Recently Updated Products
Browse the 100 most recently updated products.
Recently Updated Products list
- GC16450Prednisone
Glucocorticoid receptor agonist
- GC74216AF488 DBCO ditriethylamine
AF488 DBCO ditrietlamine is the ditrietlamine salt form of AF488 DBCO.
- GC111391-Stearoyl-2-Arachidonoyl-sn-glycero-3-PC
A phospholipid
- GC59006Azide-PEG4-Amine
Oligoethylene glycols are versatile hydrophilic linkers. Each monomer has a length of 3.43 Å, so that the length of PEG4 is around 14 Å (1.4 nm). Azide-PEG4-Amine is a bifunctional compound with an amine group that can be modified by acylation by activated esters or similar carbonyl compounds, and an azide group that is suitable for Click chemistry reactions. PEG4 is highly hydrophilic and biocompatible.
- GC49003(E)-Ajoene
A disulfide with diverse biological activities
- GC4652722-NBD Cholesterol
A fluorescent cholesterol analog
- GC45937trans-β-Ocimene
A monoterpene
- GC12153Zebularine
Zebularine, a cytidine lacking the 4-amino group, is a DNMT inhibitor that inhibits DNA methylation.
- GC14683Sunitinib malate
A multi-kinase inhibitor
- GF03018T4 DNA Ligase(with 10X Ligation Buffer)
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- GC26270Bovine Serum Albumin(Fatty Acid & lgG Free)
Bovine Serum Albumin(Fatty Acid & lgG Free) is a globular protein and oligonucleotide-binding protein composed of 583 amino acid residues and consisting of three identical α-helical domains.
- GC13118Dihydro-β-erythroidine hydrobromide
Dihydro-β-erythroidine (DHβE) hydrobromide is a potent, orally active, and competitive antagonist of neuronal nAChRs.
- GC70439PF-739
PF-739 is an AMPK activator. PF-739 reduces plasma glucose levels by activating all 12 heterotrimeric AMPK complexes.
- GC65429Capillarisin
Capillarisin, as a constituent from Artemisiae Capillaris herba, is found to exert anti-inflammatory and antioxidant properties.
- GC19973Poly-D-lysine hydrobromide (M.W 70000~150000)
Poly-D-lysine hydrobromide (MW 70,000 ~ 150,000) is a cell non-specific attachment factor that is often used to promote the adhesion of cells to solid matrices.
- GC26535NRG1-beta 1 Protein, Human
NRG-1 protein, belonging to the structurally related peptide growth factor family of Human, originates from alternative splicing genes and induces Fn14 expression in MCF7 cells.
- GC79400SIYNFEKL acetate
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- GC49480Salicylic Acid-d4
Salicylic Acid-d4 is the deuterium labeled 2-Carboxyphenol.
- GC65915TLR7/8 agonist 4
TLR7/8 agonist 4 (compound 41) is a potent TLR7/8 agonist. TLR7/8 agonist 4 has anti-cancer activity.
- GC78914TTP-6171
TTP-6171 is a non-covalent inhibitor of Monkeypox virus I7L protease, and it can be used for research on poxvirus infections [1] .
- GC19526Cyclic di-GMP disodium
Cyclic di-GMP disodium is a cyclic dinucleotide signaling molecule synthesized by bacteria and is a STING agonist.
- GB60339Palladium (II) acetate
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- GC69329KDM5-C49 hydrochloride
KDM5-C49 (KDOAM-20) hydrochloride is an effective and selective inhibitor of KDM5 demethylases, with IC50 values of 40 nM, 160 nM, and 100 nM for KDM5A, KDM5B, and KDM5C respectively. It can be used in cancer research.
- GC43305Compound 48/80 (hydrochloride)
Compound 48/80 trihydrochloride is a mixture of condensation products of N-methyl-p-methoxyphenethylamine with formaldehyde.
- GC11908Cisplatin
Cisplatin, a platinum-containing anticancer drug, is one of the most commonly used cytotoxic agents for the treatment of a variety of solid malignant tumors.
- GC41390Aldosterone
Aldosterone is a steroid hormone secreted by the adrenal cortex and is the principle mineralocorticoid controlling sodium and potassium balance
- GC39080Spathulenol
Spathulenol is isolated from Psidium guineense Sw, and has antioxidant, anti-inflammatory, antiproliferative and antimycobacterial activities. Spathulenol shows a high antioxidant activity with an IC50 of 85.60 μg/mL in the DPPH system.
