others
Products for others
- Reagents(34)
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- Cat.No. Product Name Information
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BCC1546
Elacridar
Elacridar is a potent P-glycoprotein (Pgp) and BCRP inhibitor.
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BCC1547
Elacridar hydrochloride
Elacridar hydrochloride (GF120918A) is a P-glycoprotein inhibitor, and has been used both in vitro and in vivo as a tool inhibitor of P-glycoprotein (Pgp) to investigate the role of transporters in the disposition of various test molecules.
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BCC5493
CB-839
Telaglenastat (CB-839) is a first-in-class, selective, reversible and orally active glutaminase 1 (GLS1) inhibitor. Telaglenastat selectively inhibits GLS1 splice variants KGA (kidney-type glutaminase) and GAC (glutaminase C) compared to GLS2. The IC50s are 23 nM and 28 nM for endogenous glutaminase in mouse kidney and brain, respectively. Telaglenastat inudces autophagy and has antitumor activity.
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BCC7584
Sodium bicarbonate
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BCC6215
Piclamilast
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BCC2556
Febuxostat
Febuxostat(TEI 6720;TMX 67 ) is selective xanthine oxidase inhibitor with Ki of 0.6 nM.
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BCC5601
CCG 203971
CCG-203971 is a second-generation Rho/MRTF/SRF pathway inhibitor. CCG-203971 potently targets RhoA/C-activated SRE-luciferase (IC50 =6.4 μM). CCG-203971 inhibits PC-3 cell migration with an IC50 of 4.2 μM. Potential anti-metastasis Agent.
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BCC4072
K145 hydrochloride
K145 hydrochloride is a selective, substrate-competitive and orally active SphK2 inhibitor with an IC50 of 4.3 µM and a Ki of 6.4 µM. K145 hydrochloride is inactive against SphK1 and other protein kinases. K145 hydrochloride induces cell apoptosis and has potently antitumor activity.
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BCC7058
D-myo-Inositol-1,3,4,5-tetrakisphosphate, octapotassium salt
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BCC5343
MSDC-0160
MSDC 0160 (Mitoglitazone) is a mitochondrial target of thiazolidinediones (mTOT)-modulating insulin sensitizer and a modulator of mitochondrial pyruvate carrier (MPC). MSDC 0160 is a thiazolidinedione (TZD) with antidiabetic and neuroprotective activities. MSDC 0160 has the potential for Alzheimer′s disease.
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BCC5196
R-(-)-Deprenyl hydrochloride
R-(-)-Deprenyl Hydrochloride is a selective inhibitor of monoamine oxidase B (MAO-B).
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BCC7681
SR 11237
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BCC5104
Atglistatin
Atglistatin is a selective adipose triglyceride lipase (ATGL) inhibitor which inhibits lipolysis with an IC50 of 0.7 μM in vitro.
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BCC1766
MK591
Quiflapon sodium (MK-591 sodium) is a selective and specific 5-Lipoxygenase-activating protein (FLAP) inhibitor. Quiflapon sodium is an orally active Leukotriene biosynthesis inhibitor. Induces apoptosis.
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BCC3900
DiMNF
Selective aryl hydrocarbon receptor modulator (SAhRM)
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BCC4787
ID-8
ID-8 is a DYRK inhibitor, and sustains embryonic stem cell self-renewal in long-term culture.
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BCC3868
Thiabendazole
Thiabendazole inhibites the mitochondrial helminth-specific enzyme, fumarate reductase, with anthelminthic property.
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BCC6789
Carboxy-PTIO, potassium salt
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BCC3739
Bismuth Subsalicylate
Bismuth Subsalicylate is the active ingredient in Pepto-Bismol and inhibits prostaglandin G/H Synthase 1/2.
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BCC4876
UNC2250
UNC2250 is a potent and selective Mer inhibitor with an IC50 of 1.7 nM, about 160- and 60-fold selectivity over the closely related kinases Axl/Tyro3.
