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T11920LysRs-IN-2；化合物 T11920LysRs-IN-2
LysRs-IN-2 is a lysyl-tRNA synthetase (KRS) inhibitor with IC50s of 0.13 μM and 0.015 μM for Cryptosporidium parvum lysyl-tRNA synthetase (CpKRS) and Plasmodium falciparum lysyl-tRNA synthetase (PfKRS), respectively.
价 格：￥电议型 号：T11920产 地：中国大陆
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T11919LysRs-IN-1；化合物LysRs-IN-19-carboxymethylguanine；9-carboxymethylguanine
LysRs-IN-1 is an inhibitor of Lysyl-tRNA synthetase (LysRs).
价 格：￥电议型 号：T11919产 地：中国大陆
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T11917Lys-SMCC-DM1；化合物Lys-SMCC-DM1Lys-Nε-MCC-DM1；Lys-Nε-MCC-DM1
DM1 is a tubulin inhibitor. Lys-SMCC-DM1 (Lys-Nε-MCC-DM1) is the active metabolite of DM1.
价 格：￥电议型 号：T11917产 地：中国大陆
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T11902LY 344864 S-enantiomer；化合物 T11902LY 344864 S-enantiomer
LY 344864 S-enantiomer, the S-enantiomer of LY344864, serves as a 5-HT1F receptor agonist.
价 格：￥电议型 号：T11902产 地：中国大陆
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T11888LtaS-IN-1；化合物LtaS-IN-1LtaS-IN-1
LtaS-IN-1 is an effective inhibitor of Lipoteichoic acid synthesis in multidrug-resistant (MDR) E. faecium and by altering the cell wall morphology. LtaS-IN-1 is against Enterococcus spp 28 strains with varying MIC values ranging from 0.5 μg/mL to 64 μg/mL. LtaS-IN-1 inhibits strain E1630 and E1590 with MIC values of 0.5 μg/mL.
价 格：￥电议型 号：T11888产 地：中国大陆
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T11879LS-102；化合物 T11879LS-102
LS-102, a selective E3 ubiquitin ligase synoviolin (Syvn1) inhibitor, effectively inhibits the autoubiquitination of synoviolin, exhibiting an IC50 value of 35 μM. This compound shows promise for the treatment of rheumatoid arthritis.
价 格：￥电议型 号：T11879产 地：中国大陆
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T11832Ledipasvir D-tartrate；雷迪帕韦 D-酒石酸GS-5885 D-tartrate；GS-5885 D-tartrate|||雷迪帕韦 D-酒石酸
Ledipasvir D-tartrate with EC50 values of 34 pM against GT1a and 4 pM against GT1b replicon. is an inhibitor of the hepatitis C virus NS5A.
价 格：￥电议型 号：T11832产 地：中国大陆
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T1183Retinol视黄醇all-trans-Retinol|||视黄醇|||Vitamin A|||Vitamin A1|||Alphalin
Retinol (Vitamin A) is a natural vitamin that is fat soluble. Retinol plays an important role in the metabolic functions of the retina, growth and differentiation of epithelial tissues, bone growth, reproduction and immune response.
价 格：￥电议型 号：T1183产 地：中国大陆
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T11824LLLanraplenib；化合物LanraplenibGS-9876；GS-9876
Lanraplenib (GS-9876) is a highly selective and orally active SYK inhibitor (IC50=9.5 nM) in development for the treatment of inflammatory diseases. Lanraplenib inhibits SYK activity in platelets via the glycoprotein VI (GPVI) receptor without prolonging bleeding time (BT) in monkeys or humans.
价 格：￥电议型 号：T11824LL产 地：中国大陆
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T11824LLanraplenib monosuccinate；化合物 T11824LGS-9876 monosuccinate；GS-9876 monosuccinate
Lanraplenib monosuccinate inhibits SYK activity in platelets via the glycoprotein VI (GPVI) receptor without prolonging bleeding time (BT) in monkeys or humans. Lanraplenib monosuccinate is a highly selective and orally active SYK inhibitor (IC50=9.5 nM) in development for the treatment of inflammatory diseases.
价 格：￥电议型 号：T11824L产 地：中国大陆
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T11824Lanraplenib succinate化合物 T11824GS-9876 succinate
Lanraplenib succinate inhibits SYK activity in platelets via the glycoprotein VI (GPVI) receptor without prolonging bleeding time (BT) in monkeys or humans. Lanraplenib succinate is a highly selective and orally active SYK inhibitor (IC50=9.5 nM) in development for the treatment of inflammatory diseases.
价 格：￥电议型 号：T11824产 地：中国大陆
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T11740Delcasertib；化合物DelcasertibKAI-9803|||BMS-875944；KAI-9803|||BMS-875944
Delcasertib (KAI-9803) is a potent and selective inhibitor of δ-protein kinase C (δPKC).
价 格：￥电议型 号：T11740产 地：中国大陆
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T11675Irbesartan-d4；厄贝沙坦 D4SR-47436 D4|||BMS-186295 D4；厄贝沙坦 D4|||SR-47436 D4|||BMS-186295 D4
Irbesartan D4, a deuterium-labeled variant of Irbesartan, is a highly potent and specific antagonist of the angiotensin II type 1 (AT1) receptor.
价 格：￥电议型 号：T11675产 地：中国大陆
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T11662LINT-777；化合物INT-777S-EMCA；S-EMCA
INT-777 (S-EMCA) is a potent TGR5 agonist with an EC50 of 0.82 μM. INT-777 (S-EMCA) inhibits NLRP5-ASC inflammasome-mediated neuroinflammation via the TGR3/cAMP/PKA signaling pathway after subarachnoid hemorrhage in rats.
价 格：￥电议型 号：T11662L产 地：中国大陆
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T11662INT-777 R-enantiomer；化合物 T11662S-EMCA R enantiomer；S-EMCA R enantiomer
INT-777 is the R-enantiomer of INT-777, less potent than INT-777,EC50 of 4.79 μM for TGR5.
价 格：￥电议型 号：T11662产 地：中国大陆
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T11628IACS-8968 S-enantiomer；化合物 T11628IDO/TDO Inhibitor (S-enantiomer)；IDO/TDO Inhibitor (S-enantiomer)
IACS-8968 S-enantiomer is the S-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
价 格：￥电议型 号：T11628产 地：中国大陆
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T11627IACS-8968 R-enantiomer；化合物 T11627IDO/TDO Inhibitor (R-enantiomer)；IDO/TDO Inhibitor (R-enantiomer)
IACS-8968 R-enantiomer is the R-enantiomer of IACS-8968. IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
价 格：￥电议型 号：T11627产 地：中国大陆
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T11626IACS-8968；化合物 T11626IDO/TDO Inhibitor；IDO/TDO Inhibitor
IACS-8968 is a dual IDO and TDO inhibitor (pIC50s: 6.43 for IDO and <5 for TDO).
价 格：￥电议型 号：T11626产 地：中国大陆
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T11616IDO-IN-13；化合物IDO-IN-13GS-4361；GS-4361
IDO-IN-13 (GS-4361) is a potent indoleamine 2,3-dioxygenase 1 (IDO1) inhibitor (EC50: 17 nM).
价 格：￥电议型 号：T11616产 地：中国大陆
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T11610Idelalisib D5；化合物 T11610CAL-101 D5|||GS-1101 D5；CAL-101 D5|||GS-1101 D5
Idelalisib D5, a version of Idelalisib marked with deuterium, is an orally bioavailable and highly selective inhibitor of p110δ.
价 格：￥电议型 号：T11610产 地：中国大陆