- GB60317Oleyl oleate
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- GC18147Tretinoin (Aberela)
Tretinoin (Aberela)is a vitamin A-derived, non-peptidic, small lipophilic molecule that acts as a ligand for nuclear RA receptors (RARs), with a K d value of 17nM for PPARβ/δ.
- GC15307SU5416
SU5416 is a small-molecule Flk-1/KDR inhibitor that inhibits autophosphorylation of the Flk-1 receptor, with an IC 50 value of 1.23μM.
- GC39451Testosterone (propionate)
Testosterone propionate is a slower releasing anabolic steroid used mainly in the treatment of low testosterone levels in men.
- GC26716Polyvinylpyrrolidone (PVP) (M.W.~360000)
Used in molecular biology, nucleic acid hybridization tested, mol wt 360,000
- GC68230MitoSOX Red
MitoSOX Red is a live cell fluorescent probe targeting mitochondria with maximum excitation/emission light of 510/580 nm.
- GC30535Transdermal Peptide (TD 1 (peptide))
Transdermal Peptide (TD 1 (peptide)) is a peptide chaperon with high permeability that facilitates several proteins' transdermal delivery via topical co-administration.
- GC49790Reuterin
Reuterin is a broad-spectrum antimicrobial small molecule produced by Lactobacillus reuteri during anaerobic fermentation of glycerol.
- GC16879Tubercidin
Tubercidin is an adenosine analog with potent antimycobacterial and antitumor bioactivities.
- GN10388Gallic acid
Gallic acid is a 3,4,5-trihydroxybenzoic acid phenolic compound with antioxidant, anti-inflammatory and antitumor activities.
- GK10040One-step TUNEL Apoptosis Detection Kit (Green, FITC)
One-step TUNEL Apoptosis Detection Kit (Green, FITC) provides a fast and highly efficient method for detecting the degree of nuclear DNA fragmentation in cells and tissues during apoptosis, Ex/Em = 492/517nm.
- GK10041One-step TUNEL Apoptosis Detection Kit (Orange, CY3)
One-step TUNEL Apoptosis Detection Kit (Orange, CY3) provides a fast and highly efficient method for detecting the degree of nuclear DNA fragmentation in cells and tissues during apoptosis, Ex/Em = 550/570nm.
- GC30950TTA-Q6
TTA-Q6 is a selective antagonist of T-type Ca2+ channel and can be used in neurological research.
- GC10893Dutasteride
5-alpha-reductase inhibitor
- GP10065Endomorphin-1
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- GC19377Visomitin (SKQ1)
Visomitin is a new antioxidant with the highest mitochondrion membrane penetrating ability and potent antioxidant capability.
- GC12512Losartan Carboxylic Acid
Losartan Carboxylic Acid is a human active metabolite of the angiotensin II receptor type 1 (AT1) receptor antagonist losartan, with an IC 50 of 139.3μM for inhibiting cAMP PDE (phosphodiesterase) activity.
- GC11008Necrostatin-1
Necrostatin-1 is a novel small molecule inhibitor of necroptosis. Necrostatin-1 inhibits RIP1 kinase activity (EC 50 =182nM) through allosteric binding.
- GC10854IDE 2
IDE 2 is a definitive endoderm inducer with small molecule activity and activates the TGF-β/Nodal signaling pathway.
- GC61473Trastuzumab deruxtecan
Trastuzumab deruxtecan is a human epidermal growth factor receptor 2 (HER2)-targeted antibody-drug conjugate (ADC) composed of a humanized anti-human HER2 (anti-hHER2) antibody, an enzymatically cleavable peptide linker, and a topoisomerase I inhibitor (DX-8951 derivative).
- GB57802Cobalt(II)nitratehexa hydrate
Cobalt(II)nitratehexa hydrateis a cobalt ion source and common starting material used for synthesizing various cobalt-containing compounds.
- GF15503Carpinontriol B
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- GC50492OB-1
OB-1 is a potent stomatin-like protein-3 (STOML3) inhibitor that inhibits Piezo1 currents with an IC 50 value of 10nM.
- GC11074BIBP 3226 trifluoroacetate
BIBP 3226 trifluoroacetate is a potent non-peptide neuropeptide Y (NPY) Y1 receptor antagonist with K i values of 1.1, 79, and 108nM for rNPY Y1, hNPFF2, and rNPFF, respectively.
