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T15388GLPG0974；化合物GLPG0974GLPG-0974；GLPG-0974
GLPG0974 is an antagonist of FFA2/GPR43 with IC50 of 9 nM.
价 格：￥电议型 号：T15388产 地：中国大陆
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T15133Dinoprost；地诺前列素Prostaglandin F2a|||PGF2α；Prostaglandin F2a|||PGF2α|||地诺前列素
Dinoprost (Prostaglandin F2a) is a naturally occurring prostaglandin. It is used in medicine to induce labor and as an abortifacient.
价 格：￥电议型 号：T15133产 地：中国大陆
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T14303Alrizomadlin；化合物AlrizomadlinAPG-115|||AA-115；APG-115|||AA-115
Alrizomadlin (APG-115) is an orally active inhibitor of MDM2 with IC50 of 3.8 nM and Ki of 1 nM, respectively[1]. Alrizomadlin blocks the interaction of MDM2 and p53 and induces cell-cycle arrest and apoptosis in a p53-dependent manner.
价 格：￥电议型 号：T14303产 地：中国大陆
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T13831Prostaglandin D2；前列腺素D2PGD2；PGD2
Prostaglandin D2 (PGD2) is one of the major PGs actively produced in the brain of various mammals,and is a potent endogenous sleep promoting substances.
价 格：￥电议型 号：T13831产 地：中国大陆
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T13705GLPG2451；化合物 T13705GLPG2451
GLPG2451 is a cystic fibrosis transmembrane conductance regulator (CFTR) potentiator. It effectively potentiates low temperature rescued F508del CFTR (EC50: 11.1 nM).
价 格：￥电议型 号：T13705产 地：中国大陆
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T13704GLPG-3221；化合物 T13704GLPG-3221
GLPG-3221 can be uesd for the treatment of cystic fibrosis.GLPG-3221 is a potent, orally active corrector of CFTR (cystic fibrosis transmembrane conductance regulator), with an EC50 of 105 nM.
价 格：￥电议型 号：T13704产 地：中国大陆
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T13452(S)-MCPG化合物 T13452(+)-MCPG
(S)-MCPG is the active isomer of (RS)-MCPG, non-selective group I/group II metabotropic glutamate receptor antagonist.
价 格：￥电议型 号：T13452产 地：中国大陆
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T12440PGAM1-IN-2；化合物 T12440PGAM1-IN-2
PGAM1-IN-2 is an inhibitor of phosphoglycerate mutase 1 ( PGAM1 ) with an IC 50 of 2.1 μM [1].
价 格：￥电议型 号：T12440产 地：中国大陆
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T12439PGAM1-IN-1；化合物 T12439PGAM1-IN-1
PGAM1-IN-1 is an inhibitor of phosphoglycerate mutase 1 ( PGAM1 ) with an IC 50 of 6.4 μM [1].
价 格：￥电议型 号：T12439产 地：中国大陆
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T12100mPGES1-IN-3；化合物 T12100mPGES1-IN-3
mPGES1-IN-3 is a potent and selective inhibitor of microsomal prostaglandin E2 synthase-1 (mPGES-1) .
价 格：￥电议型 号：T12100产 地：中国大陆
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T11411GLPG1205；化合物GLPG1205GLPG1205
GLPG1205 is a potent, orally active GPR84 (G protein-coupled receptor) antagonist with anti-inflammatory activity. GLPG1205 shows good PK/PD characteristics and can be used to study pulmonary fibrosis.
价 格：￥电议型 号：T11411产 地：中国大陆
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T11410LGLPG0492；化合物GLPG0492GLPG0492
GLPG0492 is a novel selective androgen receptor modulator. After oral dosing, it showed anabolic activity on muscle, strongly dissociated from the androgenic activity on the prostate.
价 格：￥电议型 号：T11410L产 地：中国大陆
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T11410GLPG0492 (R enantiomer)；化合物 T11410GLPG0492 R enantiomer；GLPG0492 R enantiomer
GLPG0492 R enantiomer is the R enantiomer of GLPG-0492, a novel selective androgen receptor modulator.
价 格：￥电议型 号：T11410产 地：中国大陆
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T11032DHPG；DL-Α-(3,5-二羟基苯基)甘氨酸(RS)-3,5-DHPG；(RS)-3,5-DHPG|||DL-Α-(3,5-二羟基苯基)甘氨酸
DHPG ((RS)-3,5-DHPG) ((RS)-3,5-DHPG) is an effective antagonist of mGluR linked to phospholipase D. It is an amino acid that can be used as a selective and potent agonist for Group I mGluR (mGluR 1 and mGluR 5) and has no effect on Group II or Group III mGluRs .
价 格：￥电议型 号：T11032产 地：中国大陆
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T10809LCHPG hydrochloride；化合物CHPG盐酸盐CHPG hydrochloride(170846-74-9 Free base)；CHPG hydrochloride(170846-74-
CHPG hydrochloride is a selective agonist of mGluR5.
价 格：￥电议型 号：T10809L产 地：中国大陆
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T10808CHPG sodium salt；CHPG钠盐CHPG sodium salt
CHPG sodium salt is a selective agonist of mGluR5 and activates the ERK and Akt signaling pathways. CHPG sodium salt can be used in studies about traumatic brain injury.
价 格：￥电议型 号：T10808产 地：中国大陆
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T10678Carboxypeptidase G2 (CPG2) Inhibitor；羧肽酶G2抑制剂CPG2 Inhibitor|||Carboxypeptidase G2 Inhibitor；CPG2 Inh
Carboxypeptidase G2 (CPG2) Inhibitor (CPG2 Inhibitor) is a new CPG2 Inhibitor with antitumor activity.
价 格：￥电议型 号：T10678产 地：中国大陆
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T10673Carbacyclin；化合物 T10673Carbaprostacyclin|||Carba-PGI2；Carbaprostacyclin|||Carba-PGI2
Carbacyclin, a PGI2 analog, is a prostacyclin (PGI2) receptor agonist and vasodilator with potent inhibitory platelet aggregation.
价 格：￥电议型 号：T10673产 地：中国大陆
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T10483Lisaftoclax；化合物LisaftoclaxBcl-2/Bcl-xl inhibitor 1|||APG-2575；Bcl-2/Bcl-xl inhibitor 1|||APG-2575
Lisaftoclax (Bcl-2/Bcl-xl inhibitor 1) is an oral dual inhibitor of Bcl-2 and Bcl-xl, with IC50 values of 2 nM and 5.9 nM for Bcl-2 and Bcl-xl, respectively. Lisaftoclax is used to treat chronic lymphocytic leukemia (CLL) by inhibiting the action of the BCL-2 protein, which promotes the death of leukemia cells.
价 格：￥电议型 号：T10483产 地：中国大陆
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T10098PGS-IN-1；化合物PGS-IN-1KME-4；KME-4
PGS-IN-1 (KME-4) is a potent inhibitor of prostaglandin synthetase (PGS, IC50: 0.28 μM) and 5-lipoxygenase (IC50: 1.05 μM).
价 格：￥电议型 号：T10098产 地：中国大陆
