Signaling Pathways(信号通路)
- Proteases(1069)
- Apoptosis(506)
- Chromatin/Epigenetics(349)
- Metabolism(806)
- MAPK Signaling(89)
- Tyrosine Kinase(353)
- DNA Damage/DNA Repair(469)
- PI3K/Akt/mTOR Signaling(126)
- Microbiology & Virology(940)
- Cell Cycle/Checkpoint(282)
- Ubiquitination/ Proteasome(117)
- JAK/STAT Signaling(124)
- TGF-β / Smad Signaling(58)
- Angiogenesis(64)
- GPCR/G protein(568)
- Stem Cell(97)
- Membrane Transporter/Ion Channel(477)
- Cancer Biology(237)
- Endocrinology and Hormones(190)
- Neuroscience(837)
- Obesity, Appetite Control & Diabetes(97)
- Other Signal Transduction(43)
- Immunology/Inflammation(1199)
- Cardiovascular(288)
- Vitamin D Related(6)
- PROTAC(85)
- Ox Stress Reagents(125)
- Others(1265)
- Antiparasitics(26)
- Toxins(20)
- Cat.No. 产品名称 Information
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GC26063
WAY-340935
VEGFR2-IN-2
WAY-340935 (VEGFR2-IN-2) can inhibit the function of VEGFR2 and the anti-proliferative activity against the H460 cell line is produced partly by interaction of VEGFR protein. - GC26062 WAY-328178 WAY-328178 is a bioactive compound.
- GC26061 WAY-328168 WAY-328168 is a bioactive compound.
- GC26060 WAY-328133 WAY-328133 is a bioactive compound.
- GC26059 WAY-323096
- GC26057 WAY-309236-A
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GC26056
WAY-303290
GluR6 antagonist-1
WAY-303290 (GluR6 antagonist-1) is a benzothiophene derivative acting as an ionotropic glutamate receptor 6 (GluR6) antagonist, which can be used for researching acute and chronic neurological disorders. -
GC26055
WAY-301398
6-methoxynaphthalene
WAY-301398 (6-methoxynaphthalene) can bind to protein kinase C (PKC). - GC26054 WAY-299775 WAY- 299775 is a bioactive compound.
- GC26053 WAY-297848 WAY-297848 is a novel glucokinase activator with potential use as a drug for the prevention or treatment of hyperglycemia, diabetes, obesity, dyslipidemia, metabolic syndrome, etc.
- GC26052 WAY-297407 WAY-297407 is a bioactive compound.
- GC26051 WAY-296817
- GC26050 WAY-272077
- GC26049 WAY-119064 WAY-119064 is a potent glycogen synthase kinase-3β (GSK-3β) inhibitor with an IC50 value of 80.5 nM.
- GC26046 Waltonitone Waltonitone, an ursane-type pentacyclic triterpene extracted from Gentiana waltonii Burkill, exerts anti-tumor effect.
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GC26044
VPS34 inhibitor 1 (Compound 19)
PIK-III analogue
VPS34 inhibitor 1 (Compound 19, PIK-III analogue) is a potent and selective inhibitor of VPS34 with an IC50 of 15 nM. -
GC26035
Verubecestat (MK-8931) Trifluoroacetate
MK-8931
Verubecestat (MK-8931) Trifluoroacetate is a potent and selective beta-secretase inhibitor and BACE1 protein inhibitor or Beta-site APP-cleaving enzyme 1 inhibitor. -
GC26033
Veratrine
Cevadine, Cevadin, Cevadene
Veratridine (Cevadine, Cevadin, Cevadene), a steroidal alkaloid found in plants of the lily family, is a voltage-gated sodium channel activator. Veratridine induces anxiogenic-like behaviors in rats. -
GC26032
Varenicline (CP 526555) dihydrochloride
Chantix, Champix,CP 526555 dihydrochloride
Varenicline (CP 526555, Chantix, Champix,CP 526555 dihydrochloride) dihydrochloride is a potent, partial agonist of α4β2 nicotinic acetylcholine receptor (nAChR) and α3β4 nAChR with EC50 of 2.3 μM and 55 μM, respectively. Varenicline dihydrochloride is a potent, full agonist of α7 nAChRs with EC50 of 18 μM. Varenicline is a prescription medication used for smoking cessation. -
GC26029
Valbenazine tosylate
NBI-98854
Valbenazine tosylate (NBI-98854) is the tosylate salt of valbenazine, a vesicular monoamine transporter 2 (VMAT2) inhibitor with a Ki value of 150 nM while displaying no significant binding to VAMT1(Ki<10 μM). - GC26027 V-0219 V-0219 is an orally active, positive allosteric modulator (PAM) of the glucagon-like peptide-1 receptor (GLP-1R), can be used for obesity-associated diabetes research.
