others
Products for others
- Reagents(34)
- Fluorescent Probes(8)
- Others(296)
- ASK1(1)
- Cholinesterases(11)
- Renin(5)
- RAR/RXR(8)
- Imidazoline Receptors(6)
- Actin(9)
- Free Fatty Acid Receptors(6)
- Matrix Metalloprotease(1)
- ES-FLI1/RHA(1)
- Heme oxygenase(7)
- Retinoic Acid Receptors(16)
- COMT(2)
- Myosin(6)
- DNA Stain(20)
- Miscellaneous Compounds(9)
- iNOS(10)
- Mineralocorticoid Receptor(4)
- Polo-like Kinase(2)
- Focal Adhesion Kinase(2)
- Glycosylases(5)
- Autotaxin(3)
- Sir2-like Family Deacetylases(2)
- Transcription Factors(8)
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- Guanylyl Cyclase(7)
- Nuclear Receptors(9)
- BMI-1(1)
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- Natriuretic Peptide Receptors(4)
- Pregnane X Receptors(1)
- Progesterone Receptor(10)
- Menin-MLL(2)
- SPHK(3)
- Squalene epoxidase(5)
- Kainate Receptors(12)
- Arginase(1)
- Hydroxylases(7)
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- Cat.No. Product Name Information
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BCC5023
Abacavir sulfate
Abacavir sulfate (ABC) is a powerful nucleoside analog reverse transcriptase inhibitor (NRTI) used to treat HIV and AIDS.
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BCC1741
Methylproamine
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BCC7111
SC 560
SC-560 is a potent and selective COX-1 inhibitor with an IC50 of 9 nM.
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BCC6082
HX 531
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BCC6083
HX 630
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BCC1532
DMA
DMA is a fluorescent compound (λex=340 nm, λem=478 nm).
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BCC5546
Ro 48-8071 fumarate
Ro 48-8071 fumarate is an inhibitor of OSC (Oxidosqualene cyclase) with IC50 of appr 6.5 nM.
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BCC7549
Mesopram
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BCC7190
YM 976
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BCC5419
AGN 195183
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BCC4417
HIV-1 Tat Protein Peptide
TAT (YGRKKRRQRRR) is derived from the transactivator of transcription (TAT) of human immunodeficiency virus-1 (HIV-1) and is a cell-penetrating peptide. TAT can increase the yields and the solubility of heterologous proteins.
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BCC1452
Carboxypeptidase G2 (CPG2) Inhibitor
Carboxypeptidase G2 (CPG2) Inhibitor is a novel Carboxypeptidase G2 (CPG2) Inhibitor, Antitumor agents.
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BCC5854
Neuropeptide AF (human)
Neuropeptide AF (93-110), Human is an endogenous antiopioid peptide.
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BCC5829
Neuropeptide SF (human)
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BCC6102
ES 936
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BCC6214
TAS 301
TAS-301 is an inhibitor of smooth muscle cell migration and proliferation, and inhibits PKC activation induced by PDGF.
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BCC6795
Aminoguanidine hydrochloride
Aminoguanidine hydrochloride is a diamine oxidase and NO synthase inhibitor, reduces levels of advanced glycation end products (AGEs) through interacting with 3-deoxyglucosone, is an investigational drug for the treatment of diabetic nephropathy.
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BCC3870
Tiopronin (Thiola)
Tiopronin is a prescription thiol drug used to control the rate of cystine precipitation and excretion in the disease cystinuria.
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BCC5361
AP1903
Rimiducid (AP1903) is a dimerizer agent that acts by cross-linking the FKBP domains. Rimiducid (AP1903) dimerizes the Caspase 9 suicide switch and rapidly induces apoptosis.
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BCC3840
Piromidic Acid
Piromidic acid is a quinolone antibiotic.
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BCC5469
Athidathion
Athidathion(GS-13006) is an organophosphate insecticide.
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BCC7637
CD 3254
CD3254 a potent and selective retinoid-X-receptor (RXR) agonist.
