others
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- Reagents(34)
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- Others(296)
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- Cat.No. Product Name Information
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BCC6724
Physostigmine hemisulfate
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BCC1562
Etimizol
Etimizol(Ethymisole; Antiffine; Ethylnorantifein) was shown to relieve amnesia effectively in the origin of which there is the hypoxic component (hypobaric hypoxia, actinomycin D, mechanical injury of the brain).
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BCC1587
GANT 58
GANT 58 is a potent Gli antagonist that inhibits GLI1-induced transcription with IC50 of 5 μM.
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BCC5321
Tetrahydropapaverine HCl
Tetrahydropapaverine hydrochloride is one of the Tetrahydroisoquinolines. Tetrahydropapaverine hydrochloride has neurotoxic effects on dopamine neurons.
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BCC2033
VcMMAE
VcMMAE (mc-vc-PAB-MMAE) is a drug-linker conjugate for ADC with potent antitumor activity by using the anti-mitotic agent, monomethyl auristatin E (MMAE, a tubulin inhibitor), linked via the lysosomally cleavable dipeptide, valine-citrulline (vc).
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BCC6352
1,9-Dideoxyforskolin
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BCC8096
Cinaciguat hydrochloride
Potent soluble guanylyl cyclase (sGC) activator,Cinaciguat hydrochloride is a potent soluble guanylate cyclase (GC) activator with EC50 of 15 nM in platelets.
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BCC3821
Nicotine Difartrate
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BCC8006
Acridine Orange hydrochloride
Acridine orange is a cell-permeable fluorescent dye that binds to nucleic acids, resulting in an altered spectral emission.
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BCC5203
VGX-1027
VGX-1027(GIT27) is an isoxazole compound that exhibits various immunomodulatory properties; reduce the secretion of IL-1beta, TNF-alpha and IL-10 from purified murine macrophages.
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BCC4418
NGR peptide
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BCC4489
Dienogest
Dienogest(STS-557) is a specific progesterone receptor agonist with potent oral endometrial activity and is used in the treatment of endometriosis.
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BCC7724
(5Z)-7-Oxozeaenol
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BCC3769
Docosanol (Abreua)
1-Docosanol is a saturated fatty alcohol used traditionally as an emollient, emulsifier, and thickener in cosmetics, and nutritional supplement; inhibitor of lipid-enveloped viruses including herpes simplex.
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BCC5328
Cyromazine
Cyromazine is a triazine insect growth regulator used as an insecticide and an acaricide.
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BCC6252
ML 171
ML171 (2-Acetylphenothiazine;2-APT) is a potent and selective NADPH oxidase 1 (Nox1) inhibitor that blocks Nox1-dependent ROS generation, with an IC50 of 0.25 μM in HEK293-Nox1 confirmatory assay.
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BCN2332
Forskolin
Forskolin (Coleonol) is a potent adenylate cyclase activator with an IC50 of 41 nM and an EC50 of 0.5 μM for type I adenylyl cyclase. Forskolin is also an inducer of intracellular cAMP formation. Forskolin induces differentiation of various cell types and activates pregnane X receptor (PXR) and FXR. Forskolin exerts a inotropic effect on the heart, and has platelet antiaggregatory and antihypertensive actions. Forskolin also induces autophagy.
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BCC3898
MeBIO
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BCC7491
EGTA
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BCC3762
Dicyclomine HCl
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BCC6061
Boc-MLF
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BCC4493
Drospirenone
Drospirenone(Dihydrospirorenone) is a synthetic progestin that is an analog to spironolactone.
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BCC7169
(±)-Blebbistatin
Blebbistatin is a selective non-muscle myosin II (NMII) inhibitor, promotes directional migration of corneal endothelial cells (CECs) and accelerates wound healing, and better preserves cell junctional integrity and barrier function.
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BCC7942
DIDS
Chloride channel blocker; TRPV1 modulator; RAD51 recombinase inhibitor
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BCC7588
Sodium citrate
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BCC5324
Hypoxanthine
Hypoxanthine, a purine derivative, is a potential free radical generator and could be used as an indicator of hypoxia.