- GC12793RITA (NSC 652287)
RITA (NSC 652287) is a tricyclic thiophene derivative that binds to p53dN (K d =1.5nM) and blocks the p53-HDM-2 interaction, thereby inhibiting p53 ubiquitination.
- GK10027Bradford Protein Quantification Kit
The Bradford Protein Quantification Kit is a kit for rapid determination of protein concentrations in the range of 0.025-2mg/ml.
- GC69899SIRT6 activator 12q
SIRT6 activator 12q is a selective SIRT6 activator (IC₅₀ = 0.58μM).
- GC44085L-Sulforaphene
L-Sulforaphene is a natural isothiocyanate with anti-inflammatory, anticancer, and antioxidant effects.
- GC70717Benitrobenrazide (Hexokinase 2 inhibitor 1)
Benitrobenrazide (Hexokinase 2 inhibitor 1) inhibits glycolysis by directly targeting HK2.
- GC43367D-(+)-Glucose-13C6
D-(+)-Glucose-13C6 is the stable isotope labeled counterpart of D-(+)-Glucose and is mainly used as an internal standard for the quantification of D-(+)-Glucose by GC- or LC-MS measurement.
- GC69706PI3K/AKT-IN-1
PI3K/AKT-IN-1 is a potent PI3K/AKT dual inhibitor with IC 50 values of 6.99μM, 4.01μM, and 3.36μM for PI3Kγ, PI3Kδ and AKT, respectively.
- GC33044RMC-4550
RMC-4550 is an orally active allosteric inhibitor of SHP2 (IC₅₀=0.583nM).
- GA22584Hippuryl-Arg-OH
Hippuryl-Arg-OH is a fluorescent signal substrate used in enzyme activity assays for the identification and cleavage of peptide bonds containing arginine.
- GC16591d[Cha4]-AVP
d[Cha4]-AVPis a potent and selective Vasopressin (AVP) V1b receptor agonist with a K i value of 1.2nM, 151nM for V1b and V1a receptors, respectively.
- GC40758Gly-Phe-β-naphthylamide
Gly-Phe-β-naphthylamide is a cathepsin C substrate and lysosomal perturbing agent.
- GC18157Thymoquinone
Thymoquinone is an orally active natural product isolated from Nigella glandulifera .
- GB57006Ammonium iron(II) sulfate hexahydrate
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- GC32921LOM612
LOM612 is a potent FOXO relocator, with an EC50 value of 1.5 μM in U2fox RELOC cells.
- GC80849AtPep1 TFA
AtPep1 TFA is an endogenous inducer of innate immune responses.
- GC71375GPR61 Inverse agonist 1
GPR61 Inverse agonist 1 (Compound 1) is a GPR61 inverse agonist (IC50: 11 nM).
- GC27810Convolamine
Convolamine is an alkaloid found in Convolvulus pluricaulis and an effective positive modulator of the sigma-1 receptor (IC 50 = 289 nM), exhibiting cognitive and neuroprotective properties.
- GC31636Cholesteryl linoleate
A cholesterol ester
- GB60393Perfluorooctanesulfonamide
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- GC81902SR10098
SR10098 is a benzimidazole-based Nurr1 activator with an EC 50 of 24 nM against full-length Nurr1.
- GC81906N-Phenyl-1H-benzimidazol-6-amine
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- GC819045MPEP
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- GC81903Zaloganan acetate
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- GN10700Plantamajoside
Plantamajoside is a phenylpropanoid glycoside compound with NF-κB and MAPK signaling pathway inhibition and antioxidant activity.
- GC11108Abiraterone acetate
A CYP17A1 inhibitor
- GC81901M918 acetate
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- GC81905α-Methyl-L-tryptophan
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- GC39005Nordalbergin
Nordalbergin, a coumarin isolated from the wood bark of Dalbergia sissoo. Nordalbergin shows strong activity in the induction of differentiation of HL-60.
- GC37999β-Anhydroicaritin
β-Anhydroicaritin is isolated from Boswellia carterii Birdware, has important biological and pharmacological effects, such as antiosteoporosis, estrogen regulation and antitumor properties.
- GC39731Warfarin sodium
Warfarin sodium is an orally active vitamin K antagonist.
