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T10236LACHN-975；化合物 T10236LACHN-975
ACHN-975 is a highly potent and selective LpxC inhibitor, demonstrating subnanomolar inhibitory activity. It effectively targets a broad spectrum of gram-negative bacteria, with low minimum inhibitory concentration (MIC) values (≤1 μg/mL)[1].
价 格：￥电议型 号：T10236L产 地：中国大陆
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T10236ACHN-975 TFA；化合物 T10236ACHN-975 TFA
ACHN-975 TFA is a selective LpxC inhibitor with a subnanomolar inhibitory. It is against a wide range of gram-negative bacterias with low MIC values (≤1 μg/mL).
价 格：￥电议型 号：T10236产 地：中国大陆
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T10229Acebutolol D7；化合物 T10229Acebutolol D7
Acebutolol D7 is a deuterium-labeled Acebutolol. Acebutolol is a selective antagonist of the β1 adrenergic receptor used in the treatment of angina pectoris, hypertension, and cardiac arrhythmias.
价 格：￥电议型 号：T10229产 地：中国大陆
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T10222ABMA；化合物ABMAABMA
ABMA is a broad-spectrum inhibitor of intracellular toxins and pathogens. ABMA efficiently protects cells against various pathogens including viruses, intracellular bacteria, and parasite. ABMA selectively acts at host cell late endosomes rather than targeting toxin or pathogen itself.
价 格：￥电议型 号：T10222产 地：中国大陆
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T10221LAbeprazan；化合物 T10221LDWP14012|||Abeprazan|||DWP-14012|||DWP14012|||DWP 14012|||DWP14012|||Abeprazan；
Abeprazan (DWP14012) is a potassium-competitive acid blocker and it is developed as a potential alternative to proton pump inhibitor for the treatment of acid-related diseases[1]. Abeprazan inhibits H+, K+- ATPase by reversible potassium-competitive ionic binding with no acid activation required.
价 格：￥电议型 号：T10221L产 地：中国大陆
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T10219ABBV-4083；化合物 T10219ABBV-4083
ABBV-4083 is a Tylosin A analog that has potent anti-Wolbachia and anti-filarial activity.
价 格：￥电议型 号：T10219产 地：中国大陆
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T10217LAbarelix；阿巴瑞克R3827|||PPI 149；R3827|||阿巴瑞克|||PPI 149
Abarelix (PPI 149) is a potent gonadotrophin-releasing hormone (GnRH) antagonist, which is used for prostate cancer treatment.
价 格：￥电议型 号：T10217L产 地：中国大陆
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T10209A-887826；化合物 T10209A-887826
A-887826 is a selective, orally bioavailable, and voltage-dependent Na(v1.8) channel blocker (IC50: 11 nM). It attenuates neuropathic tactile allodynia in vivo.
价 格：￥电议型 号：T10209产 地：中国大陆
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T10208A-69412；化合物A-69412N-1-(Fur-3-ylethyl)-N-hydroxyurea；N-1-(Fur-3-ylethyl)-N-hydroxyurea
A-69412 (N-1-(Fur-3-ylethyl)-N-hydroxyurea) is a reversible, specific inhibitor of the hydrophilic 5-lipoxygenase. It has the potential to treat ulcerative colitis and asthma, and possibly other inflammatory and allergic conditions.
价 格：￥电议型 号：T10208产 地：中国大陆
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T10207A 438079；化合物A 438079A 438079
A 438079 is a potent, and selective antagonist of P2X7 receptor (pIC50: 6.9).
价 格：￥电议型 号：T10207产 地：中国大陆
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T10206A 419259；化合物 T10206RK-20449；RK-20449
A 419259 is a pyrrolo-pyrimidine inhibitor, designed to enhance selectivity towards the Src family (IC50s: 9 nM, <3 nM and <3 nM for Src, Lck and Lyn).
价 格：￥电议型 号：T10206产 地：中国大陆
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T10199GNF-PF-3777；化合物GNF-PF-37778-Nitrotryptanthrin；8-Nitrotryptanthrin
GNF-PF-3777 (8-Nitrotryptanthrin) (8-Nitrotryptanthrin) is a potent inhibitor of human indoleamine 2,3-dioxygenase 2 (hIDO2; Ki: 0.97 μM).
价 格：￥电议型 号：T10199产 地：中国大陆
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T101988-M-PDOT；8-甲氧基-2-丙胺四氢萘8-Methoxy-2-propionamidotetralin|||AH-002；8-Methoxy-2-propionamidotetralin|||A
8-M-PDOT (AH-002) is a selective and potent melatonin MT2 receptor agonist that also inhibits MT1 receptors.8-M-PDOT has anxiolytic activity and may be used to study MT2-induced neuropathic pain.
价 格：￥电议型 号：T10198产 地：中国大陆
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T10191L7-Chlorokynurenic acid；7-氯犬尿酸7-chloro-4-hydroxy-2-carboxyquinoline|||7-CKA；7-chloro-4-hydroxy-2-carb
7-Chlorokynurenic acid (7-chloro-4-hydroxy-2-carboxyquinoline) is an effecitve and selective antagonist of NMDA receptor with IC50 of 0.56 μM for the glycine B coagonist site. 7-Chlorokynurenic acid inhibits the reuptake of glutamate into synaptic vesicles with a Ki of 0.59 μM and shows antinociceptive actions after neuraxial delivery.
价 格：￥电议型 号：T10191L产 地：中国大陆
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T101907-BIA；化合物7-BIA7-BIA
7-BIA is a receptor-type protein tyrosine phosphatase D (PTPRD) inhibitor with anti-addictive properties and can be used in the study of neuropathic pain.
价 格：￥电议型 号：T10190产 地：中国大陆
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T101897-[4-(2-Piperidinyl)ethoxy]benzoyl Raloxifene；化合物 T101897-[4-(2-Piperidinyl)ethoxy]benzoyl Raloxifen
7-[4-(2-Piperidinyl)ethoxy]benzoyl Raloxifene is a liver receptor homolog-1 (LRH-1) antagonist (IC50: 3.1 μM).
价 格：￥电议型 号：T10189产 地：中国大陆
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T101806-Alpha Naloxol；化合物 T10180Alpha-Naloxol；Alpha-Naloxol
6-Alpha Naloxol(Alpha-Naloxol) is an opioid antagonist and is a human metabolite of naloxone.
价 格：￥电议型 号：T10180产 地：中国大陆
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T101795β-?Dutasteride；化合物 T101795β-?Dutasteride
5β-Dutasteride is the S configuration of Dutasteride. It is a potent inhibitor of both 5 alpha-reductase isozymes.
价 格：￥电议型 号：T10179产 地：中国大陆
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T101695-HT4 antagonist 1；化合物5-HT4 antagonist 15-HT4 antagonist 1
5-HT4 antagonist 1 is an antagonist of 5-HT4 (pKi = 9.6).
价 格：￥电议型 号：T10169产 地：中国大陆
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T101675-Dehydroepisterol；化合物 T101675-Dehydroepisterol
5-Dehydroepisterol is an episterol derivative with anti-fungal activities. It can be formed by C-5 sterol desaturase and converted into 24-methylenecholesterol by 7-dehydrocholesterol reductase.
价 格：￥电议型 号：T10167产 地：中国大陆
