Signaling Pathways(信号通路)
- Proteases(930)
- Apoptosis(596)
- Chromatin/Epigenetics(453)
- Metabolism(568)
- MAPK Signaling(99)
- Tyrosine Kinase(386)
- DNA Damage/DNA Repair(550)
- PI3K/Akt/mTOR Signaling(140)
- Microbiology & Virology(770)
- Cell Cycle/Checkpoint(256)
- Ubiquitination/ Proteasome(136)
- JAK/STAT Signaling(176)
- TGF-β / Smad Signaling(77)
- Angiogenesis(62)
- GPCR/G protein(568)
- Stem Cell(113)
- Membrane Transporter/Ion Channel(392)
- Cancer Biology(140)
- Endocrinology and Hormones(142)
- Neuroscience(643)
- Obesity, Appetite Control & Diabetes(81)
- Other Signal Transduction(24)
- Immunology/Inflammation(1110)
- Cardiovascular(145)
- Vitamin D Related(4)
- PROTAC(148)
- Ox Stress Reagents(82)
- Others(1312)
- Antiparasitics(18)
- Toxins(10)
- Cat.No. 产品名称 Information
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GC25289
CompK
compound K
CompK (compound K), a potent and selective hematopoietic progenitor kinase 1 (HPK1 or MAP4K1) small molecule inhibitor, significantly improves human T-cell functions, with enhanced T-cell receptor avidity to recognize tumor-associated antigens and tumor cytolytic activity by CD8+ T cells. -
GC25283
Colesevelam Hydrochloride
Colesevelam Hydrochloride is an orally administered, non-absorbable, polymeric, bile-acid-binding agent with a higher affinity for glycocholic acid in vitro
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GC25259
Cisapride hydrate
Propulsid, Alimix, Propulsin, Enteropride, Kinestase
Cisapride (Propulsid, Alimix, Propulsin, Enteropride, Kinestase) acts directly as a selective serotonin 5-HT4 receptor agonist with IC50 of 0.483 μM. And It also acts indirectly as a parasympathomimetic. -
GC25253
Cinitapride Hydrogen Tartrate
Cinitapride Hydrogen Tartrate is a gastroprokinetic agent that acts as an agonist of the 5-HT1 and 5-HT4 receptors and as an antagonist of the 5-HT2 receptors
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GC25249
CID-1517823
ML328
CID-1517823 (ML328) is a potent and selective inhibitor of bacterial AddAB and RecBCD helicase-nucleases, with IC50s of 1.0 and 4.8 μM. -
GC25239
chinifur
Chinifur, a selective inhibitor and "subversive substrate" for Trypanosoma congolense trypanothione reductase.
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GC25219
CH7233163
CH7233163 is a non-covalent ATP competitive inhibitor of EGFR-tyrosine kinase with antitumor activities against tumor with EGFR-Del19/T790M/C797S.
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GC25218
Cephradine monohydrate
Cefradine is a beta-lactam, first-generation cephalosporin antibiotic with bactericidal activity.
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GC25210
Ceftezole
Celoslin, Falomesin
Ceftezole (Celoslin, Falomesin) is a semi-synthetic first-generation cephalosporin with antibacterial activity. -
GC25209
Cefteram pivoxil
Cefteram Pivoxil is the pivalate ester prodrug of cefteram, a semi-synthetic, broad-spectrum, third-generation cephalosporin with antibacterial activity.
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GC25208
Cefatrizine
Cefatrizine, a broad-spectrum, semisynthetic, first-generation cephalosporin with antibacterial activity, binds to and inactivates penicillin-binding proteins (PBPs) located on the inner membrane of the bacterial cell wall.
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GC25197
Carvedilol EP IMpurity E
Carvedilol USP E, Carvedilol Impurity E
Carvedilol is a nonselective beta blocker/alpha-1 blocker and used in management of congestive heart failure (CHF). -
GC25188
Calcium 2-oxoglutarate
Calcium oxoglurate, Calcium 2-oxopentanedioate, Calcium α-ketoglutarate, Calcium AKG, Calcium 2-ketoglutaric acid, Calcium oxoglutaric acid
Calcium 2-oxoglutarate (Calcium oxoglurate, Calcium 2-oxopentanedioate, Calcium α-ketoglutarate, Calcium AKG, Calcium 2-ketoglutaric acid, Calcium oxoglutaric acid) is the Calcium salt form of 2-oxoglutarate. 2-oxoglutarate is naturally found in organisms and is a well-known intermediate in the production of ATP or GTP in the Krebs cycle. 2-oxoglutarate is a reversible inhibitor of tyrosinase with IC50 of 15 mM. -
GC25183
BZ1
BPTF inhibitor, BPTF-IN-BZ1
BZ1 (BPTF inhibitor, BPTF-IN-BZ1) is a pyridazinone-based BPTF (Bromodomain PHD Finger Transcription Factor) inhibitor with a high potency (Kd = 6.3 nM) and >350-fold selectivity over BET bromodomains. -
GC25182
Butoconazole
Butoconazole is an imidazole antifungal used in gynecology.
