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)
- Synthases/Synthetases(5)
- Kisspeptin Receptor(4)
- Tachykinin(6)
- Phosphodiesterases(20)
- NAE(2)
- Thymidine phosphorylase(3)
- Neuromedin U Receptors(2)
- SGK(2)
- RARs(6)
- Caged Compounds(3)
- CaM kinase II(3)
- Retinoid X Receptors(9)
- β-Lactamase(1)
- FLAP(4)
- Cyclooxygenase(10)
- Inositol Phosphatases(4)
- GSNOR(1)
- Fatty Acid Amide Hydrolase(5)
- Farnesyl Diphosphate Synthase(1)
- Hexokinase(2)
- Guanylyl Cyclase(7)
- Nuclear Receptors(9)
- BMI-1(1)
- Cytokine(4)
- NADPH Oxidase(2)
- AhR(9)
- Cell Adhesion Molecules(4)
- PI 3-kinase(2)
- 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)
- Nampt(5)
- Nrf2(2)
- nNOS(9)
- Transketolase(1)
- Adenylate cyclase(8)
- Lysophosphatidic Acid Receptors(4)
- Antioxidants(4)
- XAO(3)
- Nitric Oxide(5)
- Glycoprotein(1)
- Oxygenases/Oxidases(3)
- LXR(6)
- GSTP1-1(1)
- β(1,3)-D-Glucan Synthase(2)
- Formyl Peptide Receptors(10)
- Cell Penetrating Peptide(2)
- CPG2(1)
- Neuropeptide FF/AF Receptors(6)
- Reductases(3)
- MGMT(2)
- Glyoxalase I(1)
- CPA(1)
- Collagen proline hydroxylase(2)
- PDHK(1)
- FBPase(1)
- FXR(4)
- Gutathione S-transferase(1)
- Ceramidases(1)
- Guanylate Cyclase(3)
- AT Receptors(1)
- Lp-PLA2(1)
- CERK(1)
- dCTP Pyrophosphatase(1)
- eIF2a(1)
- Aldose reductase(3)
- BCRP(1)
- General Imidazolines(1)
- PGC-1α(1)
- Thrombopoietin Receptor(2)
- IMPDH(1)
- IL Receptor(1)
- Diacylglycerol Kinase(1)
- GLI(1)
- LpxC(1)
- MDR multidrug resistance(1)
- Endopeptidase(1)
- Norepinephrine uptake(1)
- Dihydrofolate Reductase(1)
- MyD88(1)
- COT/TpI2(2)
- sFRP-1(1)
- ATP citrate lyase(1)
- Cat.No. Product Name Information
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BCC7582
Calcium chloride dihydrate
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BCC7592
Boric acid
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BCC7799
FFN 511
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BCC5183
Tirasemtiv
Tirasemtiv is an activator of the fast skeletal muscle troponin complex.
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BCC6301
TC ASK 10
TC ASK 10 (Compound 10) is a potent, selective and orally active apoptosis signal-regulating kinase 1 (ASK1) inhibitor with an IC50 of 14 nM. The inhibitory activities of TC ASK 10 towards other representative panel of kinases are less than 50%, except for ASK2 (IC50 of 0.51 μM).
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BCC5339
Microcystin-LR
Microcystin-LR inhibits protein phosphatase type 1 and type 2A (PP1 and PP2A) activities in the cytoplasm of liver cells.
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BCC7529
Phenserine
Phenserine ((-)-Eseroline phenylcarbamate) is a derivative of Physostigmine and is a potent, noncompetitive, long-acting and selective AChE inhibitor. Phenserine reduces β-amyloid precursor protein (APP) and β-amyloid peptide (Aβ) formation. Phenserine improves cognitive performance and attenuates the progression of Alzheimer's disease.
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BCC2049
VTP-27999 2,2,2-trifluoroacetate
VTP-27999 TFA is an alkyl amine Renin inhibitor; VTP-27999 TFA is useful for Hypertension and End-Organ Diseases.