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BCC5706
L-NIL hydrochloride
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BCC2003
Tirofiban hydrochloride monohydrate
Tirofiban hydrochloride monohydrate is a potent non-peptide, glycoprotein IIb/IIIa (integrins alphaIIbbetaIII) antagonist IC50 value: Target: integrin IIb/IIIa Tirofiban hydrochloride monohydrate blocks platelet aggregation and thrombus formation.
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BCC5197
Zaleplon
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BCC5382
XEN445
XEN445 is a potent and selective EL inhibitor(IC50=0.237 uM), that showed good ADME and PK properties, and demonstrated in vivo efficacy in raising plasma HDLc concentrations in mice.
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BCC5825
Ac2-26
Ac2-26, an active N-terminal peptide of annexin A1 (AnxA1), attenuates ischemia-reperfusion-induced acute lung injury. Ac2-26 also decreases AnxA1 protein expression, inhibits the activation of NF-κB and MAPK pathways in the injured lung tissue.
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BCC7645
RS 25344 hydrochloride
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BCC5411
7-Epi-docetaxel
7-Epi-10-oxo-docetaxel (Docetaxel Impurity C; 7-Epitaxotere) is a impurity of docetaxel.
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BCC6173
Carbazeran citrate
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BCC4048
2-Deoxy-D-glucose
2-Deoxy-D-glucose is a glucose analog that acts as a competitive inhibitor of glucose metabolism, inhibiting glycolysis via its actions on hexokinase.
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BCC6775
Zinc protoporphyrin IX
Zinc Protoporphyrin (Zn(II)-protoporphyrin IX) is an orally active and competitive heme oxygenase-1 (HO-1) inhibitor and markedly attenuates the protective effects of Phloroglucinol (PG) against H2O2. Zinc Protoporphyrin is used as a screening marker of iron deficiency in individual pregnant women and children, but also to assess population iron status in combination with haemoglobin concentration. Zinc Protoporphyrin has anti-cancer activity.
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BCC6342
SB 204990
SB 204990 is a potent and specific inhibitor of ATP citrate lyase (ACLY) enzyme.
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BCC7768
Stauprimide
Stauprimide is a staurosporine analog that promotes embryonic stem cell (ESC) differentiation. Stauprimide is a non-broad spectrum inhibitor that binds to the MYC transcription factor NME2 and blocks its nuclear localization in ESCs, which results in down-regulation of MYC transcription.
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BCC8027
LL 37
LL-37, Human is a 37-residue, amphipathic, cathelicidin-derived antimicrobial peptide, which exhibits a broad spectrum of antimicrobial activity. LL-37, Human could help protect the cornea from infection and modulates wound healing.
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BCC1788
NB-598 Maleate
NB-598 Maleate is a potent and competitive inhibitor of squalene epoxidase (SE), and suppresses triglyceride biosynthesis through the farnesol pathway.
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BCC7242
LE 135
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BCC5189
Travoprost
Travoprost is used to treat glaucoma and ocular hypertension.
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BCC5425
BTS
BTS is a potent inhibitor of Ca2+-stimulated myosin S1 ATPase (IC50 ~ 5 μM) and reversibly blocks the gliding motility.
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BCC5533
Chitinase-IN-1
Chitinase-IN-1 is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50 uM/20 uM compound concentration's inhibitory percentage are 75%/67% for chitinase/N- acetyl-hexosaminidase respectively.
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BCC5534
Chitinase-IN-2
Chitinase-IN-2 is a insect chitinase and N- acetyl hexosaminidase inhibitor and pesticide; 50 uM/20uM compound concentration's inhibitory percentage are 98%/92% for chitinase/N- acetyl-hexosaminidase respectively.
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BCC1824
ortho-iodoHoechst 33258
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BCC1739
meta-iodoHoechst 33258
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BCC1838
para-iodoHoechst 33258
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BCC8073
Pyraclonil
Pyraclonil is a herbicide agent.
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BCC4028
Mc-Val-Cit-PABC-PNP
Mc-Val-Cit-PABC-PNP is a cathepsin cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs).