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BCC3811
Mesna
Mesna, is a synthetic small molecule, widely used as a systemic protective agent against chemotherapy toxicity, but is primarily used to reduce hemorrhagic cystitis induced by cyclophosphamide.
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BCC5852
MLCK inhibitor peptide
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BCC6485
O6-Benzylguanine
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BCC7619
Ro 61-8048
Ro 61-8048 is a potent and selective inhibitors of kynurenine hydroxylase with IC50 of 37 nM.
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BCC6527
GMX1778 (CHS828)
CHS-828 (GMX1778) is a competitive inhibitor of nicotinamide phosphoribosyltransferase (NAMPT), with an IC50 less than 25 nM. CHS-828 (GMX1778) exerts a cytotoxic effect by decreasing the cellular level of NAD+ and exhibits a potent anticancer activity.
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BCC1980
Talarozole
Talarozole (R115866) is an oral systemic all-trans retinoic acid metabolism blocking agent (RAMBA) which increases intracellular levels of endogenous all-trans retinoic acid (RA). Talarozole inhibits both CYP26A1 and CYP26B1 with IC50s of 5.4 and 0.46 nM, respectively.
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BCC5463
PNU-159682
PNU-159682, a highly potent metabolite of the anthracycline nemorubicin (DNA topoisomerase II inhibitor) with outstanding cytotoxicity, is a potent ADCs cytotoxin.
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BCC5682
RS 45041-190 hydrochloride
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BCC6212
NS 2028
NS-2028 is a highly selective soluble Guanylyl Cyclase (sGC) inhibitor with IC50 values of 30 nM and 200 nM for basal and NO-stimulated enzyme activity. NS-2028 inhibits soluble Guanylyl Cyclase activity in homogenates of mouse cerebellum and neuronal NO synthase with IC50 values of 17 nM and 20 nM. NS-2028 inhibits 3-morpholino-sydnonimine (SIN-1)-elicited formation of cyclic GMP in human cultured umbilical vein endothelial cells with an IC50 of 30 nM. NS-2028 is commonly used in the research of nitric oxide signaling pathways, it inhibits NO-dependent relaxant responses in non-vascular smooth muscle completely (1 μM). NS-2028 reduces vascular endothelial growth factor-induced angiogenesis and permeability.
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BCC6765
BU 224 hydrochloride
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BCC1457
CB30865
CB30865(ZM 242421) is a potent inhibitor of Nampt , an enzyme present in the NAD biosynthetic pathway.
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BCC3835
Pasiniazid
Pasiniazid is an anti-TB and anti-leprosy drug, used to treat various types of TB and leprosy.
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BCC6764
Pirlindole mesylate
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BCC5172
TPT-260 Dihydrochloride
TPT-260 Dihydrochloride (NSC55712) 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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BCC1750
Micafungin sodium
Micafungin sodium (FK 463 sodium) is an antifungal agent which inhibits 1, 3-beta-D-glucan synthesis.
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BCC5186
Miglustat hydrochloride
Miglustat hydrochloride is an inhibitor of glucosylceramide synthase, primarily to treat Type I Gaucher disease (GD1).
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BCC5465
Ipfencarbazone
Ipfencarbazone is a substance being developed for the control of weeds such as watergrass in rice; herbicide agent.
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BCC1798
NG 52
NG 52 (Compound 52 ) is a potent, cell-permeable, reversible, selective, and ATP-compatible inhibitor of the cell cycle-regulating kinase, Cdc28p (IC50 = 7 μM), and the related Pho85p kinase (IC50 = 2 μM).
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BCC3822
Nifenazone
Nifenazone is a pyrazole drug which can be used in the in the treatment of a variety of rheumatic disorders.
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BCC7057
1400W dihydrochloride
1400W dihydrochloride is a potent and selective inhibitor of human inducible NO synthase with Ki values of 7 nM.
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BCC6823
AMT hydrochloride
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BCC7697
BMS 493
BMS493 is an inverse pan-retinoic acid receptor (RAR) agonist. BMS493 increases nuclear corepressor interaction with RARs. BMS493 also could prevent retinoic acid-induced differentiation.
