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T15459H2N-PEG2-CH2COOH；化合物 T15459H2N-PEG2-CH2COOH
H2N-PEG2-CH2COOH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15459产 地：中国大陆
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T15457LH-Lys-Trp-Lys-OH acetate；化合物 H-Lys-Trp-Lys-OH acetateH-Lys-Trp-Lys-OH acetate(38579-27-0 free base)；
H-Lys-Trp-Lys-OH acetate is a peptide with antibacterial and antiviral activities.
价 格：￥电议型 号：T15457L产 地：中国大陆
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T15457H-Lys-Trp-Lys-OH；化合物 T15457H-Lys-Trp-Lys-OH
H-Lys-Trp-Lys-OH is a small molecule peptide that shows antibacterial and antiviral activities.
价 格：￥电议型 号：T15457产 地：中国大陆
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T15456GYKI 53655 hydrochlorideGYKI 53655 盐酸盐GYKI53655 hydrochloride|||LY300168 hydrochloride
GYKI 53655 hydrochloride (LY300168 hydrochloride) is an antagonist of AMPA and is used in the study of neurological disorders.
价 格：￥电议型 号：T15456产 地：中国大陆
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T15455RGH-5526；化合物 T15455GYKI-11679；GYKI-11679
RGH-5526 is a novel antihypertensive drug. It causes an increase in hypothalamic norepinephrine (NA) turnover (utilization), and the increase in hypothalamic noradrenergic neuron activity may lead to a decrease in peripheral sympathetic nerve activity, resulting in a significant reduction in blood pressure.
价 格：￥电议型 号：T15455产 地：中国大陆
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T15454GW843682X；化合物GW843682XGW843682；GW843682
GW843682X (GW843682) is a selective and ATP-competitive inhibitor of PLK1 and PLK3 (IC50s = 2.2 nM and 9.1 nM).
价 格：￥电议型 号：T15454产 地：中国大陆
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T15453GW7647化合物GW76472-[[4-[2-[[环己基氨基)羰基](4-环己基丁基)氨基]乙基]苯基]硫基]-2-甲基丙酸
GW7647 is a potent agonist of PPARα (EC50s: 6 nM, 1.1 μM, and 6.2 μM for human PPARα, PPARγ, and PPARδ, respectively).
价 格：￥电议型 号：T15453产 地：中国大陆
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T15452GW7604；化合物 T15452GW7604
GW7604 is an antiestrogen and it also is the metabolite of GW5638. GW5638 is an antagonist of high-affinity estrogen receptor (ER).
价 格：￥电议型 号：T15452产 地：中国大陆
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T15451GW-870086；化合物GW-870086GW-870086
GW-870086 is an effective anti-inflammatory agent. GW-870086 also plays a role in a glucocorticoid receptor agonist (pIC50: 10.1 in A549 cells expressing NF-κB).
价 格：￥电议型 号：T15451产 地：中国大陆
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T15450GW-803430；化合物 T15450GW-3430；GW-3430
GW-803430 is a potent and selective antagonist of melanin-concentrating hormone receptor 1 (MCH R1) (pIC50: 9.3). GW-803430 is orally active in an animal model of obesity.
价 格：￥电议型 号：T15450产 地：中国大陆
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T1545Levamlodipine；左旋氨氯地平(S)-Amlodipine|||S-amlodipine；左旋氨氯地平|||(S)-Amlodipine|||S-amlodipine
Levamlodipine (S-amlodipine) belongs to the dihydropyridine group of calcium channel blockers. Levamlodipine, also known as S-amlodipine, is a pharmacologically active enantiomer of amlodipine, an antihypertensive and anti-anginal medication. The names S-amlodipine and levamlodipine may be used interchangeably as both substances are the same, however, with differing nomenclature. As a racemic mixture, amlodipine contains (R) and (S)-amlodipine isomers, but only (S)-amlodipine as the active moiet
价 格：￥电议型 号：T1545产 地：中国大陆
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T15449GW-406381化合物 T15449GW406381|||GW 406381
GW406381 is a highly selective inhibitor of cyclooxygenase-2 (COX-2). GW406381 also attenuates spontaneous ectopic discharge in the sural nerves of rats following chronic constriction injury.
价 格：￥电议型 号：T15449产 地：中国大陆
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T15448GW-1100；化合物 T15448GW-1100
GW-1100 is a selective antagonist of GPR40 (pIC50: 6.9). GW1100 also plays the role of a GPR40 inverse agonist.
价 格：￥电议型 号：T15448产 地：中国大陆
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T15447Guacetisal；呱西替柳Guacetisal
Guacetisal is extracted from the esterification reaction of acetylsalicylic acid with guaiacol which can be used for research on the treatment of chronic bronchitis.
价 格：￥电议型 号：T15447产 地：中国大陆
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T15446GT 949；化合物GT 949GT 949
GT 949 is a selective excitatory positive allosteric modulator of amino acid transporter-2 (EAAT2) (EC50: 0.26 nM).
价 格：￥电议型 号：T15446产 地：中国大陆
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T15444GSK962；化合物GSK962GSK962
GSK962 is a GSK963 inactive enantiomer. It can be used to confirm the on-target effects.
价 格：￥电议型 号：T15444产 地：中国大陆
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T15443GSK8814；化合物 T15443GSK8814
GSK8814 is a selective and ATAD2/2B bromodomain chemical probe and inhibitor (binding constant pKd=8.1 and a pKi=8.9 in BROMOscan). GSK8814 displays 500-fold selectivity for ATAD2 over BRD4 BD1. GSK8814 binds to ATAD2 and BRD4 BD1 (pIC50s: 7.3 and 4.6).
价 格：￥电议型 号：T15443产 地：中国大陆
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T15442GSK864；化合物 T15442GSK864
GSK864 is an inhibitor of isocitrate dehydrogenase 1 (IDH1) mutant. GSK864 inhibits IDH1 mutants R132C, R132H, and R132G (IC50: 8.8, 15.2, and 16.6 nM).
价 格：￥电议型 号：T15442产 地：中国大陆
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T15441GSK8573；化合物GSK8573GSK8573
GSK8573 is an inactive control compound for GSK2801. GSK8573 has binding activity to BRD9 (Kd of 1.04 μM).
价 格：￥电议型 号：T15441产 地：中国大陆
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T15440GSK376501A；化合物GSK376501AGSK376501A
GSK376501A is a selective and effective modulator of peroxisome proliferator-activated receptor γ (PPARγ) for the study of type 2 diabetes.
价 格：￥电议型 号：T15440产 地：中国大陆