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BCC6862
2-Iminopiperidine hydrochloride
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BCC2063
X-NeuNAc
X-Neu5Ac is a substrate for chromogenic assay of neuraminidase activity in bacterial expression systems; with a Km of 0.89 mM for neuraminidase.
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BCC3983
SR-9243
SR9243 is a liver-X-receptor (LXR) inverse agonist that induces LXR-corepressor interaction.
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BCC5674
7-NINA
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BCC5545
Ro 48-8071
Ro 48-8071 is an inhibitor of OSC(Oxidosqualene cyclase; IC50=6.5 nM) that has low-density lipoprotein (LDL) cholesterol lowering activity.
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BCC5948
SC 58125
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BCC1095
Dimesna
Dimesna is an protective agent used to decrease urotoxicity.
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BCC8012
SynaptoRedTM C2
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BCC7814
CDP 840 hydrochloride
Potent and selective PDE4 inhibitor
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BCC6036
AT 56
L-PGDS inhibitor
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BCC7703
HQL 79
HQL-79 is a potent, selective and orally active human hematopoietic prostaglandin D synthase (H-PGDS) inhibitor, highly selectively inhibits the synthesis of PGD2, and acts as an anti-allergic agent, with a Kd of 0.8 μM and an IC50 of 6 μM. Shows no obvious effect on COX-1, COX-2, m-PGES, or L-PGDS.
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BCC5410
7-Epi-10-oxo-docetaxel
7-Epi-10-oxo-docetaxel (Docetaxel Impurity 2) is a impurity of docetaxel detected by high performance liquid chromatography (HPLC).
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BCC6158
680C91
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BCC5471
Bethoxazin
Bethoxazin(Bethoguard) is a new broad spectrum industrial microbicide with applications in material and coating preservation.
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BCC5522
Auristatin F
Auristatin F is a potent cytotoxin. Auristatin F, a potent microtubule inhibitor and vascular damaging agent (VDA), can be used in antibody-drug conjugates (ADC).
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BCC7149
YM 90709
YM-90709 is a novel antagonist which inhibits the binding of interleukin-5 to interleukin-5 receptor.
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BCC5476
Aldicarb sulfone
Aldicarb sulfone(Temik sulfone) is a carbamate insecticide; is a cholinesterase inhibitor which prevents the breakdown of acetylcholine in the synapse.
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BCC7679
BMS 453
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BCC5409
10-Oxo Docetaxel
10-Oxo Docetaxel (Docetaxel Impurity 1) is a novel taxoid having remarkable anti-tumor properties and a Docetaxel intermediate.
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BCC5470
Benoxafos
Benoxafos (HOE 2910) is an insecticide.
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BCC4955
NXY-059
Disufenton sodium (NXY-059) is the disulfonyl derivative of the neuroprotective spin trap phenylbutynitrone(PBN), both NXY-059, its parent PBN and their hydrolysis/oxidation product MNT are very powerful scavengers of free radicals.
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BCC6869
Tacrine hydrochloride
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BCC7913
TPEN
TPEN is a specific cell-permeable heavy metal chelator.
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BCC3638
Ezatiostat
Ezatiostat (TER199 free base; TLK199) is a tripeptide analog of glutathione and is a selective and orally active glutathione S-transferase P1-1 (GSTP1) inhibitor. Ezatiostat leads to JNK activation by inhibiting GSTP1. Ezatiostat stimulates both lymphocyte production and bone marrow progenitor proliferation. Ezatiostat has the potential for myelodysplastic syndrome (MDS) treatment.
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BCC6071
CD 2314
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BCC7778
CD 2665
CD2665 is a selective RAR-beta/gamma antagonist, with Ki values of 110 nM, 306 nM for RARγ and RARβ, respectively.
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BCC7809
SC 236
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BCC7912
YC 1
Lificiguat binds to the β subunit of soluble guanylyl cyclase(sGC) with Kd of 0.6-1.1 μM in the presence of CO.
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BCC6763
Tetrindole mesylate
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BCC5400
TAPI-1
TAPI-1 is an ADAM17/TACE inhibitor, which blocks shedding of cytokine receptors.
