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)
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- Diacylglycerol Kinase(1)
- GLI(1)
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- Endopeptidase(1)
- Norepinephrine uptake(1)
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- COT/TpI2(2)
- sFRP-1(1)
- ATP citrate lyase(1)
- Cat.No. Product Name Information
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BCC5460
GKT137831
Setanaxib (GKT137831) is a selective NADPH oxidase (NOX1/4) inhibitor with Kis of 140 and 110 nM, respectively.
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BCC5446
Aurothioglucose
Aurothioglucose (Gold thioglucose) is a well known active-site inhibitor of TrxR1, inhibited TrxR1 activity in HeLa cell cytosol but had no effect on the viability of the cells.
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BCC5474
Cyhalofop
Cyhalofop(Cyhalofop acid) is a recently registered herbicide from the aryloxyphenoxy propionate group in India to control a wide range of grass weed species at various growth stages in rice crop.
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BCC4284
Acarbose sulfate
Acarbose sulfate is an inhibitor of alpha glucosidase, an anti-diabetic drug.
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BCC6306
ML 202
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BCC3637
StemRegenin 1 (SR1)
StemRegenin 1 is a potent aryl hydrocarbon receptor (AhR) antagonist with IC50 of 127 nM.
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BCC4663
Gadodiamide
Gadodiamide hydrate is a gadolinium-based contrast agent used in MR imaging procedures to assist in the visualization of blood vessels.
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BCC5563
URMC-099
URMC-099 is an orally bioavailable and potent mixed lineage kinase type 3 (MLK3) (IC50=14 nM) inhibitor with with excellent blood-brain barrier penetration properties.
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BCC7884
HA 130
HA130 is a selective autotaxin (ATX) inhibitor with an IC50 of 28 nM.
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BCC6105
PM 102
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BCC5861
740 Y-P
740 Y-P (PDGFR 740Y-P) is a potent and cell permeable PI3K activator.
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BCC6857
NS 398
NS-398 is a non-steroidal an-inflammatory agent with analgesic and antipyretic effects, and selectively inhibits prostaglandin G/H synthase 2/cyclooxygenase 2 (COX-2) activity, with an IC50 of 3.8 μM, and has no effect on COX-1 at 100 μM.
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BCC6034
Brain natriuretic peptide (1-32) (human)
Nesiritide (Brain Natriuretic Peptide-32 human) is an agonist of natriuretic peptide receptors (NPRs), with Kd values of 7.3 and 13 pM for NPR-A and NPR-C, respectively.
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BCC7110
CD 437
CD437 is a selective Retinoic Acid Receptor γ (RARγ) agonist.
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BCN2288
Vinorelbine Tartrate
Vinorelbine (ditartrate) is an anti-mitotic agent which inhibits the proliferation of Hela cells with IC50 of 1.25 nM.
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BCC8011
AbK
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BCC6191
SR 8278
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BCN2315
Pristimerin
Pristimerin is a potent and reversible monoacylglycerol lipase (MGL) inhibitor with an IC50 of 93 nM.
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BCN2346
Solasodine
Solasodine(Purapuridine) is a poisonous alkaloid chemical compound that occurs in plants of the Solanaceae family.
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BCC3832
Oxethazaine
Oxethazaine (Oxetacaine), a precursor of phentermine acidic, is an acid-resistent and orally active analgesic agent. Oxethazaine (Oxetacaine) has the potential for the relief of pain associated with peptic ulcer disease or esophagitis.
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BCC5456
BAPTA-AM
BAPTA-AM is a well-known membrane permeable Ca2+ chelator. BAPTA-AM inhibits hERG channels, hKv1.3 and hKv1.5 channels in HEK 293 cells with IC50s of 1.3 μM, 1.45 μM and 1.23 μM, respectively.
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BCC6219
NCX 466
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BCC7530
SR 12813
SR12813 is an inhibitor of 3-hydroxy-3-methylglutaryl-coenzyme A (HMG-CoA) reductase, with an IC50 value of 0.85 μM.
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BCC2050
VTP-27999 Hydrochloride
VTP-27999 Hcl is an alkyl amine Renin inhibitor; VTP-27999 is useful for Hypertension and End-Organ Diseases.
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BCC4068
Ulipristal acetate
Ulipristal acetate (CDB-2914) is an orally active, selective progesterone receptor modulator (SPRM). Ulipristal acetate stimulates the autophagic response selectively in leiomyoma cells. Ulipristal acetate has the potential for benign gynecological conditions treatment, such as uterine myoma.
