesis of PROTACs.
Reference: HY-147878
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Antibacterial agent 111 (Compound 3) is an antibacterial agent with MIC values of 3.90 μg/mL and 0.49 μg/mL against B. cereus and K. pneumonia, respectively. Antibacterial agent 111 firmly binds with tyrosyl-tRNA...
Reference: HY-17555
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Meclofenoxate hydrochloride, an ester of dimethylethanolamine (DMAE) and 4-chlorophenoxyacetic acid (pCPA), has been shown to improve memory, have a mentally stimulating effect, and improve general cognition.
Reference: HY-146342
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FAAH/MAGL-IN-3 (Compound 10) is an irreversible fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL) dual inhibitor with IC50 values of 179 and 759 nM against FAAH and MAGL, respectively....
Reference: HY-108317
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ABL127 is a selective and covalent inhibitor of protein methylesterase 1 (PME-1) with IC50s of 6.4 nM and 4.2 nM in HEK293T and MDA-MB-231 cells, respectively.
Reference: HY-18085
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Quercetin, a natural flavonoid, is a stimulator of recombinant SIRT1 and also a PI3K inhibitor with IC50 of 2.4 μM, 3.0 μM and 5.4 μM for PI3K γ, PI3K δ and PI3K β, respectively.
Reference: HY-B0590B
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(+)-Tetrabenazine ((+)-TBZ; (3R,11bR)-TBZ; (3R,11bR)-Tetrabenazine) is a reversible inhibitor of vesicular monoamine transporter 2 (VMAT-2), inhibits transport by VMAT2 with 10-fold greater potency than transport by...
Reference: HY-101466
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E7090 is an orally available, potent, and selective FGFR inhibitor with IC50s of 0.71 nM, 0.50 nM, 1.2 nM, and 120 nM for FGFR1/FGFR2/FGFR3/FGFR4, respectively.
Reference: HY-A0169
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Methyl aminolevulinate is an agent used as a sensitizer in photodynamic therapy (PDT). Methyl aminolevulinate is a proagent that can be metabolized to Protoporphyrin IX.
Reference: HY-148247
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BI-2081 is a GPR40 (FFAR1) partial agonist (EC50: 4 nM). BI-2081 induces glucose depending insulin secretion and reduces the plasma glucose concentration. BI-2081 can be used in the research of metabolic diseases, in...
Reference: HY-154437
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3’-β-Amino-2’,3’-dideoxy-5’-O-methoxy trityluridine is a purine nucleoside analog. Purine nucleoside analogs have broad antitumor activity targeting indolent lymphoid malignancies. Anticancer mechanisms in this...
Reference: HY-139987A
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LeuRS-IN-1 hydrochloride is a potent, orally active M. tuberculosis leucyl-tRNA synthetase (M.tb LeuRS) inhibitor. LeuRS-IN-1 hydrochloride has IC50 and Kd values of 0.06 μM, 0.075 μM for M.tb LeuRS, respectively....
Reference: HY-148382
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RI-962 is a potent and selective receptor-interacting protein kinase 1 (RIPK1) inhibitor. RI-962 inhibits RIPK1 with an IC50 value of 35.0 nM. RI-962 can be used for the research of nervous system diseases and...
Reference: HY-143800S
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S (+) Tolperisone-d10 is the deuterium labeled S (+) Tolperisone[1].
Reference: HY-N5004
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Guanfu base I (Acorine) is an active metabolite of Guanfu base A, isolated from Aconitum coreanum, and has a potent anti-arrhythmic effect.
Reference: HY-B1174
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Bekanamycin (Kanamycin B) is an aminoglycoside antibiotic produced by Streptomyces kanamyceticus, against an array of Gram-positive and Gram-negative bacterial strain.
Reference: HY-146337
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Dyrk1A/B-IN-1 (compound 3n) is a potent, selective and cell-permeable DYRK1A and DYRK1B inhibitor with Kis of 67.8 nM and 237.9 nM, and IC50s of 1.1 μM and 0.8 μM, respectively. Dyrk1A/B-IN-1 is not toxic to human...
Reference: HY-144260
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3CPLro-IN-1 (compound A17) is a potent and orally active inhibitor of SARS-CoV-2 3CLpro with an IC50 of 5.65 μM. 3-Chymotrypsin-like cysteine protease (3CLpro) is an indispensable protein in viral replication and...
Reference: HY-18299B
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(S)-Purvalanol B is the S enantiomer of Purvalanol B. Purvalanol B is a cyclin-dependent kinase inhibitor.
Reference: HY-15141G
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Staurosporine (AM-2282) (GMP) is Staurosporine (HY-15141) produced by using GMP guidelines. GMP small molecules works appropriately as an auxiliary reagent for cell therapy manufacture. Staurosporine is a potent,...
Reference: HY-112853
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Fosmidomycin sodium salt is a phosphonic acid antibiotic and a antimalarial agent, which is active against both Gram-negative and Gram-positive bacteria.
Reference: HY-114250
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Cantrixil (TRX-E-002-1), an active enantiomer of TRX-E-002, is a second-generation super-benzopyran (SBP) compound. Cantrixil increases phosphorylated c-Jun levels resulting in caspase-mediated apoptosis in ovarian...
Reference: HY-13284S
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7-α-Methylthio Spironolactone-d3 is the deuterium labeled 7-α-Methylthio Spironolactone[1].
Reference: HY-W007894
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Dimethylmalonic acid is a short-chain dicarboxylic acid in human serum. Dimethylmalonic acid is also a volatile organic compound detected in alveolar breath.
Reference: HY-19406
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AE-3763 is a peptide-based human neutrophil elastase inhibitor with an IC50 of 29 nM.
Reference: HY-W017442
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DL-Asparagine is a racemic melange of the Aparagine L and D-enantiomers. DL-Asparagine has been used in growth-media for bacteria-growth.