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BCC3743
Calcium Gluceptate
NSC 42196 is an endogenous metabolite.
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BCC5513
FICZ
FICZ is a potent aryl hydrocarbon receptor (AhR) agonist with a Kd of 70 pM.
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BCC7065
SQ 22536
SQ22536 is an effective adenylate cyclase (AC) inhibitor.
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BCC1338
Aliskiren
Aliskiren(CGP 60536) is a direct renin inhibitor with IC50 of 1.5 nM.
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BCC5018
Aliskiren Hemifumarate
Aliskiren hemifumarate(CGP 60536 hemifumarate) is a direct renin inhibitor with IC50 of 1.5 nM.
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BCC5386
Afobazole
Fabomotizole is an anxiolytic drug; produces anxiolytic and neuroprotective effects without any sedative or muscle relaxant actions.
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BCC7945
Phalloidin
Phalloidin is a mushroom-derived toxin which can be used to label F-actin of the cytoskeleton with fluorochrome (λex=495 nm, λem=520 nm).
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BCC2009
Tonabersat
Tonabersat is a gap-junction modulator.
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BCC6542
O4I1
O4I1 is as a potent Oct3/4 inducer.
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BCC1680
KN-92
KN-92 is an inactive derivative of KN-93.
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BCC1630
Hoechst 33342 analog
Hoechst 33342 analog is an anglog of Hoechst 33342, which is a DNA minor groove binder used fluorochrome for visualizing cellular DNA.
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BCC4288
Prilocaine hydrochloride
Prilocaine hydrochloride is an amino amide type compound that used for anesthesia.
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BCC4895
Caspofungin Acetate
Caspofungin Acetate (MK-0991 Acetate) is an antifungal drug, and noncompetitively inhibits 1,3-β-d glucan synthase activity.
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BCC7786
LG 100754
LG100754 (UVI 2112) is a RXR dimers modulater. LG100754 acts as a RXR:RXR homodimer antagonist, but functions as a agonist towards RXR:PPARα and RXR:PPARγ heterodimers. LG100754 is an insulin sensitizer that functions through RXR.
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BCC7929
DLPC
Selective liver receptor homolog-1 (LRH-1) agonist
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BCC5570
Lomitapide
Lomitapide (AEGR-733; BMS-201038) is a potent inhibitor of microsomal triglyceride-transfer protein (MTP) with an IC50 of 8 nM in vitro.
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BCC7204
Guanylin (human)
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BCC2001
Tipiracil hydrochloride
Tipiracil (hydrochloride) is a thymidine phosphorylase inhibitor (TPI), used for cancer research.
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BCC8072
Penthiopyrad
Penthiopyrad(MTF-753) is a carboxamide fungicide used to control a broad spectrum of diseases on large variety of corps; inhibits fungal respiration by binding to mitochondrial respiratory complex II.
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BCC5812
AF 12198
Potent, selective human type I IL-1 receptor antagonist
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BCC7680
BMS 961
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BCC6495
N6-methyladenosine (m6A)
N6-Methyladenosine is the most prevalent internal (non-cap) modification present in the messenger RNA (mRNA) of all higher eukaryotes. N6-Methyladenosine can modifies viral RNAs and has antiviral activities.
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BCC1106
PA-824
Pretomanid (PA-824) is an antibiotic used for the research of multi-drug-resistant tuberculosis affecting the lungs. Pretomanid exhibits a sub-micromolar MIC against M. tuberculosis (MTB). The MIC values of PA-824 against a panel of MTB pan-sensitive and Rifampin mono-resistant clinical isolates range from 0.015 to 0.25 µg/mL.
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BCC7783
ER 50891
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BCC5815
WKYMVM trifluoroacetate salt
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BCC5816
Trp-Lys-Tyr-Met-Val-Met
WKYMVM is a potent N-formyl peptide receptor (FPR1) and FPRL1/2 agonist, also activates several leukocyte effector functions such as chemotaxis, mobilization of complement receptor-3, and activation of the NADPH oxidase.