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BCC1958
sodium 4-pentynoate
sodium 4-pentynoate is a alkynylacetate analogue; can be metabolically incorporated onto cellular proteins through biosynthetic mechanisms for profiling of acetylated proteins in diverse cell types.
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BCC5555
Cyclocytidine HCl
Ancitabine (hydrochloride) is an important antileukemia drugs.
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BCC5373
AM580
AM580 is a selective RARα agonist with IC50 and EC50 of 8 nM and 0.36 nM, respectively.
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BCC6924
AGN 192403 hydrochloride
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BCC7485
Jasplakinolide
Jasplakinolide is a potent actin polymerization inducer and stabilizes pre-existing actin filaments. Jasplakinolide binds to F-actin competitively with phalloidin with a Kd of 15 nM. Jasplakinolide, a naturally occurring cyclic peptide from the marine sponge, has both fungicidal and anti-cancer activity.
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BCC8057
GK921
GK921 is a transglutaminase 2 (TGase) inhibitor with an IC50 of 7.71 μM for human recombinant TGase 2.
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BCC3818
Monobenzone
Monobenzone is a potent skin depigmenting agent. Monobenzone induces depigmentation and active human vitiligo and exhibits good potential for vitiligo research.
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BCC7996
AS 2034178
Selective FFA1 (GPR40) agonist
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BCC5618
UNC 3230
UNC3230 is a potent, selective and ATP-competitive phosphatidylinositol 4-phosphate 5 kinase type 1C (PIP5K1C) inhibitor with an IC50 of ~41 nM. UNC3230 also inhibits PIP4K2C and does not inhibit any of the other lipid kinases. UNC3230 has antinociceptive and anticancer effects.
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BCC7953
PTIQ
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BCC6515
Disodium (R)-2-Hydroxyglutarate
D-alpha-Hydroxyglutaric acid disodium salt is a weak competitive α-Ketoglutarate(α-KG)-dependent dioxygenase inhibitor with Ki of 10.87±1.85 mM. Ki for L-Hydroxyglutaric acid (L-2-HG) is 0.628±0.036 mM.
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BCC2065
YK-4-279
YK 4-279 is an inhibitor of RNA Helicase A (RHA) binding to the oncogenic transciption factor EWS-FLI1.
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BCC7371
Lazabemide hydrochloride
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BCC6177
MitoPY1
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BCC6097
EC 23
EC23 (AGN 190205) is a stable synthetic retinoid analogue and induces neuronal differentiation.
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BCC8075
6-O-α-Maltosyl-β-cyclodextrin
6-O-α-maltosyl-β cyclodextrin (Mal-βCD) is a cellular cholesterol modifier which can form soluble inclusion complex with cholesterol and is much less cytotoxic to human erythrocytes and Caco-2 cells; a cyclodextrin derivative.
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BCC4107
Entacapone sodium salt
Entacapone is a specific, potent, peripherally acting catechol-O-methyltransferase (COMT) inhibitor with IC50 of 151 nM for PD treatment.
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BCC4711
Risedronate
Risedronic acid (Risedronate ) is a pyridinyl biphosphonate which inhibits osteoclast-mediated bone resorption.
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BCC6644
ML 9 hydrochloride
ML-9 is a selective and potent inhibitor of Akt kinase, inhibits myosin light-chain kinase (MLCK) and stromal interaction molecule 1 (STIM1) activity. ML-9 inhibits inhibits MLCK, PKA and PKC activity with Ki values of 4, 32 and 54 μM, respectively. ML-9 induces autophagy by stimulating autophagosome formation and inhibiting their degradation.
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BCC3754
Clinafloxacin CI96 AM1091
Clinafloxacin(PD-127391) is a fluoroquinolone antibiotic.
