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
-
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.
-
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
Potassium perfluorohexanesulfonate
Tridecafluorohexane-1-sulfonic acid potassium salt是一种全氟阴离子表面活性剂,主要用作电镀中的铬雾抑制剂、润湿剂、氟蛋白泡沫灭火剂中的添加剂。 -
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.
-
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.
-
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
-
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.
-
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.
-
GC25942
Sodium Glucoheptonate Dihydrate
Sodium glucoheptonate
Sodium glucoheptonate is used for cleaning metal, mercerizing, paint stripping, and aluminum etching. -
GC25941
Sodium acrylate
Sodium acrylate是一种金属盐,可通过氢氧化钠和丙烯酸的酸碱反应制备。
-
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.
-
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.
-
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. -
GC25898
SB 200646
SB 200646A
SB 200646 (SB 200646A) is a potent, selective and oral-active antagonist of 5-HT2B/2C over 5-HT2A receptor with 50 fold selectivity. The pKi for rat 5-HT2C receptor, rat 5-HT2B receptor and rat 5-HT2A receptor are 6.9, 7.5 and 5.2, respectively. SB 200646 has electrophysiological and anxiolytic properties in vivo. -
GC25889
Santalol
Santalol is a naturally occuring sesquiterpene that has antibacterial, anti-hyperglycaemic, anti inflammatory and antioxidant effects.
-
GC25881
S961
S961 is a biosynthetic insulin receptor antagonist that inhibits cellular proliferation and colony formation in breast tumour cells.
-
GC25869
RO495
CS-2667
RO495 (CS-2667) is a potent inhibitor of Non-receptor tyrosine-protein kinase 2 (TYK2). -
GC25867
Rilpivirine Hydrochloride
TMC278
Rilpivirine (TMC278), is a second-generation non-nucleoside reverse transcriptase inhibitor (NNRTI) with higher potency, longer half-life and reduced side-effect profile compared with older NNRTIs, such as efavirenz. -
GC25863
Riamilovir
Triazavirin
Riamilovir (Triazavirin) is a broad-spectrum antiviral drug candidate, which can be used for potential application against the Coronavirus 2019-nCoV. -
GC25848
RH01687
RH01687 is a potent β-cell protector that exhibits β-cell-protective activities against endoplasmic reticulum (ER) stress.
-
GC25832
Raloxifene
Keoxifene, Pharoxifene, LY-139481, LY-156758, CCRIS-7129
Raloxifene (Keoxifene, Pharoxifene, LY-139481, LY-156758, CCRIS-7129) is a second generation selective estrogen receptor modulator (SERM) used to prevent osteoporosis in postmenopausal women. -
GC25812
Quinidine sulfate
Chinidin Sodium, Pitayine Sodium, β-quinine Sodium, (+)-quinidine Sodium
Quinidine (Chinidin, Pitayine, β-quinine, (+)-quinidine) acts as a blocker of voltage-gated sodium channels, also an antimuscarinic and antimalarial.
-
GC25787
PRT-060318 2HCl
PRT318
PRT-060318 (PRT318) is a novel selective inhibitor of the Syk tyrosine kinase with an IC50 of 4 nM, as an approach to HIT treatment. -
GC25786
Propafenone
SA-79
Propafenone (SA-79) is an orally active sodium channel blocking agent and a beta-adrenoceptor (β-adrenergic receptor) antagonist. Propafenone offers a broad spectrum of activity in the treatment of cardiac arrhythmias. -
GC25785
Promethazine
Promethazine is a potent histamine H1 receptor antagonist. Promethazine is a medication used in the management and treatment of allergic conditions, nausea and vomiting, motion sickness, and sedation. Promethazine exhibits antiparasitic properties.
-
GC25784
Proflavine
3,6-Diaminoacridine
Proflavine (3,6-Diaminoacridine) is a disinfectant bacteriostatic against many gram-positive bacteria. It is a topical antiseptic used mainly in wound dressings. -
GC25782
Procaine penicillin G
PGP, Penicillin G Procaine, Bicillin C-R
Penicillin G Procaine (PGP, Penicillin G Procaine, Bicillin C-R), a crystalline complex combining penicillin G with procaine, is a β-lactam antibiotic. -
GC25780
Potassium thioacetate
Potassium thioacetate is widely used as a sulfur source in the synthesis of sulfur-containing organic compounds. It has been employed for the synthesis of heterocycles, polymers, transition-metal ligands, nanoparticles, bioactive compounds and macromolecular inclusion complexes.
-
GC25779
Potassium phosphate dibasic
Dipotassium phosphate
Potassium phosphate dibasic (Dipotassium phosphate, K2HPO4) is often used as a fertilizer, food additive, and buffering agent.