其他產(chǎn)品及廠家

2-HYDROXY-3,4-DIMETHOXYBENZOIC ACID；2-羥基-3,4-二甲氧基苯甲酸2-HYDROXY-3,4-DIMETHOXYBENZOIC ACID
2-hydroxy-3,4-dimethoxybenzoic acid is a natural product.
更新時間:2025-09-05
Gymconopin C；化合物 Gymconopin CGymconopin C
gymconopin c exhibits antiallergic properties, effectively reducing passive cutaneous anaphylaxis reactions in mouse ears.
更新時間:2025-09-05
GW274150 dihydrochloride；化合物 GW274150 dihydrochlorideGW274150 dihydrochloride
gw274150 (dihydrochloride) is a potent, selective inhibitor of human and rat inducible nitric oxide synthase (inos), exhibiting oral activity and nadph-dependence with an ic50 of 2.19 μm and kd of 40 nm for human inos, and an ed50 of 1.15 μm for rat inos. it demonstrates reduced effectiveness against endothelial nos (enos) and neuronal nos (nnos) in both species. the compound has been shown to confer protective effects in acute lung injury inflammation models [1] [2] [3].
更新時間:2025-09-05
GTPγS tetralithium；化合物 GTPγS tetralithiumGTPγS tetralithium
gtpγs (tetralithium) is a g-protein activator known for its role in preventing proteolytic degradation of proteins, facilitating tyrosine kinase-dependent glut4 translocation, stimulating phospholipases, and promoting actin polymerization. it is utilized to couple with g-protein α for the investigation of kinase activity effects and serves as a component of lysis buffer [1] [2] [3] [4].
更新時間:2025-09-05
GSPT1 degrader-2；化合物 GSPT1 degrader-2GSPT1 degrader-2
gspt1 degrader-2 is a potent degrader of gspt1 [1].
更新時間:2025-09-05
GSK-LSD1；化合物 GSK-LSD1GSK-LSD1
gsk-lsd1, an lsd1 inhibitor, decreases food consumption and body weight while enhancing insulin sensitivity and glycemic regulation in murine obesity models. additionally, it mitigates non-alcoholic fatty liver disease (nafld) and suppresses cytokine release induced by sars-cov-2 in covid-19 peripheral blood mononuclear cells (pbmcs). furthermore, gsk-lsd1 inhibits the proliferation and spread of cancer [1] [2] [3].
更新時間:2025-09-05
GsAF-1；化合物 GsAF-1GsAF-1
gsaf-1, a peptide toxin with three disulfide bonds, is derived from the venom of the chilean pink tarantula and has potential applications in the research of moderate-to-severe pain [1].
更新時間:2025-09-05
Grosshemin；化合物 GrossheminGrosshemine；Grosshemine
grosshemin, also known as grosshemine, is a natural compound identified in the siberian population of centaurea scabiosa [1].
更新時間:2025-09-05
GRL-1720 TFA；化合物 GRL-1720 TFAGRL-1720 TFA
grl-1720 tfa is a potent sars-cov-2 mpro inhibitor, demonstrating anti-sars-cov-2 activity with an ec50 of 15 μm [1].
更新時間:2025-09-05
GRL018-21；化合物 GRL018-21GRL018-21
grl018-21 is a potent, highly selective inhibitor of g protein-coupled receptor kinase 5 (grk5), exhibiting an ic50 of 10 nm [1].
更新時間:2025-09-05
Grisnilimab setaritox；化合物 Grisnilimab setaritoxWT1-RTA；WT1-RTA
grisnilimab setaritox (wt1-rta), an anti-cd7 antihuman t cell antibody linked to ricin a chain (rta), exhibits in vitro cytotoxicity against cem (t-lymphoblastic leukemia) cells with an id 50 of 53 pm. the 30-kda rta component disrupts the function of 60s ribosomal subunits. additionally, grisnilimab setaritox has demonstrated efficacy in ameliorating leukemic meningitis in a rhesus monkey model [1].
更新時間:2025-09-05
Cue-lure；誘蠅酮Q-lure|||Pherocon (4-(4-Acetoxyphenyl)-2-butanone)；Q-lure|||乙酸覆盆子酮酯|||誘蠅酮|||Pherocon (4-
cue-lure (pherocon (4-(4-acetoxyphenyl)-2-butanone)) is a standard melon fly attractant
更新時間:2025-09-05
Grisnilimab；化合物 GrisnilimabWT1；WT1
"grisnilimab (wt1), an igg2a monoclonal antibody targeting cd7, acts as a tumor suppressor in the pathogenesis of wilms´ tumor. it modulates the transcription of various genes and may be involved in post-transcriptional rna processing [1]."