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BCC1631
Hoechst 33342 analog 2
Hoechst 33342 analog 2 is an anglog of Hoechst 33342, which is a DNA minor groove binder used fluorochrome for visualizing cellular DNA.
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BCC1956
SMND-309
SMND-309 is a metabolite of salvianolic acid B, and exhibits neuroprotective effects in cultured neurons and in permanent middle cerebral artery occlusion rats.
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BCC7739
GYY 4137 morpholine salt
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BCC6824
EIT hydrobromide
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BCC7406
CD 1530
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BCC3776
Epleremone
Eplerenone is an aldosterone antagonist with an IC50 of 0.36 μM.
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BCC7776
TUG 424
TUG-424 is a potent and selective free fatty acid receptor 1 (FFA1/GPR40) agonist with an EC50 of 32 nM. TUG-424 significantly increases glucose-stimulated insulin secretion at 100 nM. TUG-424 may serve to explore the role of FFA1 in metabolic diseases such as diabetes or obesity.
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BCC6189
TC-S 7005
TC-S 7005 is a Polo-like kinases (Plks) inhibitor with IC50s of 4 nM, 24 nM and 214 nM for Plk2, Plk3, and Plk1, respectively.
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BCC4734
4-Hydroxy-Teriflunomide
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BCC6206
Y 11
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BCC7296
FURA-2AM
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BCC7601
Kifunensine
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BCC5211
Ouabain Octahydrate
Ouabain Octahydrate is an inhibitor of Na+/K+-ATPase, used for the treatment of congestive heart failure.
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BCC7678
S 32826
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BCC7241
Ch 55
Ch55 is a potent synthetic retinoid. Ch55 binds to RAR-α and RAR-β receptors with high affinity. Ch55 displays low affinity for cellular retinoic acid binding protein (CRABP). Ch55 is a potent inducer of the differentiation of HL60 cells with an EC50 of 200 nM. Ch55 can be used for cancer research.
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BCC7867
Salermide
Salermide is an inhibitor of Sirt1 and Sirt2; can cause strong cancer-specific apoptotic cell death.
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BCC4799
Metformin HCl
Metformin hydrochloride (1,1-Dimethylbiguanide hydrochloride) inhibits the mitochondrial respiratory chain in the liver, leading to activation of AMPK, enhancing insulin sensitivity for type 2 diabetes research. Metformin hydrochloride triggers autophagy.
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BCC8035
BRD 7552
BRD7552 is an inducer of transcription factor PDX1, which increases insulin expression.
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BCC6669
N1,N12-Diethylspermine tetrahydrochloride
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BCC5204
Ibandronic acid
Ibandronic acid is a highly potent nitrogen-containing bisphosphonate used for the treatment of osteoporosis.
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BCC5326
Guanosine Hydrate
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BCC1857
PF-8380
PF-8380 is a potent autotaxin inhibitor with an IC50 of 2.8 nM in isolated enzyme assay and 101 nM in human whole blood.
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BCC6077
Kisspeptin 234
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BCC8029
Bromophenol Blue
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BCC6630
Ambenonium dichloride
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BCC5858
Antagonist G
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BCC7775
A 1120
A 1120, a nonretinoid retinol-binding protein 4 (RBP4) antagonist, has a high affinity with the Ki value of 8.3 nM, which disrupts the interaction between RBP4 and its binding partner transthyretin.
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BCC6954
Siguazodan
Siguazodan (SKF 94836) is a potent, selective and orally active phosphodiesterase III (PDE-III) inhibitor with an IC50 of 117 nM. Siguazodan increases cAMP accumulation in intact platelets with an EC50 of 18.88 μM. Siguazodan also inhibits phenylephrine-induced 5-HT release with an IC50 value of 4.2 μM.
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BCC2501
Risedronate Sodium
Risedronate sodium is a pyridinyl biphosphonate which inhibits osteoclast-mediated bone resorption.
