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T17913(S,R,S)-AHPC-PEG2-N3化合物T17913VHL Ligand-Linker Conjugates 6|||VH032-PEG2-N3|||E3 ligase Ligand-Linke
(S,R,S)-AHPC-PEG2-N3 (VHL Ligand-Linker Conjugates 6) is a synthesized E3 ligase ligand-linker conjugate containing a (S,R,S)-AHPC based VHL ligand and 2 unit PEG linker.
价 格：￥电议型 号：T17913产 地：中国大陆
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T17912(S,R,S)-AHPC-(C3-?PEG)?2-?C6-?Cl；化合物 T17912VHL Ligand-Linker Conjugates 11|||E3 ligase Ligand-Linker
(S,R,S)-AHPC-(C3- PEG) 2- C6- Cl is a small molecule HaloPROTAC that incorporates the (S,R,S)-AHPC based VHL ligand and 2-unit PEG linker. (S,R,S)-AHPC-(C3- PEG) 2- C6- Cl is capable of inducing the degradation of GFP-HaloTag7 in cell-based assays[1].
价 格：￥电议型 号：T17912产 地：中国大陆
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T17911(S,R,S)-AHPC-C6-PEG3-C4-Cl；化合物 T17911VH032-C6-PEG3-C4-Cl|||VHL Ligand-Linker Conjugates 12|||E3 liga
(S,R,S)-AHPC-C6-PEG3-C4-Cl is a small molecule HaloPROTAC that incorporates the (S,R,S)-AHPC based VHL ligand and 3-unit PEG linker. (S,R,S)-AHPC-C6-PEG3-C4-Cl is capable of inducing the degradation of GFP-HaloTag7 in cell-based assays[1].
价 格：￥电议型 号：T17911产 地：中国大陆
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T17910(S,R,S)-AHPC-PEG2-C4-Cl；化合物 T17910E3 ligase Ligand-Linker Conjugates 10|||VHL Ligand-Linker Conjugat
(S,R,S)-AHPC-PEG2-C4-Cl is a small molecule HaloPROTAC that incorporates the (S,R,S)-AHPC based VHL ligand and 2-unit PEG linker. (S,R,S)-AHPC-PEG2-C4-Cl is capable of inducing the degradation of GFP-HaloTag7 in cell-based assays[1].
价 格：￥电议型 号：T17910产 地：中国大陆
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T1791Ceritinib；色瑞替尼LDK378；色瑞替尼|||LDK378
Ceritinib (LDK378) is a specific ALK inhibitor (IC50: 0.2 nM).
价 格：￥电议型 号：T1791产 地：中国大陆
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T17891cIAP1 Ligand-Linker Conjugates 2；化合物 T17891E3 ligase Ligand-Linker Conjugates 37；E3 ligase Ligand-Li
cIAP1 Ligand-Linker Conjugates 2 is a chemical compound that combines an IAP ligand for the E3 ubiquitin ligase with a PROTAC linker. This compound is particularly useful in the design of SNIPERs [1].
价 格：￥电议型 号：T17891产 地：中国大陆
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T1780LParecoxib sodium帕瑞昔布钠SC 69124A|||SC-69124A|||帕瑞昔布钠|||SC69124A|||Dynastat
Parecoxib is a cyclooxygenase-2 inhibitor used for the short-term treatment of postoperative pain in adults. Parecoxib is a water-soluble and injectable prodrug of valdecoxib. Parecoxib is a COX2 selective inhibitor in the same category as celecoxib and rofecoxib. ketorolac has a much higher gastrointestinal toxicity profile compared to most other nonsteroidal anti-inflammatory drugs including ibuprofen and Naprosyn.
价 格：￥电议型 号：T1780L产 地：中国大陆
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T1780Parecoxib；帕瑞昔布SC 69124|||Vorth-P|||Valus-P；SC 69124|||帕瑞昔布|||Vorth-P|||Valus-P
Parecoxib (SC 69124) is an effective and selective COX-2 inhibitor.
价 格：￥电议型 号：T1780产 地：中国大陆
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T17791DBCO-PEG3-NHS ester；DBCO-PEG3-NHS酯DBCO-PEG3-NHS ester
DBCO-PEG3-NHS ester is a degradable ADC linker that can be used to synthesize antibody-coupled active molecules.