- GC26017 UK-371804 HCl UK-371804 is a potent and selective urokinase-type plasmogen activator (uPA) inhibitor with excellent enzyme potency (Ki=10 nM) and selectivity profile (4000-fold versus tPA and 2700-fold versus plasmin).
- GC26016 TSHR antagonist S37 TSHR antagonist S37 is a selective and competitive antagonist of the thyrotropin receptor (TSHR).
- GC26012 Tris(2-ethylhexyl) phosphate Tris (2-ethylhexyl) phosphate, a clear, viscous liquid, is used as a component of vinyl stabilizers, grease additives, and flame-proofing compositions; however, it is used primarily as a plasticizer for vinyl plastic and synthetic rubber compounds.
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GC26011
Tris(2-butoxyethyl) phosphate
TBEP
Oral exposure to low-dose Tris (2-butoxyethyl) phosphate (TBEP) levels equivalent to tolerable daily intake may exacerbate allergic pulmonary inflammation by promoting a skewed T-helper 2 cell response, upregulation of ERα and dysregulation of both MLN and BM microenvironments. - GC26007 Tridecafluorohexane-1-sulfonic acid potassium salt Tridecafluorohexane-1-sulfonic acid potassium salt is a perfluoroanionic surfactant, which is mainly used as a chromium mist inhibitor in electroplating, a wetting agent, and an additive in fluoroprotein foam fire extinguishing agents.DMSO is not recommended to dissolve platinum-based drugs, which can easily lead to drug inactivation.
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GC26002
Trazodone
AF-1161
Trazodone (AF-1161) is a 5-HT 2A/2C receptor antagonist that is used as an antidepressant for treating major depressive disorder and anxiety disorders. - GC26001 TPX-0046 TPX-0046 is a novel RET/SRC inhibitor with a mean IC50 of 17 nM for RETG810R in Ba/F3 cell proliferation assay
- GC26000 TP0427736 HCl TP0427736 is a potent inhibitor of ALK5 kinase activity with an IC50 of 2.72 nM and this effect is 300-fold higher than the inhibitory effect on ALK3 (IC50 = 836 nM for ALK3). It also inhibits Smad2/3 phosphorylation in A549 cells induced by TGF-β1 with an IC50 value of 8.68 nM.
- GC25996 THZ1 2HCl THZ1 is a covalent CDK7 inhibitor which has the unprecedented ability to target a remote cysteine residue located outside of the canonical kinase domain, providing an unanticipated means of achieving selectivity for CDK7.
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GC25994
Thonzylamine
Neohetramine
Thonzylamine (Neohetramine) is an antihistamine and anticholinergic drug. - GC25993 TH263 TH-263, a diaryl sulfonamide derivative, is inactive toward both LIMK1 and LIMK2 and thus can be used as negative control for TH-257.
- GC25992 TG-89 TG-89 is an inhibitor of JAK2 with IC50 of 11.2 μM.