更新時間:2025-09-05
Grb2 SH2 domain inhibitor 1；化合物 Grb2 SH2 domain inhibitor 1Grb2 SH2 domain inhibitor 1
grb2 sh2 domain inhibitor 1 is a cyclic cell-penetrating peptide (cpp) featuring a conformationally restricted d-pro-l-pro motif ring (af φ rpprrfq), where φ represents l-naphthylalanine, r denotes d-arginine, and p indicates d-proline. this compound primarily functions as a cyclic peptide inhibitor.
更新時間:2025-09-05
Grandivine A；化合物 Grandivine AGrandivine A
grandivine a, a steroid alkaloid, has been isolated from veratrum grandiflorum [1].
更新時間:2025-09-05
GPR61 Inverse agonist 1；化合物 GPR61 Inverse agonist 1GPR61 Inverse agonist 1
compound 1, identified as a gpr61 inverse agonist, exhibits an ic50 of 11 nm, rendering it suitable for metabolism and body weight disorder research, including obesity and cachexia [1].
更新時間:2025-09-05
GPR34 receptor antagonist 3；化合物 GPR34 receptor antagonist 3GPR34 receptor antagonist 3
compound 5e, a gpr34 receptor antagonist, exhibits selective inhibition of lysophosphatidylserine-induced erk1/2 phosphorylation in a dose-dependent manner, demonstrating an ic50 value of 0.680 μm without significant cytotoxicity. additionally, it displays antisensory activity in a mouse neuropathic pain model [1].
更新時間:2025-09-05
GPR3 agonist-2；化合物 GPR3 agonist-2GPR3 agonist-2
gpr3 agonist-2 (compound 32) is a potent full agonist of the g protein-coupled receptor 3 (gpr3), exhibiting an ic50 value of 260 nm [1].
更新時間:2025-09-05
GPR139 agonist-2；化合物 GPR139 agonist-2GPR139 agonist-2
gpr139 agonist-2 (compound 20a), a potent gpr139 agonist with an ec50 of 24.7 nm, has demonstrated efficacy in rescuing social interaction deficits and alleviating cognitive deficits in murine schizophrenia models, indicating its potential in antischizophrenia drug research [1].
更新時間:2025-09-05
GPAT-IN-1；化合物 GPAT-IN-1GPAT-IN-1
gpat-in-1, a glycerol-3-phosphate acyltransferase (gpat) inhibitor, exhibits an inhibitory concentration (ic50) of 8.9 μm and is utilized in obesity research [1].
更新時間:2025-09-05
Gotistobart；化合物 GotistobartBNT 316|||ONC-392；BNT 316|||ONC-392
gotistobart (onc-392) is a humanized anti-ctla-4 antibody that enhances immunotherapy by selectively depleting regulatory t cells (treg) within the tumor microenvironment [1].
更新時間:2025-09-05
Gossypetin 3-sophoroside-8-glucoside；化合物 Gossypetin 3-sophoroside-8-glucosideGossypetin 3-sophorosid
gossypetin 3-sophoroside-8-glucoside, a flavonol glycoside, is extractable from the aerial parts of equisetum hyemale l. [1].
更新時間:2025-09-05
Goshuyuamide I；化合物 Goshuyuamide IGoshuyuamide I
goshuyuamide-i (compound 4), an alkaloid, can be isolated from the fruits of euodia rutaecarpa and is utilized in analgesic research [1].
更新時間:2025-09-05
Golocdacimab；化合物 GolocdacimabMEDI6570；MEDI6570
golocdacimab (medi6570) is a fully human monoclonal antibody targeting lox-1 with potential application in type 2 diabetes research [1].
更新時間:2025-09-05
Gol-NTR；化合物 Gol-NTRGol-NTR
gol-ntr, a highly selective and sensitive golgi-targetable probe, is activated by nitroreductase (ntr) to visualize acute lung injury (ali) and its repair. with a low detection limit of 54.8 ng/ml, gol-ntr is well-suited for research focused on monitoring and assessing the response of sepsis-induced ali [1].
更新時間:2025-09-05
Gochnatiolide A；化合物 Gochnatiolide AGochnatiolide A
gochnatiolide a, a dimeric sesquiterpene isolated from ainsliaea henryi, demonstrates antiproliferative properties against various cell lines, including kidney, melanoma, ovarian-resistant, and glioma [1] [2].