价 格：￥电议型 号：T17791产 地：中国大陆
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T17691Boc-Val-Cit-OH；化合物Boc-Val-Cit-OHBoc-Val-Cit-OH
Boc-Val-Cit-OH is a cleavable ADC linker used in antibody-drug conjugates (ADCs) synthesis.
价 格：￥电议型 号：T17691产 地：中国大陆
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T1769Pardoprunox；帕多芦诺SLV-308|||DU-126891；帕多芦诺|||SLV-308|||DU-126891
Pardoprunox (SLV-308) is a partial dopamine D2 agonist and noradrenergic agonist with serotonin 5-HT1A agonist properties. Pardoprunox has been used in trials studying the treatment of Early Stage Parkinson´s Disease and Advanced Stage Parkinson´s Disease.
价 格：￥电议型 号：T1769产 地：中国大陆
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T17591Biotin-PEG6-Boc；生物素-六聚乙二醇-丙酸叔丁酯Biotin-PEG6-t-butyl ester；生物素-六聚乙二醇-丙酸叔丁酯|||Biotin-PEG6-t-butyl ester
Biotin-PEG6-Boc (Biotin-PEG6-t-butyl ester) is a PEG-based PROTAC linker that can be used in PROTAC synthesis.
价 格：￥电议型 号：T17591产 地：中国大陆
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T17491Azido-PEG16-NHS ester；化合物 T17491Azido-PEG16-NHS ester
Azido-PEG16-NHS 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：T17491产 地：中国大陆
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T17391Amine-PEG-amine (MW 20000)；化合物 T17391Amine-PEG-amine (MW 20000)
Amine-PEG-amine (MW 20000) is a polyethylene glycol (PEG)-based linker compound utilized in the synthesis of PROTACs.
价 格：￥电议型 号：T17391产 地：中国大陆
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T17291ZK 216348；化合物 T17291(+)-ZK 216348；(+)-ZK 216348
ZK 216348 also binds to Progesterone and mineralocorticoid receptors (IC50s: 20.4 nM and 79.9 nM, respectively). ZK 216348 is a nonsteroidal selective glucocorticoid receptor agonist (IC50: 20.3 nM). ZK 216348 has an anti-inflammatory activity similar to Prednisolone.
价 格：￥电议型 号：T17291产 地：中国大陆
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T17262XE 991 dihydrochloride；化合物XE 991 dihydrochlorideXE 991 dihydrochloride
XE 991 dihydrochloride is a Kv7 (KCNQ) channel blocker. XE 991 dihydrochloride potently inhibits Kv7.1 (KCNQ1), Kv7.2 (KCNQ2), Kv7.2 + Kv7.3 (KCNQ3) channel, and M-current (IC50s: 0.75 μM, 0.71 μM, 0.6 μM, and 0.98 μM, respectively).
价 格：￥电议型 号：T17262产 地：中国大陆
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T17191Bunaprolast；布那司特U66858；U66858
Bunaprolast (U66858) is a novel and potent leukotriene B4 (LTB4) inhibitor.Bunaprolast exhibits oxidative degradation activity and inhibits lipoxygenase and TXB2 release.
价 格：￥电议型 号：T17191产 地：中国大陆
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T17106TMC310911；化合物 T17106TMC310911
TMC310911 is an effective and orally active HIV type-1 protease inhibitor (EC50: ranged from 2.2 nM to 14.2 nM for wild-type HIV-1). TMC310911 has effective activity against a wide spectrum of recombinant HIV-1 isolates.
价 格：￥电议型 号：T17106产 地：中国大陆
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T17091Thrombin Inhibitor 2；化合物 T17091Thrombin Inhibitor 2
Thrombin Inhibitor 2 is a small molecule direct thrombin inhibitor. Thrombin Inhibitor 2 has antithrombotic activity.
价 格：￥电议型 号：T17091产 地：中国大陆
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T17033Temanogrel；化合物TemanogrelAPD791；APD791
Temanogrel (APD791) is a highly selective antagonist of the 5-HT2A receptor (Ki: 4.9 nM).
价 格：￥电议型 号：T17033产 地：中国大陆