- GC25991 tetrathiomolybdate Tetrathiomolybdate (TM) is used in the clinic for the treatment of Wilson's disease by inducing dimerization of the metal-binding domain of the cellular copper efflux protein ATP7B (WLN4) through a unique sulfur-bridged Mo2S6O2 cluster.
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GC25986
TCPP
Tris (clorisopropyl)phosphate
TCPP (Tris(2-chloroethyl) phosphate) is a pervasive flame retardant. -
GC25985
TC-067533
2-Methyl-N-(1S-naphthalen-2-yl-ethyl)-benzamide
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GC25982
Tanzisertib(CC-930)
JNK-930, JNKI-1
Tanzisertib (CC-930, JNK-930, JNKI-1) is kinetically competitive with ATP in the JNK-dependent phosphorylation of the protein substrate c-Jun and potent against all isoforms of JNK (Ki(JNK1) = 44 ± 3 nM, IC50(JNK1) = 61 nM, Ki(JNK2) = 6.2 ± 0.6 nM, IC50(JNK2) = 5 nM, IC50(JNK3) = 5 nM) and selective against MAP kinases ERK1 and p38a with IC50 of 0.48 and 3.4 μM respectively. -
GC25973
Sulfamide
Sulfuric diamide
Sulfamide (Sulfuric diamide) is used in organic chemistry for synthesis. - GC25972 Sulfamethoxazole sodium Sulfamethoxazole sodium is an antibiotic used for bacterial infections.
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GC25969
SU5208
3-[(Thien-2-yl)methylene]-2-indolinone
SU5208(3-[(Thien-2-yl)methylene]-2-indolinone) is an inhibitor of vascular endothelial growth factor receptor-2 (VEGFR2). - GC25968 STK414603
- GC25963 SR-0813 SR-0813 is a potent and selective ENL/AF9 YEATS domain inhibitor. SR-0813 has IC50 values of 25 and 311 nM for ENL YEATS domain and AF9 YEATS domain, respectively.
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GC25942
Sodium Glucoheptonate Dihydrate
Sodium glucoheptonate
Sodium glucoheptonate is used for cleaning metal, mercerizing, paint stripping, and aluminum etching. - GC25941 Sodium acrylate Sodium acrylate is a metal salt that can be prepared by an acid-base reaction between sodium hydroxide and acrylic acid.
- GC25940 SNS-314 SNS-314 is a potent and selective inhibitor of Aurora A, Aurora B and Aurora C with IC50 of 9 nM, 31 nM, and 3 nM, respectively. It is less potent to Trk A/B, Flt4, Fms, Axl, c-Raf and DDR2. Phase 1.
- GC25936 SLC13A5-IN-1 SLC13A5-IN-1 is a selective inhibitor of sodium-citrate co-transporter (SLC13A5/NaCT). It completely blocks the uptake of 14 C-citrate and has the potential for the treatment of metabolic and/or cardiovascular diseases.
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GC25935
Simufilam dihydrochloride
PTI-125 dihydrochloride
Simufilam (PTI-125) Dihydrochloride is a small molecule modulator that preferentially binds altered FLNA and restores its native conformation, restoring receptor and synaptic activities and reducing its α7nAChR/TLR4 associations and downstream pathologies. - GC25913 Selective PI3Kδ Inhibitor 1 (compound 7n) Selective PI3Kδ Inhibitor 1 (compound 7n) is an inhibitor of PI3Kδ with an IC50 of 0.9 nM and >1000-fold selectivity against other class I PI3K isoforms [PI3K α/γ/β=3670/1460/21300 nM].
- GC25900 Scarlet 808 Scarlet 808 is a chemical dye.
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GC25899
SC-1
1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea, STAT3-IN-7
SC-1 (1-(4-Chloro-3-(trifluoromethyl)phenyl)-3-(4-(4-cyanophenoxy)phenyl)urea, STAT3-IN-7), a Sorafenib analogue and potently inhibits the phosphorylation of STAT3, induces cell apoptosis through SHP-1 dependent STAT3 inactivation.