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T1555Diclofenac sodium双氯芬酸钠；GP 45840
Diclofenac sodium is a non-steroidal anti-inflammatory agent (NSAID) with antipyretic and analgesic actions. It is primarily available as the sodium salt.
价 格：￥电议型 号：T1555产 地：中国大陆
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T15370GANT 58NSC 75503；4,44乔,4乔(2,3,4,5-Thiophentetrayl)tetrakis-pyridine
GANT 58 is a potent antagonist of Gli. Which inhibits GLI1-induced transcription (IC50: 5 μM).
价 格：￥电议型 号：T15370产 地：中国大陆
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T15261Evocalcet伊万卡赛；KHK7580
Evocalcet has an activating effect on the calcium-sensing receptor (CaSR).
价 格：￥电议型 号：T15261产 地：中国大陆
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T15090DecoglurantRO4995819
Decoglurant is a negative allosteric modulator of mGluR2 and mGluR3 and it also is developed as an antidepressant.
价 格：￥电议型 号：T15090产 地：中国大陆
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T15058DBCO-amine
DBCO-amine is a cleavable ADC linker used in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15058产 地：中国大陆
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T1492Gemifloxacin mesylate甲磺酸吉米沙星；SB-265805S；LB-20304a；Gemifloxacin?mesylate
Gemifloxacin mesylate inhibits activities of DNA gyrase and topoisomerase IV, thereby inhibiting DNA replication and eventually bacterial growth. Gemifloxacin Mesylate is the mesylate salt form of gemifloxacin, a synthetic broad-spectrum fluoroquinolone w
价 格：￥电议型 号：T1492产 地：中国大陆
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T14884CBR-5884
CBR-5884 is an selective, active of phosphoglycerate dehydrogenase (PHGDH) inhibitor with an IC50 of 33 μM. CBR-5884 inhibits de novo serine synthesis in cancer cells and is selectively toxic to cancer cell lines with high serine biosynthetic activity. C
价 格：￥电议型 号：T14884产 地：中国大陆
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T14871Carboxyamidotriazole OrotateL-651582 Orotate；CAI Orotate
Carboxyamidotriazole Orotate is a cytostatic inhibitor of nonvoltage-operated calcium channels and calcium channel-mediated signaling pathways. Carboxyamidotriazole Orotate (L-651582 Orotate) is the orotate salt form of Carboxyamidotriazole (CAI), an oral
价 格：￥电议型 号：T14871产 地：中国大陆
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T14858Calicheamicin卡奇霉素；Calicheamicin γ1
Calicheamicin is an antitumor antibiotic and is a DNA synthesis inhibitor. It also is a cytotoxic agent that causes double-strand DNA breaks.
价 格：￥电议型 号：T14858产 地：中国大陆
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T14685BMS-986158
BMS-986158 is a potent BET inhibitor with IC50s of 6.6 and 5 nM in NCI-H211 small cell lung cancer (SCLC) cells and MDA-MB231 triple negative breast cancer (TNBC) cells, respectively.
价 格：￥电议型 号：T14685产 地：中国大陆
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T14589Biotin-PEG3-acid18-[(3AS,4S,6AR)-六氢-2-氧代-1H-噻吩并[3,4-D]咪唑-4-基]-14-氧代-4,7,10-三氧杂-13-氮杂十八烷酸
Biotin-PEG3-acid is a biotin-labeled, PEG-based PROTAC linker that can be used in the synthesis of PROTACs.Biotin-PEG3-acid is a heterobiofunctional biotin PEG derivative containing a carboxylic acid group. The hydrophilic PEG spacer arm imparts water sol
价 格：￥电议型 号：T14589产 地：中国大陆
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T1458Epalrestat依帕斯他；依帕司他；ONO2235
Epalrestat, an aldose reductase inhibitor, is well tolerated in Long-term therapy. It can effectually ameliorate the associated symptoms of diabetic neuropathy and delay the progression of the disease, particularly in patients with limited microangiopathy
价 格：￥电议型 号：T1458产 地：中国大陆
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T1438Butoconazole nitrate硝酸布康唑；RS 35887
Butoconazole Nitrate is the nitrate salt form of butoconazole, a synthetic imidazole derivative with fungistatic properties. Butoconazole nitrate interferes with steroid biosynthesis by inhibiting the conversion of lanosterol to ergosterol, thereby changi
价 格：￥电议型 号：T1438产 地：中国大陆
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T14378LAZD5582 acetate (1258392-53-8 free base)
AZD5582 acetate is an inhibitor of IAPs, which binds to the BIR3 domains cIAP1, cIAP2, and XIAP with IC50s of 15, 21, and 15 nM, respectively. AZD5582 induces apoptosis.
价 格：￥电议型 号：T14378L产 地：中国大陆
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T14358AvoralstatAVORALSTAT；BCX4161
Avoralstat is an oral plasma kallikrein (PKK) inhibitor. Which is used for the treatment of hereditary angioedema.
价 格：￥电议型 号：T14358产 地：中国大陆
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T14324Artemisone青蒿酮；Artemifone；BAY 44-9585
Artemisone is a potent and semi-synthetic antimalarial, inhibits P. falciparum strains (IC50: 0.83 nM). It also is a potent inhibitor of human CMV.
价 格：￥电议型 号：T14324产 地：中国大陆
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T14316AR-C155858
AR-C155858 is an inhibitor of monocarboxylate transporter MCT1 and MCT2 (Kis: 2.3 nM and 10 nM).
价 格：￥电议型 号：T14316产 地：中国大陆
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T13974ZL0580
ZL0580 induces HIV suppression by inhibiting Tat transactivation and transcription elongation as well as by inducing repressive chromatin structure at the HIV promoter.
价 格：￥电议型 号：T13974产 地：中国大陆
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T1388Fluconazole氟康唑；UK-49858
Triazole antifungal agent that is used to treat oropharyngeal candidiasis and cryptococcal meningitis in AIDS.
价 格：￥电议型 号：T1388产 地：中国大陆
