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T11597LIACS-9571 Hydrochloride (1800477-30-8 free base)；化合物 T11597LIACS-9571 Hydrochloride|||ASIS-P040 Hydr
IACS-9571 Hydrochloride is a selective and potent inhibitor of TRIM24 and BRPF1, (IC50: 8 nM for TRIM24; Kds: 31 nM and 14 nM for TRIM24 and BRPF1).
价 格：￥电议型 号：T11597L产 地：中国大陆
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T11597IACS-9571；化合物 T11597ASIS-P040；ASIS-P040
IACS-9571 is a selective and potent inhibitor of TRIM24 and BRPF1, (IC50: 8 nM for TRIM24; Kds: 31 nM and 14 nM for TRIM24 and BRPF1).
价 格：￥电议型 号：T11597产 地：中国大陆
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T11596IACS-8803；化合物 T11596IACS-8803
IACS-8803 is a potent cyclic dinucleotide STING agonist that exhibits strong systemic antitumor efficacy.
价 格：￥电议型 号：T11596产 地：中国大陆
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T11595IACS-8779；化合物 T11595IACS-8779
IACS-8779 is a potent STING agonist that efficiently stimulates interferon gene activity and exhibits strong systemic antitumor effects.
价 格：￥电议型 号：T11595产 地：中国大陆
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T1159Leflunomide来氟米特SU101|||RS-34821|||HWA486|||来氟米特
Leflunomide (HWA486) is an immunomodulatory agent used in the therapy of rheumatoid arthritis and psoriatic arthritis.
价 格：￥电议型 号：T1159产 地：中国大陆
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T11533Z-HA155；化合物Z-HA155CS-963；CS-963
Z-HA155 (CS-963) selectively and potently inhibits autotaxin with an IC50 of 5.7 nM.
价 格：￥电议型 号：T11533产 地：中国大陆
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T11527LH-Ser-His-OH acetate；化合物H-Ser-His-OH acetateH-Ser-His-OH acetate
H-Ser-His-OH acetate is an endogenous metabolite hydrolysis cleavage activity.
价 格：￥电议型 号：T11527L产 地：中国大陆
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T11527H-Ser-His-OH；化合物 T11527H-Ser-His-OH
H-Ser-His-OH, an endogenous metabolite, is a short peptide with hydrolysis cleavage activity.
价 格：￥电议型 号：T11527产 地：中国大陆
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T11494GSK3532795；化合物 T11494BMS-955176；BMS-955176
GSK3532795 is a potent, orally active, second-generation HIV-1 maturation inhibitor (EC50s: 10.2, 1.9, 2.7, and 13 nM for HIV-1 WT(human serum), HIV-1 WT, HIV-1 V370A, and HIV-1 ΔV370).
价 格：￥电议型 号：T11494产 地：中国大陆
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T11465Lenacapavir；化合物LenacapavirGS-6207；GS-6207
Lenacapavir (GS-6207) is a potent capsid-targeting inhibitor of HIV replication. Lenacapavir shows anti-HIV activity with an EC50 of 100 pM in MT-4 cells.
价 格：￥电议型 号：T11465产 地：中国大陆
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T11434GlyRS-IN-1；化合物 T11434GlyRS-IN-1
GlyRS-IN-1 is an inhibitor of glycyl-tRNA synthase (GlyRS). It can inhibit the growth of bacteria.
价 格：￥电议型 号：T11434产 地：中国大陆
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T11416Glucagon receptor antagonists-5；化合物 T11416Glucagon receptor antagonists-5
Glucagon receptor antagonists-5 is an orally bioavailable indazole-based glucagon receptor antagonist (Ki: 32 nM). It has potential for the treatment of type 2 diabetes mellitus (T2DM).
价 格：￥电议型 号：T11416产 地：中国大陆
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T11415Glucagon receptor antagonists-3；化合物 T11415Glucagon receptor antagonists-3
Glucagon receptor antagonist -3 is a highly effective glucagon receptor antagonist.
价 格：￥电议型 号：T11415产 地：中国大陆
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T11414Glucagon receptor antagonists-2；化合物 T11414Glucagon receptor antagonists-2
Glucagon receptor antagonist -2 is a highly effective glucagon receptor antagonist.
价 格：￥电议型 号：T11414产 地：中国大陆
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T11413Glucagon receptor antagonists-1；化合物 T11413Glucagon receptor antagonists-1
Glucagon receptor antagonist -1 is a highly effective glucagon receptor antagonist.
价 格：￥电议型 号：T11413产 地：中国大陆
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T11378GDC-0834 S-enantiomer；化合物 T11378GDC-0834 S-enantiomer
GDC-0834, the S-enantiomer, is a potent and selective inhibitor of Bruton´s tyrosine kinase (BTK).
价 格：￥电议型 号：T11378产 地：中国大陆
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T1129Benfotiamine苯磷硫胺Benzoylthiamine monophosphate|||S-Benzoylthiamine O-monophosphate|||苯磷硫胺
Benfotiamine (S-Benzoylthiamine O-monophosphate) is a synthetic S-acyl derivative of thiamine (vitamin B1), used as an antioxidant dietary supplement.
价 格：￥电议型 号：T1129产 地：中国大陆
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T1128L(S)-Oxiracetam；化合物 T1128L(S)-ISF-2522|||S-Oxiracetam；(S)-ISF-2522|||S-Oxiracetam
(S)-Oxiracetam is a positive allosteric the AMPA receptorsmodulator.
价 格：￥电议型 号：T1128L产 地：中国大陆
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T11285FIDAS-5；化合物FIDAS-5FIDAS-5
FIDAS-5, a potent and orally active methionine S-adenosyltransferase 2A (MAT2A) inhibitor with an IC50 of 2.1 μM, competitively inhibits S-adenosylmethionine (SAM) binding to MAT2A. It exhibits anticancer activities.
价 格：￥电议型 号：T11285产 地：中国大陆
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T11284FIDAS-3；化合物FIDAS-3FIDAS-3
FIDAS-3, a stilbene derivative and potent Wnt inhibitor with an IC50 of 4.9 μM for methionine S-adenosyltransferase 2A (MAT2A), exhibits anticancer activities by effectively competing with S-adenosylmethionine (SAM) for MAT2A binding.
价 格：￥电议型 号：T11284产 地：中国大陆