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BCC3744
Carbadox
Carbadox is a quinoxaline-di-N-oxide antibiotic compound which is widely fed to nursery-age pigs to control enteric diseases and improve feed efficiency.
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BCC4169
(R)-Oxiracetam
(R)-Oxiracetam is the (R)-enantiomer of the nootropic drug oxiracetam. Oxiracetam (ISF 2522) is a nootropic drug of the racetam family and stimulant.
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BCC4928
Pramiracetam
Pramiracetam is a nootropic drug derived from piracetam, and is more potent. Pramiracetam reportedly improved cognitive deficits associated with traumatic brain injuries.
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BCC6843
Cilostamide
Cilostamide is a selective and potent PDE3 inhibitor, with IC50s of 27 nM and 50 nM for PDE3A and PDE3B, respectively, and has antithrombotic and anti-intimal hyperplastic activity.
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BCC6062
GSK 264220A
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BCC3845
Pridinol Methanesulfonate
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BCC7940
BC 11-38
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BCC3810
Mepiroxol
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BCC8028
BIS-TRIS
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BCC8030
L-Glutathione Reduced
L-Glutathione reduced (GSH; γ-L-Glutamyl-L-cysteinyl-glycine) is an endogenous antioxidant and is capable of scavenging oxygen-derived free radicals.
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BCC5318
Indole-3-carbinol
Indole-3-carbinol (I3C) inhibits NF-κB activity and also is an Aryl hydrocarbon receptor (AhR) agonist, and an inhibitor of WWP1 (WW domain-containing ubiquitin E3 ligase 1).
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BCC7565
Pertussis Toxin
Pertussis Toxin is a protein-based AB5-type exotoxin produced by the bacterium Bordetella pertussis, which causes whooping cough.
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BCC7275
NS 3763
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BCC5660
Flurofamide
Flurofamide is a potent bacterial urease inhibitor with potential in the treatment of infection induced urinary stones.
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BCC5342
FPH1 (BRD-6125)
FPH1 (BRD-6125) is a small molecule, which promotes expansion of iPS-derived hepatocytes.
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BCC5628
Chlorothiazide Sodium
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BCN3828
Troxerutin
Troxerutin, also known as vitamin P4, is a tri-hydroxyethylated derivative of natural bioflavonoid rutins which can inhibit the production of reactive oxygen species (ROS) and depress ER stress-mediated NOD activation.
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BCC4874
TTNPB (Arotinoid Acid)
TTNPB is a highly potent RAR agonist. Competitive binding assays using human RARs yield IC50s of α=5.1 nM, β= 4.5 nM, and γ=9.3 nM, respectively.
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BCC7964
Borrelidin
Borrelidin (Treponemycin) is a bacterial and eukaryal threonyl-tRNA synthetase inhibitor which is a nitrile-containing macrolide antibiotic isolated from Streptomyces rochei. Borrelidin (Treponemycin) is an inhibitor of Cdc28/Cln2 of the budding yeast, with an IC50 of 24 μM. Borrelidin (Treponemycin) is a potent angiogenesis inhibitor, with an IC50 of 0.8 nM, and induces apoptosis of the tube-forming cells. Borrelidin (Treponemycin) has strong antimalarial activities, with IC50s of 1.9 nM and 1.8 nM against K1 and FCR3 strains of Plasmodium falciparum.
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BCC6350
ProINDY
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BCC3897
6,2',4'-Trimethoxyflavone
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BCC4929
Prilocaine
Prilocaine is an amino amide type compound that used for anesthesia.
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BCC1007
b-Casomorphin (1-3)
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BCC5187
Miglustat
Miglustat(OGT918) is an inhibitor of glucosylceramide synthase, primarily to treat Type I Gaucher disease (GD1).
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BCC7602
Swainsonine
Swainsonine is an alkaloid isolated from Astragalus, acts as an inhibitor of α-mannosidase, with anti-tumor activity.