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GC25181
Butenafine
Butenafine is a synthetic benzylamine antifungal agent.
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GC25174
Brucine sulfate heptahydrate
Brucine is an alkaloid that acts as an antagonist at glycine receptors and paralyzes inhibitory neurons.
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GC25170
Bromhexine
Bromhexine is an expectorant/mucolytic agent used in the treatment of respiratory disorders associated with viscid or excessive mucus
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GC25168
Brepocitinib (PF-06700841)
PF-841
Brepocitinib (PF-06700841, PF-841) is a potent inhibitor of Tyk2 and Jak1 with IC50s of 23 nM, 17 nM, 77 nM for Tyk2, Jak1 and Jak2 respectively. It has appropriate in-family selectivity against JAK2 and JAK3. -
GC25164
Borofalan (10B)
SPM-011; Steboronine
Borofalan (10B) (SPM-011; Steboronine), a Ionising radiation emitter, can be used to treat the head and neck cancer. -
GC25160
BMS-1001
BMS-1001 is a potent inhibitor of PD-1/PD-L1 interaction with EC50 of 253 nM. BMS-1001 alleviates the inhibitory effect of the soluble PD-L1 on the T-cell receptor-mediated activation of T-lymphocytes.
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GC25159
BMF-219
BMF-219是一种高选择性和不可逆的menin抑制剂,在小鼠模型中具有良好的抑制效果 。
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GC25140
Bisoprolol
Bisoprolol is a cardioselective β1-adrenergic blocking agent used for secondary prevention of myocardial infarction (MI), heart failure, angina pectoris and mild to moderate hypertension.
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GC25139
Biphenyl-4-sulfonyl chloride
p-Phenylbenzenesulfonyl chloride, 4-Phenylbenzenesulfonyl chloride, p-Biphenylsulfonyl chloride
Biphenyl-4-sulfonyl chloride (p-Phenylbenzenesulfonyl, 4-Phenylbenzenesulfonyl, p-Biphenylsulfonyl) is a HDAC inhibitor with synthetic applications in palladium-catalyzed desulfitative C-arylation. -
GC25137
Betrixaban maleate
Betrixaban maleate is the maleate salt form of Betrixaban, which is a Factor Xa inhibitor that decreases prothrombinase activity and thrombin generation.
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GC25136
Betazole Dihydrochloride
Ametazole Dihydrochloride, 2-(3-Pyrazolyl)ethanamine Dihydrochloride
Betazole Dihydrochloride (Ametazole, 2-(3-Pyrazolyl)ethanamine) is a histamine H2 agonist used clinically to test gastric secretory function. -
GC25135
Besifloxacin
Besifloxacin is a fourth generation fluoroquinolone-type opthalmic antibiotic for the treatment of bacterial conjunctivitis.
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GC25134
Benzocaine hydrochloride
Ethyl 4-aminobenzoate hydrochloride, Benzocaine HCl, Ethyl p-aminobenzoate hydrochloride
Benzocaine hydrochloride (Ethyl 4-aminobenzoate, Ethyl p-aminobenzoate) is a surface anesthetic that acts by preventing transmission of impulses along nerve fibers and at nerve endings. -
GC25120
Balixafortide (POL6326)
Balixafortide (POL6326) is an orally bioavailable peptidic CXC chemokine receptor 4 (CXCR4) antagonist
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GC25117
Azvudine
RO-0622
Azvudine (RO-0622) is a novel nucleoside reverse transcriptase inhibitor with antiviral activity against human immunodeficiency virus (HIV), hepatitis B virus (HBV) and hepatitis C virus (HCV), potently inhibits HIV-1 (EC50 range 0.03 to 6.92 nM) and HIV-2 (EC50s ranging from 0.018 to 0.025 nM). -
GC25097
AQX-016A
AQX-016A is a potent agonist of SHIP1. AQX-016A inhibits DNFB induced inflammation in a mouse ear edema/cutaneous anaphylaxis model.