更新時間:2025-09-05
Gnetuhainin I；化合物 Gnetuhainin IGnetuhainin I
gnetuhainin i (compound 5), a lignin sourced from pouzolzia zeylanica, exhibits potent inhibition of atp citrate lyase (acly) with an ic50 value of 2.63 μm [1].
更新時間:2025-09-05
GNE-235；化合物 GNE-235GNE-235
gne-235, a selective inhibitor of pbrm1´s second bromodomain, exhibits a dissociation constant (k d) of 0.28 ± 0.02 μm, and can be utilized to assess the cellular function of pbrm1 [1].
更新時間:2025-09-05
GMPRGA；化合物 GMPRGAGMPRGA
gmprga, a derivative of spbeta phages, identifies spaimr within the bacterial cytosol to trigger lysogeny [1].
更新時間:2025-09-05
GM1a Ganglioside oligosaccharide；化合物 GM1a Ganglioside oligosaccharideGM1a Ganglioside oligosaccharid
gm1a ganglioside oligosaccharide, a semisynthetic derivative of ganglioside gm1, serves as the natural receptor for cholera toxin and is crucial for both general growth regulation and the coupling of hormone-induced responses [1].
更新時間:2025-09-05
Glyurallin B；化合物 Glyurallin BGlyurallin B
glyurallin b, a flavonoid derived from glycyrrhiza inflata and glycyrrhiza uralensis (licorice), exhibits abts+ radical scavenging activity and lipid peroxidation inhibition, with ec50 values of 11.9 ± 0.58 μm and 15.3 ± 1.26 μm, respectively [1].
更新時間:2025-09-05
Gly-Mal-Gly-Gly-Phe-Gly-amide-methylcyclopropane-Exatecan；化合物 Gly-Mal-Gly-Gly-Phe-Gly-amide-methylcy
gly-mal-gly-gly-phe-gly-amide-methylcyclopropane-exatecan is a compound utilized in the synthesis of antibody-drug conjugates (adcs) [1].
更新時間:2025-09-05
Ethyl chrysanthemate；菊酸乙酯Ethyl chrysanthemumate；菊酸乙酯|||Ethyl chrysanthemumate
ethyl chrysanthemate (ethyl chrysanthemumate) is an allelochemical compound used as an attractant
更新時間:2025-09-05
Gly-Gly-Arg；化合物 Gly-Gly-ArgGly-Gly-Arg
gly-gly-arg, a tripeptide and "pumping pheromone," is released from hatching eggs, stimulating pleopod pumping activity in subtidal crustaceans at a threshold concentration of 10 nm and eliciting a maximum response rate of 58.3%. additionally, this compound plays a role in controlling larval release in these organisms [1].
更新時間:2025-09-05
Gly-Gly-AMC；化合物 Gly-Gly-AMCGly-Gly-AMC
gly-gly-amc, a fluorogenic peptide substrate, facilitates the evaluation of bacterial protease activity in p. aeruginosa and s. aureus [1] [2].
更新時間:2025-09-05
Glycyuralin E；化合物 Glycyuralin EGlycyuralin E
glycyuralin e, a natural product, can be isolated from glycyrrhiza uralensis [1].
更新時間:2025-09-05
Glycyrrhizin-6′′-methylester；化合物 Glycyrrhizin-6′′-methylesterGlycyrrhizin-6′′-methylester
glycyrrhizin-6′′-methylester (compound 22), isolated from licorice root, serves as an aglycone to form methyl glucuronate. this process imparts a characteristic sweet and licorice flavor, devoid of bitterness, highlighting the crucial role of the free carboxyl group on the cone-bound glucuronic acid moiety in contributing to the compound´s natural sweetness and licorice taste [1].
更新時間:2025-09-05
Glycylglycylcysteine；化合物 GlycylglycylcysteineGlycylglycylcysteine
glycylglycylcysteine is an inhibitor of thrombin activatable fibrinolysis inhibitor (tafi), exhibiting a k_i value of 0.99 ?m and an ic_50 of 9.4 ?m in tafi substrate assays. tafi, a basic carboxypeptidase, hinders fibrinolysis by cleaving c-terminal lysine residues on partially degraded fibrin [1].
更新時間:2025-09-05
Glycoside St-J；化合物 Glycoside St-JGlycoside St-J
glycoside st-j (compound 2), a triterpenoid saponin isolated from anemone flaccida, exhibits antitumor activity by inhibiting hela cell proliferation and shows potential for use in the development of novel anticancer agents [1].
