Structure | Cat No. | Product Name | CAS No. | Product Description |
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V25436 | Methylsilanol PCA | 105883-41-8 | Methylsilanol PCA is a novel and potent bioactive compound |
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V12057 | Methylstat | 1310877-95-2 | Methylstat is a novel and potent inhibitor of the Jumonji C domain-containing histone trimethyl demethylases (JHDMs)with anti-proliferative activity and low cytotoxicity. |
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V25437 | Methyltetrazine-acid | 1380500-88-8 | Methyltetrazine-acid is a PROTAC (PROteolysis TArgeting Chimera) linker of the alkyl chain class, may be utilized to prepare PROTAC protein degraders. |
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V25438 | Methyltetrazine-amine HCl salt | 1345955-28-3 | Methyltetrazine-Amine is a tetrazine compound that may be utilized to prepare site-specific bifunctional bioconjugates. |
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V25439 | Methyltetrazine-DBCO | 1802238-48-7 | Methyltetrazine-DBCO is a non-cleavable (non-degradable) ADC linker that may be utilized to prepare antibody-conjugated active molecules (ADC). |
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V25440 | Methyltetrazine-NHS ester | 1644644-96-1 | Methyltetrazine-Ph-NHS ester is a PROTAC (PROteolysis TArgeting Chimera) linker of the alkyl/ether class, may be utilized to prepare PROTAC protein degraders. |
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V25441 | Methyltetrazine-PEG4-amine HCl salt | 1802908-05-9 | Methyltetrazine-PEG4-amine is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders. |
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V25442 | Methyltetrazine-PEG4-azide | 1802908-04-8 | Methyltetrazine-Ph-PEG4-azide is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders. |
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V25443 | Methyltetrazine-PEG4-maleimide | 1802908-02-6 | Methyltetrazine-PEG4-maleimide is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders. |
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V25444 | Methyltetrazine-PEG5-alkyne | 1802907-97-6 | Methyltetrazine-PEG5-alkyne is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders. |
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V25445 | Methyltetrazine-PEG5-NHS ester | 1802907-92-1 | Methyltetrazine-PEG5-NHS ester is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders. |
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V25446 | Methyltetrazine-PEG8-acid | 2183440-33-5 | Methyltetrazine-PEG8-acid is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders. |
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V25447 | Methyltetrazine-PEG8-NHS ester | 2183440-34-6 | Methyltetrazine-PEG8-NHS ester is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders. |
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V25448 | Methyltetrazine-propylamine HCl salt | 1802978-47-7 | Methyltetrazine-propylamine is a PROTAC (PROteolysis TArgeting Chimera) linker of the alkyl chain class, may be utilized to prepare PROTAC protein degraders. |
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V7162 | Mexrenone | 41020-65-9 | Mexrenone is a novel and potent steroidal antimineralocorticoid of the spirolactone group |
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V25483 | MF 13 | 38232-20-1 | MF 13 is a novel and potent tumor apoptosis acivity |
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V25484 | Mf 268 | 154619-51-9 | Mf 268 is a novel and potent carbamate-type inhibitor |
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V25485 | MF 961 | 138372-62-0 | MF 961 is a novel and potent quinolone antimicrobial agent |
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V9992 | MF-438 | 921605-87-0 | MF-438 is a potent and orally bioavailable inhibitor of staroyl-CoA desaturase 1 (SCD1) with IC50 of 2.3 nM for rSCD1. |
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V21418 | MF-592 | 1064195-48-7 | MF-592 is a novel and potent antagonists of the EP4 receptor |