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GC25075
Ansamitocin p-3 (Maytansinol isobutyrate, NSC292222)
Antibiotic C 15003P3
Ansamitocin p-3 (Maytansinol isobutyrate, NSC292222, Antibiotic C 15003P3) is a potent inhibitor of tubulin polymerization with IC50 of 3.4 μM. -
GC25060
Amitriptyline
MK-230, N-750, Ro41575
Amitriptyline (MK-230, N-750, Ro41575) is a tricyclic antidepressant (TCA) with analgesic properties, widely used to treat depression and neuropathic pain. Amitriptyline is an inhibitor of both serotonin transporter (SERT) and norepinephrine transporter (NET) with Ki of 3.45 nM and 13.3 nM, respectively. Amitriptyline also inhibits histamine receptor H1, histamine receptor H4, 5-HT2 and sigma 1 receptor with Ki of 0.5 nM, 7.31 nM, 235 nM and 287 nM, respectively. This product is a waxy solid. -
GC25059
Alverine
Alverine is a smooth muscle relaxant.
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GC25058
Aluminum potassium sulfate
APS
Aluminum potassium sulfate (APS) and tannic acid (ALTA) sclerotherapy are often used to treat hemorrhoids. Aluminum potassium sulfate induces learning and memory deficits in mice. -
GC25051
Alloxazine
Isoalloxazine
Alloxazine (Isoalloxazine) is an A2 receptor antagonist, which is approximately 10-fold more selective for the A2B receptor than for the A2A receptor. -
GC25046
Albiglutide Fragment
Albiglutide fragment is one copy of a 30-amino-acid sequence of modified human GLP-1 (fragment 7-36).
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GC25039
AG-120 (racemic)
AG-120 (racemic), the racemic mixture of AG-120, is an orally available inhibitor of isocitrate dehydrogenase type 1 (IDH1) with potential antineoplastic activity.
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GC25037
Adenosine 5′-diphosphate sodium salt
Adenosine diphosphate sodium salt, ADP sodium salt, Adenosine 5′-pyrophosphate sodium salt, Adenosine pyrophosphate sodium salt
Adenosine 5′-diphosphate (ADP, Adenosine diphosphate, Adenosine 5′-pyrophosphate, Adenosine pyrophosphate) is an important organic compound in metabolism and is essential to the flow of energy in living cells. ADP can be interconverted to adenosine triphosphate (ATP) and adenosine monophosphate (AMP). -
GC25035
Acrylamide monomer
Acrylamide is a neurotoxic monomer with extensive industrial applications. It could be used as a precursor to polyacrylamides.
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GC25027
Absinthin
Absynthine
Absinthin (Absynthine) is a naturally produced triterpene lactone from Artemisia absinthium with anti-inflammatory properties. Absinthin significantly enhances the expression of matrix metalloproteinase-8 (MMP-8) and is a possible treatment candidate for Acute lung injury (ALI). -
GC25025
Abraxane
Nab-Paclitaxel
Abraxane (Nab-Paclitaxel), a novel solvent-free taxane with the binding ratio of Paclitaxel to human serum albumin of 1:9, is an anti-microtubule drug that promotes microtubule aggregation in tubulin dimer and inhibits microtubule depolymerization to stabilize the microtubule system. -
GC25024
7-Hydroxycarbostyril
3,4-Dihydro-7-hydroxycarbostyril
7-Hydroxycarbostyril (3,4-Dihydro-7-hydroxycarbostyril) is a kind of pharmaceutical intermediate. -
GC25023
7,8-Dimethoxy-4H-chromen-4-one
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GC25022
6-Chloro-7-hydroxy-4-methylcoumarin
6-Chloro-7-hydroxy-4-methylcoumarin is a pharmaceutical intermediate.
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GC25020
5-Bromocytosine
5-Bromocytosine can be used in the synthesis of cross-link products under anaerobic and aerobic conditions.
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GC25019
5-amino-2,4-dimethylpyridine (5A-DMP)
5-amino-2,4-dimethylpyridine (5A-DMP) is a novel tandem Tudor domain (TTD)-binding compound that inhibits the full-length UHRF1:LIG1 interaction in Xenopus egg extracts
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GC25018
4-Vinylcyclohexene dioxide
Vinylcyclohexene dioxide, VCD
4-Vinylcyclohexene dioxide(VCD)是4-乙烯基环己烯(VCH)的代谢产物,在工业上被合成为环氧树脂和其他环氧化物的中间稀释剂。 -
GC25017
4,4'-Bis(4-aminophenoxy)biphenyl
4,4'-Bis(4-aminophenoxy)biphenyl is a monomer for polyimide production.
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GC25016
3-Amino-9-ethylcarbazole
AEC
3-Amino-9-ethylcarbazole (AEC) is a chemical compound commonly used as a chromogenic substrate in immunohistochemistry, specifically for visualizing sections stained with HRP-conjugated secondary antibodies.