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BCC3736
Betamethasone Valerate
Betamethasone valerate (Betamethasone 17-valerate), the 17-valerate ester of Betamethasone, is a topical corticosteroid with anti-inflammatory activity. Betamethasone valerate is used in the treatment of recurrent aphthous stomatitis. Betamethasone valerate inhibits the binding of the radiolabeled glucocorticoid dexamethasone (3H dexamethasone) to human epidermis and mouse skin with IC50s of 5 and 6 nM, respectively.
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BCC6031
BMS 753
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BCN2951
Sodium Dichloroacetate
Sodium dichloroacetate is a metabolic regulator in cancer cells' mitochondria with anticancer activity. Sodium dichloroacetate inhibits PDHK, resulting in decreased lactic acid in the tumor microenvironment. Sodium dichloroacetate increases reactive oxygen species (ROS) generation and promotes cancer cell apoptosis. Sodium dichloroacetate also works as NKCC inhibitor.
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BCC3844
Potassium Canrenoate
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BCC4165
Oxonic acid potassium salt
Potassium oxonate is an inhibitor of uricase, inhibits the phosphorylation of 5-FU to 5-fluorouridine-5'-monophosphate catalyzed by pyrimidine phosphoribosyl-transferase in a different manner from allopurinol in cell-free extracts and intact cells in vitro.
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BCC1598
Glyoxalase I inhibitor
Glyoxalase I inhibitor is a potent Glyoxalase I inhibitor, candidate for anticancer agents.
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BCN5049
Cytochalasin D
Cytochalasin D (Zygosporin A; NSC 209835) is a potent and cell-permeable inhibitor of actin polymerization derived from fungus, inhibits the G-actin–cofilin interaction by binding to G-actin. Cytochalasin D (Zygosporin A; NSC 209835) also inhibits the binding of cofilin to F-actin and decreases the rate of both actin polymerization and depolymerization in living cells.
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BCC6746
L-Canavanine sulfate
L-Canavanine sulfate is a selective inhibitor of inducible NO synthase.
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BCC5895
Lyn peptide inhibitor
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BCC1500
CPA inhibitor
CPA inhibitor is a potent inhibitor for carboxypeptidase A (CPA).
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BCC8070
Tiadinil
Tiadinil is a plant activator of systemic acquired resistance, boosts the production of herbivore-induced plant volatiles; fungicide.
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BCC1495
Collagen proline hydroxylase inhibitor-1
Collagen proline hydroxylase inhibitor-1 is an antifibroproliferative agents.
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BCC1494
Collagen proline hydroxylase inhibitor
Collagen proline hydroxylase inhibitor is a collagen proline hydroxylase inhibitor; useful for antifibroproliferative agents.
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BCC5319
Sodium Monensin
Monensin sodium salt is an antibiotic secreted by the bacteria Streptomyces cinnamonensis. Monensin sodium salt is an ionophore that mediates Na+/H+ exchange.
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BCC5950
NPE-caged-HPTS
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BCC1415
Benfotiamine
Benfotiamine is a synthetic S-acyl derivative of thiamine (vitamin B1); an antioxidant dietary supplement.
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BCC5828
MLCK inhibitor peptide 18
MLCK inhibitor peptide 18 is a myosin light chain kinase (MLCK) inhibitor with an IC50 of 50 nM, and inhibits CaM kinase II only at 4000-fold higher concentrations.
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BCC5521
Emapunil
Emapunil(AC-5216;XBD-173) is a translocator protein [TSPO (18 kDa)] ligand.
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BCC3779
Famprofazone
Famprofazone is a non-steroidal anti-inflammatory agent (NSAID) of the pyrazolone series, has analgesic, anti-inflammatory, and antipyretic effects.
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BCC5416
AGN 194310
AGN 194310 (VTP-194310) is a high affinity, potent and selective retinioic acid receptors (RARs) pan-antagonist with
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BCC1778
MPTP hydrochloride
MPTP hydrochloride is a brain penetrant dopamine neurotoxin, inducing Parkinson’s Disease. MPTP hydrochloride, a precusor of MPP+, induces apoptosis.
