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T74070NHC-triphosphate tetrasodium；化合物 NHC-triphosphate tetrasodiumNHC-triphosphate tetrasodium
NHC-triphosphate tetrasodium, the active phosphorylated intracellular metabolite of β-d-N4-Hydroxycytidine (NHC) in its triphosphate form, functions as a weak alternative substrate for viral polymerase, allowing its incorporation into HCV replicon RNA.
价 格：￥电议型 号：T74070产 地：中国大陆
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T7401(S)-3-AMino-2-Methylpropanoic acid-HCl；化合物T7401(S)-3-AMino-2-Methylpropanoic acid-HCl
(S)-3-AMino-2-Methylpropanoic acid-HCl is an amino acid derivative that can be an agonist of the excitatory neurotransmitter glutamate and affect the nervous system.
价 格：￥电议型 号：T7401产 地：中国大陆
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T73716Miglustat-d9 HCl；化合物 Miglustat-d9 HClMiglustat-d9 HCl
Miglustat-d9 (hydrochloride), a deuterium-labeled variant of Miglustat (hydrochloride), functions as a glucosylceramide synthase inhibitor. Its primary application is in the treatment of Type I Gaucher disease (GD1) [1][2].
价 格：￥电议型 号：T73716产 地：中国大陆
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T73400LPG-11047 2HCl；PG-11047二盐酸盐PG-11047 2HCl(949933-50-0 Free base)|||CGC-11047 2HCl；PG-11047 2HCl(949933
PG-11047 2HCl is an apoptosis-stimulating agent used in the treatment of genitourinary disorders, immune system disorders, genetic disorders and malformations, ocular disorders, and disorders of the blood and lymphatic systems, and in the study of lymphomas and prostate cancer.
价 格：￥电议型 号：T73400L产 地：中国大陆
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T73336Ketotifen；化合物 KetotifenHC 20-511；酮替芬|||HC 20-511
Ketotifen (HC 20-511) is a second-generation, orally active noncompetitive histamine 1 (H1) receptor antagonist and mast cell stabilizer. It inhibits 6-phosphogluconate dehydrogenase (PGD) in vitro and displays antiviral activity against SARS-CoV-2 and the Influenza virus. Additionally, Ketotifen is utilized in researching autoimmune encephalomyelitis (EAE) and preventing asthma attacks.
价 格：￥电议型 号：T73336产 地：中国大陆
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T73177hCAII-IN-9；化合物hCAII-IN-9hCAII-IN-9
hCAII-IN-9 is a potent carbonic anhydrase inhibitor that inhibits hCA II, hCA IX, and hCA XII with IC50s of 1.18 μM and 0.17 μM , and 2.99 μM , respectively. hCAII-IN-9 is not blood-brain barrier permeable.
价 格：￥电议型 号：T73177产 地：中国大陆
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T73036hCA IX-IN-2；化合物 hCA IX-IN-2hCA IX-IN-2
hCA IX-IN-2 is a highly potent and selective inhibitor of hCA IX, exhibiting an inhibition constant (K I) value of 32.1 nM and demonstrating anti-proliferative activity.
价 格：￥电议型 号：T73036产 地：中国大陆
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T73030hCAIX-IN-14；化合物 hCAIX-IN-14hCAIX-IN-14
hCAIX-IN-14 is a potent inhibitor of human CA IX with a K i value of 134.8 nM [1] .
价 格：￥电议型 号：T73030产 地：中国大陆
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T73029hCAIX-IN-15；化合物 hCAIX-IN-15hCAIX-IN-15
hCAIX-IN-15 is a potent inhibitor of human carbonic anhydrase IX (hCA IX) with an inhibition constant (Ki) of 38.8 nM, exhibiting broad-spectrum anticancer activity suitable for cancer research [1].
价 格：￥电议型 号：T73029产 地：中国大陆
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T73028hCAIX-IN-16；化合物 hCAIX-IN-16hCAIX-IN-16
hCAIX-IN-16 (Compound 12d), an inhibitor of hCA IX, exhibits inhibition constants (K i) of 190.0 nM for hCA IX and 187.9 nM for hCA XII. It can arrest the cell cycle in the G0-G1 and S phases and induce apoptosis in MDA-MB-468 breast cancer cells. Demonstrating broad-spectrum anticancer activity, hCAIX-IN-16 is a potential tool for cancer research [1].