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BCC5475
Aldicarb
Aldicarb(OMS771; UC-21149) is a carbamate insecticide; is a cholinesterase inhibitor which prevents the breakdown of acetylcholine in the synapse.
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BCC1773
MLN4924 HCl salt
Pevonedistat hydrochloride (MLN4924 hydrochloride) is a potent and selective NEDD8-activating enzyme (NAE) inhibitor, with an IC50 of 4.7 nM.
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BCC5466
Novaluron
Novaluron is a chemical with pesticide properties, belonging to the class of insecticides called insect growth regulators.
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BCC6349
INDY
INDY is a potent and ATP-competitive Dyrk1A and Dyrk1B inhibitor with IC50s of 0.24 μM and 0.23 μM, respectively. INDY binds in the ATP pocket of the enzyme and has a Ki value of 0.18 μM for Dyrk1A. INDY sharply reduces the self-renewal capacity of normal and tumorigenic cells in primary Glioblastoma (GBM) cell lines and neural progenitor cells.
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BCC5969
BCECF-AM
BCECF-AM is a cell membrane permeable compound, widely used as a fluorescent indicator for intracellular pH.
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BCC5847
Neuromedin U (rat)
Neuromedin U, rat is a 23-amino acid brain-gut peptide. Neuromedin U (NMU), through its cognate receptor NMUR2 in the central nervous system, regulates several important physiological functions, including energy balance, stress response, and nociception.
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BCC7195
(R)-(+)-Blebbistatin
(+)-Blebbistatin is the inactive enantiomer of (–)-Blebbistatin. (–)-Blebbistatin is a selective inhibitor of myosin II ATPase.
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BCC1551
EMD638683
EMD638683 is a highly selective SGK1 inhibitor, with an IC50 value of 3 μM.
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BCC2540
Tazarotene
Tazarotene (AGN 190168) is a selective retinoic acid receptor (RAR) agonist for the treatment of plaque psoriasis and acne vulgaris.
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BCC7589
TRIS hydrochloride
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BCC6936
BU 226 hydrochloride
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BCC7698
NPE-caged-proton
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BCC6121
TMN 355
TMN355 is a potent chemical cyclophilin A inhibitor and reduces foam cell formation and cytokine secretion. TMN355 is used for atherosclerosis.
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BCC5638
KN-93 Phosphate
KN-93 Phosphate is a potent and specific inhibitor of Ca2+/calmodulin-dependent protein kinase II (CaMKII) with Ki of 0.37 μM, no remarkable inhibitory effects on APK, PKC, MLCK or Ca2+-PDE activities.
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BCC6110
Fluorobexarotene
Fluorobexarotene (compound 20) is a potent retinoid-X-receptor (RXR) agonist, with a Ki value of 12 nM and an EC50 value of 43 nM for RXRα receptor. Fluorobexarotene possesses an apparent RXR binding affinity that is 75% greater than Bexarotene.
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BCC1384
Avibactam
Avibactam free acid (NXL-104 free acid) is a covalent and reversible non-β-lactam β-lactamase inhibitor which inhibits β-lactamase TEM-1 and CTX-M-15 with IC50s of 8 nM and 5 nM, respectively.
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BCC7858
PE 154
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BCC5588
GSK2190915 sodium salt
Fiboflapon sodium (GSK2190915; AM-803) is a potent and orally bioavailable 5-lipoxygenase-activating protein (FLAP) inhibitor with a potency of 2.9 nM in FLAP binding, an IC50 of 76 nM for inhibition of LTB4 in human blood.
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BCN2710
Tranexamic acid
Tranexamic acid (Transamin) is an antifibrinolytic for blocking lysine-binding sites of plasmin and elastase-derived plasminogen fragments with IC50 of 5 mM.
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BCC4195
TGR5 Receptor Agonist
TGR5 Receptor Agonist (CCDC), a potent TGR5(GPCR19) agonist, shows improved potency in the U2-OS cell assay (pEC50=6.8) and in melanophore cells (pEC50=7.5).
