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TN1599Eburicoic acid
Eburicoic acid exhibits anti-inflammatory and antioxidant activity thereby protecting the liver from CCl4-induced hepatic damage and can be used in studies about anti-liver cancer.
价 格：￥电议型 号：TN1599产 地：中国大陆
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T11599Ibiglustat (L-Malic acid)
Ibiglustat (L-Malic acid) is a selective, brain-penetrant, and allosteric inhibitor of glucosylceramide synthase. Ibiglustat (L-Malic acid) can be used in studies about PD Parkinson’s disease, SRT in Fabry’s and Gaucher’s.
价 格：￥电议型 号：T11599产 地：中国大陆
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T2103Ispinesib伊匹尼塞；伊斯平斯；CK0238273；SB-715992
Ispinesib, a selective, effectvie and reversible inhibitor of kinesin spindle protein (KSP), is derived from quinazolinone, with antineoplastic properties.
价 格：￥电议型 号：T2103产 地：中国大陆
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T0860LMefloquine氟甲喹羟哌啶；Ro215998；Ro-215998；Ro 215998；WR 142490；Lariam
Mefloquine, a quinoline antimalarial agent, is an anti-SARS-CoV-2 entry inhibitor. Mefloquine is also a K+ channel (KvQT1/minK) antagonist with an IC50 of ~1 μM. Mefloquine can be used for malaria, systemic lupus erythematosus, and cancer research.
价 格：￥电议型 号：T0860L产 地：中国大陆
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T11599Ibiglustat L-Malic acidIbiglustat L-Malic acid,Venglustat (L-Malic acid),SAR402671 (L-Malic acid)
Ibiglustat L-Malic acid (Venglustat L-Malic acid), a potential therapy for PD Parkinson’s disease.
价 格：￥电议型 号：T11599产 地：美洲
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T2103IspinesibIspinesib,SB-715992,CK0238273
Ispinesib, a selective, effectvie and reversible inhibitor of kinesin spindle protein (KSP), is derived from quinazolinone, with antineoplastic properties.
价 格：￥电议型 号：T2103产 地：美洲
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T81599Orenetide；化合物 OrenetideOrenetide
Orenetide is an innovative peptide-based pharmaceutical designed to rejuvenate sexual desire and associated functions in women suffering from hypoactive sexual desire disorder (HSDD) [1].
价 格：￥电议型 号：T81599产 地：中国大陆
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T71599AqB007；化合物 AqB007AqB007
AqB007 is a selective blocker of the Aquaporin-1 ion channel conductance, thereby slowing cancer cell migration.
价 格：￥电议型 号：T71599产 地：中国大陆
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T61599XT2；化合物 XT2XT2
XT2 is a highly potent, orally active, and selective inhibitor of NF-κB-inducing kinase (NIK), exhibiting an IC50 of 9.1 nM. It effectively suppresses the upregulation of ALT, a vital biomarker for acute liver injury, induced by CCl4. Additionally, XT2 significantly decreases immune cell infiltration into the damaged liver tissue. As a result, XT2 holds immense potential in liver inflammatory disease research [1].
价 格：￥电议型 号：T61599产 地：中国大陆
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T39091Spectinamide 1599；Spectinamide 1599Spectinamide 1599
Spectinamide-1599 is a combination partner for anti-tuberculosis therapy.
价 格：￥电议型 号：T39091产 地：中国大陆
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T31599Echinosporin；化合物 T31599XK-213|||XK213|||XK 213；XK-213|||XK213|||XK 213
Echinosporin is a biochemical.
价 格：￥电议型 号：T31599产 地：中国大陆
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T2103Ispinesib；伊斯平斯CK0238273|||SB-715992；伊匹尼塞|||伊斯平斯|||CK0238273|||SB-715992
Ispinesib (SB-715992), a selective, effectvie and reversible inhibitor of kinesin spindle protein (KSP), is derived from quinazolinone, with antineoplastic properties.
价 格：￥电议型 号：T2103产 地：中国大陆
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T15999Mal-PEG6-acid；化合物 T15999Mal-PEG6-acid
Mal-PEG6-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15999产 地：中国大陆
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T15998Mal-PEG5-PFP ester；化合物 T15998Mal-PEG5-PFP ester
Mal-PEG5-PFP ester is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15998产 地：中国大陆
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T15997Mal-PEG5-NHS ester；化合物 T15997Mal-PEG5-NHS ester
Mal-PEG5-NHS ester, an alkyl/ether and PEG-based PROTAC linker, is utilized for the synthesis of PROTACs.
价 格：￥电议型 号：T15997产 地：中国大陆
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T15996Mal-PEG5-acid；化合物 T15996Mal-PEG5-acid
Mal-PEG5-acid is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15996产 地：中国大陆
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T15995Mal-PEG4-Val-Cit-PAB-PNP；化合物 T15995Mal-PEG4-Val-Cit-PAB-PNP|||Mal PEG4 Val Cit PAB PNP|||Mal-PEG-4-V
Mal-PEG4-Val-Cit-PAB-PNP is a cleavable 4-unit polyethylene glycol (PEG) linker employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15995产 地：中国大陆
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T15994Mal-PEG4-Val-Cit-PAB-OH；化合物 T15994Mal-PEG4-Val-Cit-PAB-OH
Mal-PEG4-Val-Cit-PAB-OH, a cleavable 4-unit PEG ADC linker, is employed in the synthesis of antibody-drug conjugates (ADCs)[1].
价 格：￥电议型 号：T15994产 地：中国大陆
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T15993Mal-PEG4-PFP ester；化合物 T15993Mal-PEG4-PFP ester
Mal-PEG4-PFP ester is a non-cleavable antibody-drug conjugate (ADC) linker that incorporates a Maleimide moiety, a 4-unit Polyethylene Glycol (PEG) backbone, and a Pentafluorophenyl (PFP) ester.
价 格：￥电议型 号：T15993产 地：中国大陆
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T15992Mal-PEG4-OH；化合物 T15992Mal-PEG4-OH
Mal-PEG4-OH is a PEG-based linker for PROTACs which joins two essential ligands, crucial for forming PROTAC molecules. This linker enables selective protein degradation by leveraging the ubiquitin-proteasome system within cells.
价 格：￥电议型 号：T15992产 地：中国大陆