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BCC5926
Locustatachykinin I
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BCC7587
Sodium acetate
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BCC1747
MI-3
MI-3 (Menin-MLL inhibitor 3) is a potent and high affinity menin-MLL inhibitor with an IC50 of 648 nM and a Kd of 201 nM.
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BCC1746
MI-2
Menin-MLL inhibitor MI-2 is a Menin-MLL interaction inhibitor with IC50 of 446±28 nM.
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BCC4015
(3S,4S)-3-(Boc-amino)-4-methylpyrrolidine
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BCC6033
C-type natriuretic peptide (1-22) (human, rat, swine)
C-Type Natriuretic Peptide (CNP) (1-22), human is the 1-22 fragment of C-Type Natriuretic Peptide. C-type natriuretic peptide is natriuretic peptide family peptide that is involved in the maintenance of electrolyte-fluid balance and vascular tone.
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BCC4945
Ursodiol
Ursodiol reduces cholesterol absorption and is used to dissolve gallstones.
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BCC6757
2-Hydroxypropyl-β-cyclodextrin
(2-Hydroxypropyl)-β-cyclodextrin is a widely used drug delivery vehicle to improve the stability and bioavailability.
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BCC1628
Hoechst 33258 analog 6
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BCC3719
Alendronate sodium
Inhibitor of farnesyl diphosphate synthase (FPPS) and osteoclast-mediated bone resorption
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BCC3690
Verteporfin
Verteporfin (CL 318952) is a photosensitizer for photodynamic therapy to eliminate the abnormal blood vessels in the eye associated with conditions such as age-related macular degeneration. Verteporfin is a YAP inhibitor which disrupts YAP-TEAD interactions. Verteporfin induces cell apoptosis.Verteporfinis an autophagy inhibitor that blocks autophagy at an early stage by inhibiting autophagosome formation.
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BCC8069
Tolfenpyrad
Tolfenpyrad is a pesticide that was first approved in 2002 in Japan.
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BCC5464
Amicarbazone
Amicarbazone(BAY-MKH3586; BAY314666) is a potent inhibitor of photosynthetic electron transport via binding to the Qb domain of photosystem II (PSII); herbicide with a broad spectrum of weed control.
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BCC3869
Thioridazine HCl
Selective inducer of CSC differentiation; anticancer agent,Thioridazine is an antipsychotic drug, used in the treatment of schizophrenia and psychosis, shows D4 selectivity or serotonin antagonism.
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BCC7544
AC 45594
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BCC6147
TC-F 2
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BCC7092
FR 122047 hydrochloride
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BCC4305
K145
K145 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 is inactive against SphK1 and other protein kinases. K145 induces cell apoptosis and has potently antitumor activity.
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BCC5445
Oxybenzone
Oxybenzone(Eusolex 4360; Escalol 567) is an organic compound used in sunscreens; provides broad-spectrum ultraviolet coverage, including UVB and short-wave UVA rays.
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BCC5468
Meptyldinocap
Meptyldinocap (2,4-DNOPC) is a novel powdery mildew (Erysiphe necator) fungicide which shows protectant and post-infective activities.
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BCC1786
NB-598
NB-598 is a potent and competitive inhibitor of squalene epoxidase (SE), and suppresses triglyceride biosynthesis through the farnesol pathway.
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BCC5883
PDZ1 Domain inhibitor peptide
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BCC7297
MNI caged kainic acid
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BCC3768
Diphenylpyraline HCl
Diphenylpyraline hydrochloride (4-Diphenylmethoxy-1-methylpiperidine hydrochloride) is a first-generation antihistamine with anticholinergic effects, acts as a dopamine reuptake inhibitor, shows to be useful in the treatment of Parkinsonism.
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BCC5333
(Z)-Pugnac
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BCC2067
YS-49
YS-49 is a PI3K/Akt (a downstream target of RhoA) activator, to reduce RhoA/PTEN activation in the 3-methylcholanthrene-treated cells. YS-49 inhibits angiotensin II (Ang II)-stimulated proliferation of VSMCs via induction of heme oxygenase (HO)-1. YS-49 is also an isoquinoline compound alkaloid, has a strong positive inotropic action through activation of cardiac β-adrenoceptors.
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BCC1633
HOE-S 785026
HOE-S 785026 is a blue fluorescent dyes, which can be used as a cell dye for DNA.
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BCC6491
3-Indolebutyric acid (IBA)
Indole-3-butyric acid (3-indolebutyric acid; IBA) is a plant growth auxin and a good rooting agent. It can promote herbs and woody ornamental plant rooting and used for improving fruit rate.
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BCC4872
Trichlormethiazide
Trichlormethiazide is a thiazide diuretic with properties similar to those of hydrochlorothiazide.