更新時間:2025-09-05
Glycoside O-4；化合物 Glycoside O-4Glycoside O-4
glycoside o-4 is a naturally occurring compound.
更新時間:2025-09-05
Glycolate oxidase-IN-1；化合物 Glycolate oxidase-IN-1Glycolate oxidase-IN-1
glycolate oxidase-in-1 (compound 26), a salicylic acid derivative, serves as an inhibitor of glycolate oxidase (go) and exhibits an inhibitory concentration (ic50) of 38.2 μm. it is efficacious in reducing oxalate production in hyperoxaluric hepatocytes and has potential applications in researching primary hyperoxaluria type 1 (ph1) [1].
更新時間:2025-09-05
5,7,3’,4’-Tetramethoxyflavone木犀草素四甲醚木犀草素四甲醚|||3,4,5,7-四甲氧基黃酮
5,7,3´,4´-tetramethoxyflavone (tmf), a prominent polymethoxyflavone (pmf) derived from m. exotica, displays a range of notable bioactivities. these include anti-malarial, anti-fungal, anti-mycobacterial, and anti-inflammatory properties. moreover, tmf specifically targets β-catenin signaling to exhibit chondroprotective activity.
更新時間:2025-09-05
Glycine, N-[(1,1-dimethylethoxy)carbonyl]thio-L-phenylalanyl-, methyl ester；化合物 Glycine, N-[(1,1-dim
glycine, n-[(1,1-dimethylethoxy)carbonyl]thio-l-phenylalanyl-, methyl ester (compound 3b) is a sulfamide-containing polypeptide that can be utilized in the synthesis of peptide-agent coupling compounds [1].
更新時間:2025-09-05
Glutaryl coenzyme A lithium；化合物 Glutaryl coenzyme A lithiumGlutaryl coenzyme A lithium
glutaryl coenzyme a lithium, a derivative of the endogenous metabolite glutaryl coenzyme a, is utilized in experiments related to hmg-coa or glutaryl-coa.
更新時間:2025-09-05
GLUT1-IN-3；化合物 GLUT1-IN-3GLUT1-IN-3
glut1-in-3 (compd 4b), a compound under investigation for type 1 glucose transporter deficiency syndrome, effectively inhibits seizures [1].
更新時間:2025-09-05
GluR23Y；化合物 GluR23YGluR23Y
glur23y, a biologically active peptide, was utilized in an elisa-based cell-surface assay to assess insulin-stimulated endocytosis of native ampa receptors in cultured hippocampal neurons. glur23y effectively inhibited the insulin-induced decrease in receptor presence. the inhibition of insulin effects was achieved by introducing glur23y into neurons through fusion with the membrane transduction domain of hiv-1 tat.
更新時間:2025-09-05
GluN1(359-378)；化合物 GluN1(359-378)GluN1(359-378)
glun1 (359-378) is an antibody targeting the n-methyl-d-aspartate receptor (nmdar) capable of crossing the blood-brain barrier and is utilized in researching therapies for anti-nmdar encephalitis that focus on the immune system [1].
更新時間:2025-09-05
GluN1(356-385)；化合物 GluN1(356-385)GluN1(356-385)
glun1 (356-385) is an antigenic peptide implicated in n-methyl-d-aspartate receptor (nmdar) encephalitis and has been shown to decrease the density of nmdar surface clusters in hippocampal neurons. it serves as a tool to investigate the pathogenesis of anti-nmdar encephalitis [1].
更新時間:2025-09-05
Glucozaluzanin C；化合物 Glucozaluzanin CGlucozaluzanin C
glucozaluzanin c, a lignan extracted from the meoh extract of ainsliaea acerifolia (compositae) roots, demonstrates ed50 values of 2.45 μg/ml for a549 cells, 1.37 μg/ml for sk-ov-3 cells, 0.40 μg/ml for sk-mel-2 cells, 1.41 μg/ml for xf498 cells, and 1.43 μg/ml for hct15 cells, respectively [1].
更新時間:2025-09-05
PNU112455A hydrochloride；化合物PNU 112455APNU 112455A；PNU 112455A
pnu112455a hydrochloride is an atp site competetive inhibitor of cdk2 and cdk5,binds to the atp site of cdk2 and cdk5 with kms of 3.6 and 3.2 μm, respectively.
更新時間:2025-09-05

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