价 格：￥电议型 号：T73028产 地：中国大陆
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T72840hCAIX/XII-IN-6；化合物 hCAIX/XII-IN-6hCAIX/XII-IN-6
hCAIX/XII-IN-6, an orally active carbonic anhydrase (CA) inhibitor, targets human CA isoforms hCA I, II, IV, IX, and XII with inhibition constants (K i) of 6697 nM, 2950 nM, 4093 nM, 4.1 nM, and 7.7 nM, respectively. This compound is utilized in rheumatoid arthritis (RA) research.
价 格：￥电议型 号：T72840产 地：中国大陆
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T72784LOTUB1/USP8-IN-1 HCl；OTUB1/USP8抑制剂1盐酸盐OTUB1/USP8-IN-1 HCl（2858800-98-1 Free base）；OTUB1/USP8-IN-1 HCl
OTUB1/USP8-IN-1 HCL is a potent dual inhibitor of OTUB1 and USP8 with potential antitumour activity, inhibiting both OTUB1 and USP8. OTUB1/USP8-IN-1 may be used in the study of leukaemia.
价 格：￥电议型 号：T72784L产 地：中国大陆
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T72283(+)-Dihydrocalanolide A；化合物 (+)-Dihydrocalanolide ANSC 678323|||DHCal A ; NSC 678323|||DHCal A；NSC
(+)-Dihydrocalanolide A (DHCal A; NSC 678323), an orally active nonnucleoside inhibitor of reverse transcriptase, is utilized in research related to HIV infection.
价 格：￥电议型 号：T72283产 地：中国大陆
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T72058LCDD-1102 HCl；CDD-1102盐酸盐CDD-1102 HCl(2757619-84-2 Free base)；CDD-1102 HCl(2757619-84-2 Free base)
CDD-1102 HCl is a novel BRDT-BD4 / BRD2-BD1302 selective inhibitor that shows non-hormonal contraceptive potential in ex vivo experiments.
价 格：￥电议型 号：T72058L产 地：中国大陆
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T72014BZL-HIS-OME 2HCL；化合物 BZL-HIS-OME 2HCLBZL-HIS-OME 2HCL
BZL-HIS-OME 2HCL is the dihydrochloride salt of BZL-HIS-OME, a sweet almond and yeast β-glucosidase inhibitor.
价 格：￥电议型 号：T72014产 地：中国大陆
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T71989CPD7 HCl；化合物 CPD7 HClCPD7 HCl
CPD7 HCl is a novel non-RBD binding modulator to inhibit SARS-CoV-2 by prohibiting the conformational change of the spike (S) protein.
价 格：￥电议型 号：T71989产 地：中国大陆
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T71982Ofloxacin HCl；化合物 Ofloxacin HClOfloxacin HCl
Ofloxacin HCl is a synthetic fluoroquinolone ( FLUOROQUINOLONES) antibacterial agent that inhibits the supercoiling activity of bacterial DNA GYRASE, halting DNA REPLICATION.
价 格：￥电议型 号：T71982产 地：中国大陆
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T7197LFadrozole HCl hydrate；化合物 T7197LFadrozole|||CGS-16949A|||Fadrozole hydrochloride hemihydrate|||CGS16
Fadrozole is a selective inhibitor of aromatase. It also effective in the treatment of estrogen-dependent diseases including breast cancer.
价 格：￥电议型 号：T7197L产 地：中国大陆
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T71964Ravidasvir HCl；化合物 Ravidasvir HClRavidasvir HCl
Ravidasvir, also known as PPI-668 and ASC16, is a second-generation, orally active, potent and selective HCV NS5A protein inhibitor.
价 格：￥电议型 号：T71964产 地：中国大陆
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T71962DAU 5884 HCl；化合物 DAU 5884 HClDAU 5884 HCl
DAU 5884 HCl is an M3 receptor antagonist
价 格：￥电议型 号：T71962产 地：中国大陆