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BCC7987
Ethacrynic acid - d5
Ethacrynic acid D5 is a deuterium labeled Ethacrynic acid. Ethacrynic acid is a diuretic. Ethacrynic acid is an inhibitor of glutathione S-transferases (GSTs). Ethacrynic acid is a potent inhibitor of NF-kB-signaling pathway, and also modulates leukotriene formation. Ethacrynic acid also inhibits L-type voltage-dependent and store-operated calcium channel, leading to relaxation of airway smooth muscle (ASM) cells. Ethacrynic acid has anti-inflammatory properties that reduces the retinoid-induced ear edema in mice.
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BCC5616
3PO
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BCC8053
GSK2194069
GSK2194069 is a potent and specific inhibitor of the β-ketoacyl reductase (KR) activity of hFAS with an IC50 of 7.7 ± 4.1 nM in an assay detecting released CoA.
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BCC8064
PF 1022A
PF 1022A is a N-methylated cyclooctadepsipeptides (CODPs) with strong anthelmintic properties; acts as an ionophore.
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BCC6309
SR 1001
SR1001 is a selective RORα and RORγt inverse agonist with Kis 172 and 111 nM, respectively.
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BCC7972
LIMKi 3
BMS-5 (LIMKi 3) is a potent LIMK inhibitor with IC50s of 7 nM and 8 nM for LIMK1 and LIMK2, respectively.
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BCC5188
Methylcobalamin
Methylcobalamin (CH3-B12), a cobalamin, is a form of vitamin B12.
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BCC4034
Arginase inhibitor 1
Arginase inhibitor 1 is a potent inhibitor of human arginases I and II with IC50s of 223 and 509 nM, respectively.
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BCC6280
SA 57
SA57 is a potent, selective FAAH inhibitor with IC50s of 3.2 nM and 1.9 nM for mouse and human FAAH. SA57 also inhibits the 2-arachidonoylglycerol hydrolases MAGL (IC50s of 410 nM and 1.4 μM for mouse and human MAGL) and mouse α/β-hydrolase domain-containing protein 6 (mABHD6; IC50 of 850 nM), but not other brain serine hydrolases.
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BCC5462
kb-NB77-78
kb-NB77-78 is an analogue of CID797718, but shows no PKD inhibitory activity.
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BCC6142
JW 480
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BCC7463
CP 80633
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BCC6310
SR 2211
SR2211 is a potent, selective synthetic RORγ modulator and functions as an inverse agonist, with a Ki of 105 nM and an
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BCC4280
GNE-617
GNE-617 is a specific NAMPT inhibitor that inhibits the biochemical activity of NAMPT with an IC50 of 5 nM and exhibits efficacy in xenograft models of cancer.
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BCC6295
TAT 14
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BCC1753
MK-0591
Quiflapon (MK-591) is a selective and specific 5-lipoxygenase-activating protein (FLAP) inhibitor with an IC50 of 1.6 nM in a FLAP binding assay. Quiflapon is also a potent and orally active Leukotriene biosynthesis (LT) inhibitor, shows IC50 values of 3.1 and 6.1 nM in intact human and elicited rat PMNLs, respectively. Quiflapon induces cell apoptosis.
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BCC1787
NB-598 hydrochloride
NB-598 hydrochloride is a potent and competitive inhibitor of squalene epoxidase (SE), and suppresses triglyceride biosynthesis through the farnesol pathway.
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BCC1789
2-Mercaptoethanesulfonic acid
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BCC1891
Retinyl glucoside
Retinyl-β-D-glucoside is a naturally occurring and biologically active metabolites of vitamin A, which are found in fish and mammals.
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BCC6965
Nω-Propyl-L-arginine hydrochloride
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BCC5525
BRD4770
BRD4770 is a histone methyltransferase G9a inhibitor. BRD4770 reduces di- and trimethylation of lysine 9 on histone H3 (H3K9) with an EC50 of 5 µM, and has less or little effect toward H3K27me3, H3K36me3, H3K4me3, and H3K79me3. BRD4770 can activate the ataxia telangiectasia mutated (ATM) pathway and induce cell senescence.
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BCC6312
KML 29
KML29 is a potent and selective MAGL inhibitor with IC50 = 5.9, 15, and 43 nM in human, mouse, and rat brain proteomes, respectively.
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BCC1782
N3PT
N3PT(N3-pyridyl thiamine) is a potent and selective transketolase(TK) inhibitor (IC50= 22 nM for Apo-TK) both in vitro and in vivo.
