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T134923,5-Diiodothyropropionic acid3,5-二碘甲腺丙酸；Ditpa cpd；C082182
3,5-Diiodothyropropionic acid is a thyroid hormone analog. It induces α-myosin heavy chain mRNA expression, binds to thyroid hormone receptor (Ka: 2.40/M and 4.06/M for TRα1 and TRβ1).
价 格：￥电议型 号：T13492产 地：中国大陆
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T13381Z433927330
Z433927330 is a potent and selective Aquaporin-7 (AQP7) inhibitor(IC50s of 0.2).
价 格：￥电议型 号：T13381产 地：中国大陆
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T13316VU0134992 hydrochloride
VU0134992 hydrochloride is the first subtype-preferring, orally active and selective blocker of Kir4.1 potassium channel pore(IC50 : 0.97 μM).
价 格：￥电议型 号：T13316产 地：中国大陆
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T13112L1Tat-NR2B9c acetateNA-1 acetate；Tat-NR2B9c acetate (500992-11-0 Free base)
Tat-NR2B9c acetate is a postsynaptic density-95 (PSD-95) inhibitor, with EC50 values of 6.7 nM and 670 nM for PSD-95d2 (PSD-95 PDZ domain 2) and PSD-95d1, respectively. Tat-NR2B9c acetate disrupts the PSD-95/NMDAR interaction, inhibiting NR2A and NR2B bin
价 格：￥电议型 号：T13112L1产 地：中国大陆
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T13092Tauro-Obeticholic acid
Tauro-Obeticholic acid is an active Obeticholic acid metabolite. Obeticholic acid is an orally bioavailable agonist of farnesoid-X receptor (FXR).
价 格：￥电议型 号：T13092产 地：中国大陆
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T13063T6167923
T6167923 is a potent and selective MyD88-dependent signaling pathways inhibitor.
价 格：￥电议型 号：T13063产 地：中国大陆
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T13016SR59230A
SR59230A is a potent, selective antagonist of β3-adrenergic receptor(β3, β1, and β2 receptors with IC50s of 40, 408, and 648 nM , respectively).
价 格：￥电议型 号：T13016产 地：中国大陆
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T12929SKF-34288 hydrochloride3-Mercaptopicolinic acid hydrochloride；3 - 巯基吡啶甲酸
SKF-34288 hydrochloride is an inhibitor of phosphoenolpyruvate carboxykinase (PEPCK),and inhibits Asn metabolism and results in an increase in amino acids and amides.
价 格：￥电议型 号：T12929产 地：中国大陆
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T12928SK33
SK33 is a potent and tissue selective anti-androgen agent. SK33 reduces androgen receptor (AR) transcriptional activity.
价 格：￥电议型 号：T12928产 地：中国大陆
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T1292Tiapride hydrochloride
Tiapride is a selective blocker of D2/3 dopamine receptors in the brain. It is used in the therapy of various psychiatric and neurological disorders containing dyskinesia, negative symptoms of psychosis, alcohol withdrawal syndrome, and aggression and agi
价 格：￥电议型 号：T1292产 地：中国大陆
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T12882LSetmelanotide Acetate(920014-72-8 free base)BIM-22493 Acetate；RM-493 Acetate；IRC-022493 Acetate
Setmelanotide Acetate is a selective agonist of melanocortin 4 receptor (MC4R)(human and rat MC4R with EC50s of 0.27 nM and 0.28 nM, respectively).
价 格：￥电议型 号：T12882L产 地：中国大陆
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T12877LSeltorexantJNJ-42847922
Seltorexant crosses the blood-brain barrier and quickly occupies OX2R binding sites in the rat brain. Seltorexant is a high-affinity and selective orexin-2 receptor antagonist (pKi: 8.0 and 8.1 for human and rat OX2R).
价 格：￥电议型 号：T12877L产 地：中国大陆
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T12492PivagabineCXB-722；匹伐加宾
Pivagabine is a derivative of hydrophobic 4-aminobutyric acid, with neuromodulatory activity. Pivagabine penetrates the blood-brain barrier in rats. Pivagabine antagonizes the effects of foot shock on both GABAA receptor function and corticotropin-releasi
价 格：￥电议型 号：T12492产 地：中国大陆
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T12437PF429242 dihydrochloride
PF429242 dihydrochloride can reversibly inhibit S1P (IC50 of 175 nM).
价 格：￥电议型 号：T12437产 地：中国大陆
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T12432PF-06928215
PF-06928215 is an inhibitor of cGAS (cyclic GMP-AMP Synthase) (IC50 of 4.9 μΜ).
价 格：￥电议型 号：T12432产 地：中国大陆
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T12192NCGC00229600
NCGC00229600 is an allosteric inverse thyrotropin receptor (TSHR) agonist. NCGC00229600 inhibits both TSH and stimulating antibody activation of TSHRs endogenously and can be used in Graves´ disease studies.
价 格：￥电议型 号：T12192产 地：中国大陆
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T1215Nicardipine hydrochlorideYC-93 Hydrochloride；Nicardipine HCl；RS-69216；盐酸尼卡地平
Nicardipine Hydrochloride is the hydrochloride salt form of nicardipine, a synthetic derivative of nitrophenyl-pyridine and potent calcium channel blocker, Nicardipine (Nifedipine Family) blocks calcium ions from certain cell walls and inhibits contractio
价 格：￥电议型 号：T1215产 地：中国大陆
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T12092Monacolin J辛伐他汀内酯二醇；Lovastatin diol lactone；Antibiotic MB 530A
Monacolin J is a cholesterol biosynthesis inhibitor.
价 格：￥电议型 号：T12092产 地：中国大陆
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T11929M2N12
M2N12 is a potent and highly selective inhibitor of cell division cycle 25C protein phosphatase (Cdc25C, IC50 = 0.09 μM). M2N12 has anti-tumor activity. M2N12 also has promising activity against Cdc25A(IC50 = 0.53? μM) and Cdc25B(IC50 = 1.39 μM).
价 格：￥电议型 号：T11929产 地：中国大陆
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T11925M?89
M-89 inhibits the menin-mixed lineage leukemia (Menin-MLL) protein-protein interaction and has potential to treat MLL leukemia. M-89 is a highly potent and specific menin inhibitor, with a Kd of 1.4 nM for binding to menin.
价 格：￥电议型 号：T11925产 地：中国大陆