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BCC1477
CHIR-090
CHIR-090 is a potent, slow, tight-binding inhibitor of the LpxC deacetylase. It binds to E. coli LpxC with a Ki of 4.0 nM.
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BCN2196
Melatonin
Melatonin is a hormone made by the pineal gland that can activates melatonin receptor. Melatonin plays a role in sleep and possesses important antioxidative and anti-inflammatory properties. Melatonin is a novel selective ATF-6 inhibitor and induces human hepatoma cell apoptosis through COX-2 downregulation.
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BCC6995
1-Deoxymannojirimycin hydrochloride
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BCC7590
HEPES
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BCC6770
3-Bromo-7-nitroindazole
3-Bromo-7-nitroindazole is a more potent and selective inhibitor of neuronal nitric oxide synthase (nNOS) than eNOS or inducible nitric oxide synthase (iNOS). 3-Bromo-7-nitroindazole affects the intercellular messenger nitric oxide (NO) synthesis throughout the body and brain.
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BCC5689
p-Chlorophenylalanine
Fenclonine is a pharmaceutical intermediate.
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BCC7581
Potassium Chloride
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BCC7255
UBP 296
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BCC7256
UBP 302
UBP 302 is a potent and selective GLUK5-subunit containing kainate receptor antagonist (apparent Kd=402 nM), and displays very little affinity on GluK2 (GluR6) kainate receptors. Anxiolytic effects.
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BCC1810
Nuclear yellow
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BCC5560
Hydroxychloroquine Sulfate
Hydroxychloroquine sulfate (HCQ sulfate) is a synthetic antimalarial drug which can also inhibit Toll-like receptor 7/9 (TLR7/9) signaling.
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BCC6185
2-((1,1-Dioxidotetrahydrothiophen-3-yl)(methyl)amino)-2-oxoethyl 3-(3-nitrophenyl)acrylate
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BCC7591
HEPES Sodium salt
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BCC7585
Sodium phosphate dibasic
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BCC8033
Sodium phosphate monobasic
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BCN4306
(-)-Usnic acid
(+)-Usnic acid is isolated from isolated from lichens, binds at the ATP-binding pocket of mTOR, and inhibits mTORC1/2 activity. (+)-Usnic acid inhibits the phosphorylation of mTOR downstream effectors: Akt (Ser473), 4EBP1, S6K, induces autophay, with anti-cancer activity.
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BCC3871
Triamcinolone Acetonide
Triamcinolone acetonide is a more potent type of triamcinolone, being about 8 times as effective as prednisone.
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BCC3809
Mepenzolate Bromide
Mepenzolate Bromide is a muscarinic antagonist used to treat gastrointestinal disorders, decreases the severity of elastase-induced airspace enlargement and respiratory dysfunction.
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BCC7830
Latrunculin A
Latrunculin A (LAT-A) is a toxin isolated from the red sea sponge Latrunculia magnifica, binds to actin monomers, inhibits polymerization of actin, with Kds of 0.1, 0.4, 4.7 μM and 0.19 μM for ATP-actin, ADP-Pi-actin, ADP-actin and G-actin, respectively.
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BCC7580
Sodium chloride
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BCC7531
RU 26752
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BCC7146
RU 28318, potassium salt
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BCC1144
Pyronaridine Tetraphosphate
Pyronaridine tetraphosphate is a Mannich base anti-malarial with demonstrated efficacy against drug resistant Plasmodium falciparum, P. vivax, P. ovale and P. malariae.
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BCC7377
Triacsin C
Triacsin C (WS 1228A), a natural intracellular long-chain acyl-CoA synthetases (ACSL) inhibitor, is from Streptomyces aureofaciens. Triacsin C inhibits TAG accumulation into lipid droplets (LD) by suppressing ACSL activity. Triacsin C is found to be highly effective against rotavirus replication.
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BCC5171
TPT-260
TPT-260(TPU260) is a thiophene thiourea derivative with molecule weight 260.00 in free base form; There is no formal name yet, we temporally call this molecule as TPT-260.