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BCC6336
Peroxy Orange 1
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BCC7419
Tenidap
Tenidap, a non-steroidal anti-inflammatory drug, is a selective COX-1 inhibitor, with IC50 values of 0.03 µM and 1.2 µM for COX-1 and COX-2, respectively. Tenidap has anti-inflammatory and antirheumatic properties. Tenidap is also a specific SLC26A3 inhibitor.
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BCC4287
Dorzolamide
Dorzolamide(L671152; MK507) is an anti-glaucoma agent, which is a carbonic anhydrase inhibitor.
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BCC7762
AS 1949490
AS1949490 is a potent and selective SHIP-2 (SH2 domain-containing inositol 5′ phosphatase 2) inhibitor, with an IC50 of 620 nM. AS1949490 activated glucose metabolism via up-regulation of GLUT1 gene in L6 myotubes.
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BCC7974
TC Mps1 12
TC-Mps1-12 is a potent and selective monopolar spindle 1 (Mps1) inhibitor, with an IC50 of 6.4 nM.
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BCC1354
AM679
AM679 is a potent and selective FLAP inhibitor with IC50s of 2.2 nM/0.6 nM/154 nM for FLAP binding/hLA/hWB respectively.
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BCC8059
NVS-CRF38
NVS-CRF38 is a novel corticotropin-releasing factor receptor 1 (CRF1) antagonist with low water solubility.
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BCC5530
CaMKII-IN-1
CaMKII-IN-1 is a potent and highly selective CaMKII inhibitor with IC50 of 63 nM; significantly high selectivity against CaMKIV, MLCK, p38a, Akt1, and PKC.
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BCC1677
Ketone Ester
BD-AcAc 2, added in diet, could elevated mean blood ketone bodies of 3.5 mm and lowered plasma glucose, insulin, and leptin in animals; ketone ester given orally would delay CNS-OT seizures in rats breathing hyperbaric oxygen.
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BCC4127
N6022
N6022 is a selective, and reversible inhibitor of S-nitrosoglutathione reductase (GSNOR) with IC50 of 8 nM and Ki of 2.5 nM. Phase 1/2.
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BCN2605
Vanillin
Vanillin (p-Vanillin) is a single molecule extracted from vanilla beans and also a popular odor used widely in perfume, food and medicine.
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BCC7051
(-)-Terreic acid
Selective inhibitor of BTK
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BCC7966
JZL 195
JZL195 is a selective and efficacious dual fatty acid amide hydrolase (FAAH) and monoacylglycerol lipase (MAGL) inhibitor with IC50s of 2 and 4 nM, respectively.
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BCC4885
Alendronate
Alendronate (sodium hydrate) is a farnesyl diphosphate synthase inhibitor with IC50 of 460 nM.
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BCC8094
PF-04991532
PF-04991532 is a potent, hepatoselective glucokinase activator with EC50s of 80 and 100 nM in human and rat, respectively.
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BCC5924
CFM 1571 hydrochloride
Soluble guanylyl cyclase (sGC) activator
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BCC2027
Valspodar
Valspodar is a selective P-glycoprotein inhibitor that has been used as an experimental cancer treatment and chemosensitizer.
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BCC7506
BYK 191023 dihydrochloride
Potent and selective inhibitor of iNOS
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BCC7741
GSK 4112
GSK4112 is a Rev-erbα agonist with EC50 of 0.4 μM, also is a small molecule chemical probe for the cell biology of the nuclear heme receptor Rev-erbα.
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BCC5640
PTC209 HBr
PTC-209 hydrobromide is a specific BMI-1 inhibitor with IC50 of 0.5 μM in both GEMS reporter and ELISA assays.
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BCC5668
BU 239 hydrochloride
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BCC5939
A 350619 hydrochloride
Soluble guanylyl cyclase (sGC) activator
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BCC5813
Ro 26-4550 trifluoroacetate