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BCC7126
NKH 477
NKH477 (Colforsin dapropate hydrochloride) is a novel water-soluble forskolin derivative that improves cardiac failure mainly through its beneficial effects on diastolic cardiac function. NKH477 directly activates the catalytic unit of adenylate cyclase and increases intracellular cAMP. NKH477 exerts an antiproliferative effect in vivo with an altered cytokine profile to inhibit the acute rejection of rat orthotopic lung allografts.
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BCC5198
Vigabatrin Hydrochloride
Vigabatrin (Hydrochloride) (γ-Vinyl-GABA; Sabril) is a structural analog of the inhibitory neurotransmitter γ-aminobutyric acid (GABA) that irreversibly inhibits the catabolism of GABA by GABA transaminase.
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BCC6315
H2L5186303
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BCC6267
TC LPA5 4
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BCC6940
ATPA
ATPA is a selective glutamate receptor GluR5 activator with EC50s of 0.66, 9.5, 1.4, 23, 32, 18, and 14 μM for GluR5wt, GluR5(S741M), GluR5(S721T), GluR5(S721T, S741M), GluR5(S741A), GluR5(S741L), and GluR5(S741V), respectively.
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BCC6597
(S)-(-)-5-Iodowillardiine
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BCC1086
7-Methoxycoumarin-4-acetyl-P-L-G-L-β-(2,4-dinitrophenylamino)A-R amide
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BCC6317
ML 281
ML281 is a potent and selective STK33 inhibitor with IC50 of 14 nM.
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BCC6268
PF 06465469
PF-06465469 is a covalent inhibitor of ITK with an IC50 of 2 nM.
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BCC5442
5S rRNA modificator
5S rRNA modificator is a suitable electrophile for 2’-hydroxyl acylation on structured RNA molecules, yielding accurate structural information comparable to that obtained with existing probes; 5S rRNA RNA modification.
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BCC7005
LY 231617
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BCC1855
PF-543 Citrate
PF-543 Citrate (Sphingosine Kinase 1 Inhibitor II Citrate) is a potent, selective, reversible and sphingosine-competitive SPHK1 inhibitor with an IC50 of 2 nM and a Ki of 3.6 nM. PF-543 Citrate is >100-fold selectivity for SPHK1 over SPHK2. PF-543 Citrate is an effective potent inhibitor of sphingosine 1-phosphate (S1P) formation in whole blood with an IC50 of 26.7 nM. PF-543 Citrate induces apoptosis, necrosis, and autophagy.
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BCC6324
JW 642
JW 642 is a potent inhibitor of monoacylglycerol lipase (MAGL) that displays IC50 values of 7.6, 14, and 3.7 nM for inhibition of MAGL in mouse, rat, and human brain membranes, respectively.
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BCC7895
NPEC-caged-D-AP5
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BCC1315
9-Dihydro-13-acetylbaccatin III
9-Dihydro-13-acetylbaccatin III (9-DHAB III) is an intermediate for taxol analog preparations.
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BCC5667
L-690,488
L-690488 is a prodrug of L-690330 and is a selective inositol monophosphatase (IMPase) inhibitor. L-690488 has more effective cell penetration than L-690330.
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BCC5666
L-690,330
L-690330 is a competitive inhibitor of inositol monophosphatase (IMPase) with Kis of 0.27 and 0.19 μM for recombinant human and bovine IMPase, 0.30 and 0.42 μM for human and bovine frontal cortex IMPase, respectively. L-690330 exhibits 10-fold more sensitive than mouse and rat IMPase.
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BCC6203
A 484954
A-484954 is a highly selective eukaryotic elongationfactor-2 (eEF2) inhibitor, with an IC50 of 280 nM.
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BCC6586
Domoic acid
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BCC8061
ML216
ML216 (CID-49852229) is a potent, selective and cell permeable inhibitor of the DNA unwinding activity of BLM helicase with IC50s of 2.98 μM and 0.97 μM for BLMfull-length and BLM636-1298, respectively. ML216 inhibits ssDNA-dependent ATPase activity of BLM with a Ki of 1.76 µM. Antitumor avtivity.
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BCC6776
Tin protoporphyrin IX dichloride
Tin-protoporphyrin IX (SnPPIX) is a potent Heme oxygenase-1 (HO-1) inhibitor. Tin-protoporphyrin IX (SnPPIX) sensitizes pancreatic ductal adenocarcinoma (PDAC) tumors to chemotherapy in mice model.
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BCC5336
(Arg)9 peptide
(Arg)9 (Nona-L-arginine;Peptide R9) is a cell-penetrating peptide; exhibits neuroprotective activity with an IC50 of 0.78 μM in the glutamic acid model.
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BCC6362
L 012 sodium salt