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BCN5374
Citric acid
Citric acid is a weak organic tricarboxylic acid found in citrus fruits. Citric acid is a natural preservative and food tartness enhancer.
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BCC4164
Gadobutrol
Gadobutrol (Gd-DO3A-butrol; ZK 135079) is a nonionic, paramagnetic contrast agent developed for tissue contrast enhancement in magnetic resonance imaging (MRI).
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BCC1859
Phenylpiracetam
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BCC1797
Nestoron
Nestoron (Elcometrine) is a 19-norprogesterone derivative with high affinity and selectivity for progesterone receptors. Nestoron is a highly selective and potent progestogen that can be used as a hormonal contraceptive.
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BCC7155
Enoximone
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BCC7583
Potassium phosphate monobasic
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BCC6692
MMPX
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BCC6645
MY-5445
MY-5445 is a specific phosphodiesterase type 5 (PDE5) inhibitor. MY-5445 selectively inhibits cGMP PDE with a Ki of 1.3 μM.
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BCC7333
Trequinsin hydrochloride
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BCC1314
7-Epi 10-Desacetyl Paclitaxel
7-Epi 10-desacetyl paclitaxel (7-epi-10-deacetyltaxol), a taxol derivative, exhibits cytotoxicity against HeLa cells with an IC50 of 85 μM.
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BCC4863
Terbinafine HCl
Terbinafine hydrochloride (TDT 067 hydrochloride) is an antifungal medication used to treat fungal infections. It is a potent non-competitive inhibitor of squalene epoxidase from Candida with a Ki of 30 nM. Terbinafine hydrochloride also antibacterial activity against certain Gram-positive and Gram-negative bacteria.
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BCC2559
Cyclosporine
Cyclosporine is a calcineurin phosphatase pathway inhibitor, used as an immunosuppressant drug to prevent rejection in organ transplantation.
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BCC6289
SA 47
SA 47 is a selective and potent inhibitor of fatty acid amide hydrolase (FAAH) and carbamate.
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BCC6240
PBP 10
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BCC4792
Levonorgestrel
Levonorgestrel is a synthetic progestogen used as an active ingredient in some hormonal contraceptives.
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BCC6783
Castanospermine
Castanospermine inhibits all forms of α- and β-glucosidases, especially glucosidase l (required for glucoprotein processing by transfer of mannose and glucose from asparagine-linked lipids).
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BCC3746
Casanthranol
Casanthranol is a concentrated mixture of anthranol glycosides from cascara sagrada (dried bark of Rhamnus p.) and used as a laxative in constipation and various medical conditions, stimulant laxative Casanthranol encourages bowel movements by acting on the intestinal wall to increase muscle contractions.
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BCN5978
Stevenleaf
Gynostemma Extract (Ginsenoside C-Mx1) is a natural product.
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BCC5320
Sapogenins Glycosides
Saponins are a class of chemical compounds of glycosides found in particular abundance in various plant species. In plants, saponins may serve as anti-feedants, and to protect the plant against microbes and fungi.
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BCC4614
Racecadotril
Racecadotril (acetorphan), a potent enkephalinase inhibitor (IC50= 4.5 uM), protects endogenous enkephalins from degradation.
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BCC7752
N-Nonyldeoxynojirimycin
N-Nonyldeoxynojirimycin (NN-DNJ) is a potent inhibitor of alpha-glucosidase and alpha-1,6-glucosidase (IC50s, 0.42, 8.4 μM, respectively), inhibits glycogen breakdown.
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BCC5046
Atomoxetine HCl
Atomoxetine hydrochloride is a potent and selective noradrenalin re-uptake inhibitor (Ki values are 5, 77 and 1451 nM for inhibition of radioligand binding to human NET, SERT and DAT respectively).
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BCC7248
CI 898 trihydrochloride
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BCC4084
Tolrestat
Tolrestat is a potent, orally active aldose reductase inhibitor with IC50 of 35 nM.