- GC19992Clodronate Liposomes
Macrophage scavenger - Clodronate Liposomes Clodronate Liposomes were developed by Professor Nico van Rooijen of Vrije University in Amsterdam, Netherlands, introduces membrane-impermeable clodronate into the cell through the entosis mechanism of macrophages. Under the action of macrophage lysosomal phosphatase, clodronate dissolved in the aqueous phase of liposomes is released and accumulated in the cells. When it reaches a certain concentration, it can induce macrophages to enter the apoptosis process, and then the macrophages were eliminated. Clodronate Liposomes are suitable for various injection methods, such as intravenous injection, intraperitoneal injection, subcutaneous injection, intranasal injection and testicular injection, etc. The injection volume is related to the body weight of the mice, the injection period, the injection method and the purpose of the experiment. Solution 10 mM Na 2 HPO 4 , 10 mM NaH 2 PO 4 , 140 mM NaCl Concentration 5 mg/mL Lipid composition Phosphatidylcholine and cholesterol Structure
- GC27581Control Liposomes(PBS)
Disodium clodronate is a specific macrophage-killing agent that can eliminate macrophages in tissues by inducing macrophage apoptosis.
- GC494437α-hydroxy Cholesterol
7α-hydroxy Cholesterol is an endogenous oxidized cholesterol metabolite.
- GC31360Taspoglutide (ITM077)
Taspoglutide (ITM077) is a novel analog of human glucagon-like peptide-1 [hGLP-1(7-36)NH 2 ] in clinical development for the treatment of type 2 diabetes. Taspoglutide inhibits VEGFR2 in CHO cells with an IC 50 value of 4.6±0.6nM.
- GC70621NBD-Pen
NBD-Pen is a high-sensitivity, specific fluorescence probefor lipid radicals (λex: 478 nm, λem: 534 nm).
- GC15161Calcium D-Panthotenate
Calcium D-Panthotenate (Vitamin B5 calcium salt), a vitamin, can reduce the patulin content of the apple juice.
- GC14927Trazodone HCl
Trazodone (hydrochloride) (AF-1161) is an antidepressant belonging to the class of serotonin receptor antagonists and reuptake inhibitors for treatment of anxiety disorders.
- GC26002Trazodone
Trazodone is a 5-hydroxytryptamine antagonist and reuptake inhibitor (SARI).
- GC30112PAT-1251
PAT-1251 is a lysyl oxidase-like 2 (LOXL2; IC 50 =0.71μM) inhibitor.
- GC4078111(Z),14(Z),17(Z)-Eicosatrienoic Acid
11(Z),14(Z),17(Z)-Eicosatrienoic Acid is an ω-3 long-chain polyunsaturated fatty acid and an endogenous metabolite, can serve as a metabolic intermediate in the conversion of α-linolenic acid to long-chain ω-3 fatty acids such as EPA and DHA.
- GC13645nor-Binaltorphimine dihydrochloride
nor-Binaltorphimine dihydrochloride is a potent and selective κ opioid receptor (KOR) antagonist.
- GC63604Sparfosic acid
Sparfosic acid, a DNA antimetabolite agent, is a potent inhibitor of aspartate transcarbamoyl transferase, the enzyme catalyzing the second step of de novo pyrimidine biosynthesis.
- GC33094GC7 Sulfate
GC7 Sulfate is the sulfate salt of N1-guanyl-1,7-diaminoheptane and a deoxyhypusine synthase (DHPS) inhibitor.
- GC30183Acridine Orange 10-Nonyl Bromide (Nonylacridine orange)
Acridine Orange 10-Nonyl Bromide (Nonylacridine orange) is a mitochondria-targeting fluorescent probe (excitation wavelength: 489nm; emission wavelength: 525nm).
- GC62372Cyclic-di-GMP sodium
Cyclic-di-GMP sodium is a STING agonist and a bacterial second messenger that coordinates different aspects of bacterial growth and behavior, including motility, virulence, biofilm formation, and cell cycle progression. Cyclic-di-GMP sodium has anti-cancer cell proliferation activity and also induces elevated CD4 receptor expression and cell cycle arrest. Cyclic-di-GMP sodium can be used in cancer research.
- GC60186HBC620
HBC620 is an HBC-like fluorophore, a GFP fluorophore-like synthetic dye, with a maximum excitation wavelength of 577nm and a maximum emission wavelength of 620nm.
- GC502444-ethynyl-N-ethyl-1,8-naphthalimide
Click-activated fluorescent probe
- GN10341Acetate gossypol
Acetate gossypol is a lipid-soluble polyphenolic compound extracted from the cotton plant with antifertility, antioxidant, and anticancer properties.
- GN10082Gossypol
Gossypol is a lipid-soluble polyphenolic compound extracted from the cotton plant with antifertility, antioxidant, and anticancer properties.