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BCC6054
Neuropeptide SF (mouse, rat)
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BCC1623
Hoechst 33258
Hoechst 33258 trihydrochloride is a fluorescent dyes, which can be used as a cell dye for DNA.
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BCC1629
Hoechst 33342
Hoechst 33342 is a DNA minor groove binder used fluorochrome for visualizing cellular DNA.
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BCC1625
Hoechst 33258 analog 2
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BCC1627
Hoechst 33258 analog 5
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BCC1626
Hoechst 33258 analog 3
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BCC1620
HOE 32020
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BCC1632
Hoechst 34580
Hoechst 34580 is a cell-permeable fluorescent dye for staining DNA and nuclei.
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BCC1621
HOE 32021
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BCC1622
HOE 33187
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BCC3802
Laquinimod (ABR-215062)
Laquinimod is a potent immunomodulator which prevents neurodegeneration and inflammation in the central nervous system.
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BCC4294
AZD7545
AZD7545 is a potent, competitive, selective PDHK2 (pyruvate dehydrogenase kinase 2) inhibitor with IC50s of 36.8 nM, 6.4 nM for PDHK1 and PDHK2, respectively.
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BCC7740
BMS 195614
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BCC7934
Wiskostatin
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BCC6847
TRIM
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BCC6092
AR-C 102222
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BCC5526
Z-Ile-Glu-Pro-Phe-Ome
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BCC8015
Propidium iodide
Propidium iodide is a red-fluorescent dye that can be used to stain cells.
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BCC7932
BAY 41-2272
BAY 41-2272 is a soluble guanylate cyclases (sGC) activator.
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BCC5826
Ac2-12
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BCC5938
KF 38789
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BCC1624
Hoechst 33258 analog
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BCC6535
D-Luciferin
D-luciferin is the natural substrate of luciferases that catalyze the production of light in bioluminescent insects.
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BCC1731
MB05032
MB05032 is a special and efficacious GNG inhibitor targeted the AMP binding site of fructose 1,6-bisphosphatase (FBPase) with an IC50 value of 16 nM.
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BCC5504
ESI-09
ESI-09 is a novel noncyclic nucleotide EPAC antagonist with IC50 values of 3.2 and 1.4 μM for EPAC1 and EPAC2, respectively.
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BCC6037
MMK 1
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BCC5341
FH1(BRD-K4477)
FH1(BRDK4477) is a small molecule that can enhance the functions of cultured hepatocytes.
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BCC7188
ICI 63197
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BCC5184
Tirapazamine
Tirapazamine is an anticancer agent that shows selective cytotoxicity for hypoxic cells in solid tumors, thereby inducing single-and double-strand breaks in DNA, base damage, and cell death.
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BCC7941
MMF
Monomethyl fumarate, an active metabolite of Dimethyl fumarate (DMF), is a potent GPR109A agonist. Monomethyl fumarate has the potential for multiple neuroprotective pathways and other models of retinal disease.
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BCC4001
NH125
NH125 is a potent and selective inhibitor of eukaryotic elongation factor 2 kinase (eEF-2K/CaMKIII), also can induce eEF2 phosphorylation, with an IC50 of 60 nM for eEF-2K.
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BCC4500
GW4064
GW 4064 is a potent FXR agonist with an EC50 of 65 nM.
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BCC8071
Valifenalate
Valifenalate(IR5885; Valiphenal), which is approved for application on high-value crops such as grapes, tomatoes and other vegetables, is effective against various types of mildew and is currently marketed primarily under the Valis moniker; insecticide agent.
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BCC4168
sn-Glycero-3-phosphocholine
sn-Glycero-3-phosphocholine (Choline Alfoscerate) is a precursor in the biosynthesis of brain phospholipids and increases the bioavailability of choline in nervous tissue. sn-Glycero-3-phosphocholine (Choline Alfoscerate) has significant effects on cognitive function with a good safety profile and tolerability, and is effective in the treatment of Alzheimer's disease and dementia.
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BCC5997
Ac9-25