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Structure Cat No. Product Name CAS No. Product Description
( )-脱氢枞酸 V38509 (+)-Dehydroabietic acid 1231-75-0 (+)-Dehydroabietic acid is a diterpene.
(+)-CBI-CDPI1 V33334 (+)-CBI-CDPI1 128300-14-1 (+)-CBI-CDPI1 is an enhanced functional analogue of CC-1065, which is a DNA alkylating agent that has been used as a cytotoxic warhead in the synthesis of ADC (antibody drug conjugate).
(+)-CBI-CDPI2 V33333 (+)-CBI-CDPI2 128300-15-2 (+)-CBI-CDPI2 is a novel enhanced functional analogue of CC-1065, which is a DNA alkylator used as a cytotoxic warhead in ADC (antibody drug conjugate).
(+)-DHMEQ V31073 (+)-DHMEQ 287194-41-6 (+)-DHMEQ is an activator of the antioxidant transcription factor Nrf2.
(+)-Dihydrexidine hydrochloride V32557 (+)-Dihydrexidine hydrochloride 158704-02-0 (+)-Dihydrexidine HCl ((+)-DAR-0100 HCl) is a dopamine D1 receptor agonist (activator) with EC50 of 72±21 nM.
(+)-KCC2阻滞剂1 V38941 (+)-KCC2 blocker 1 1228439-71-1 (+)-KCC2 blocker 1 is a selective blocker of the K+-Cl- co-transporter KCC2 with IC50 of 0.4 μM.
(+)-PD 128907, 盐酸盐; V31016 (+)-PD 128907 hydrochloride 300576-59-4 (+)-PD 128907 HCl is a selective agonist of dopamine D2/D3 receptors.
(+)-SJ733 V32905 (+)-SJ733 1424799-20-1 (+)-SJ733 is an antimalarial agent and a Na+-ATPase PfATP4 inhibitor.
(+)-冰片 V30504 (+)-Borneol 464-43-7 (+)-Borneol is a novel and potent bicyclic monoterpene
(+)-布雷他汀 (R-Blebbistatin) V38758 (+)-Blebbistatin (R-Blebbistatin) 1177356-70-5 Blebbistatin is a specific inhibitor of myosin II ATPase.
(+)-异蒲勒醇 V38704 (+)-Isopulegol 104870-56-6 (+)-Isopulegol is a terpenoid found in the Canadian mint tree and has a stimulating effect on adults of S.
(+)-异薄荷酮 V40524 (+)-Isomenthone 1196-31-2 (+)-Isomenthone is an isomenthone extracted from Ziziphora clinopodioides Lam.
(+)-生物素-PEG1-OH V39438 (+)-Biotin-PEG10-OH (+)-Biotin-PEG10-OH is a novel and potent PROTAC linker
(+)-生物素-PEG12-OH V39278 (+)-Biotin-PEG12-OH (+)-Biotin-PEG12-OH is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders.
(+)-生物素-PEG2-酰肼 V39537 (+)-Biotin-PEG2-hydrazide (+)-Biotin-PEG2-hydrazide is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders.
(+)-生物素-PEG6-酰肼 V39363 (+)-Biotin-PEG6-hydrazide (+)-Biotin-PEG6-hydrazide is a PROTAC (PROteolysis TArgeting Chimera) linker of the Polyethylene glycol (PEG) category, may be utilized to prepare PROTAC protein degraders.
(+)-生物素ONP V39349 (+)-Biotin-ONP 33755-53-2 (+)-Biotin-ONP is a PROTAC (PROteolysis TArgeting Chimera) linker of the alkyl chain class, may be utilized to prepare PROTAC protein degraders.
(+)-生物素SLC V39436 (+)-Biotin-SLC 1864003-57-5 (+)-Biotin-SLC is a PROTAC (PROteolysis TArgeting Chimera) linker of the alkyl chain category, may be utilized to prepare PROTAC protein degraders.
(+)-酮康唑 V32920 (+)-Ketoconazole 142128-59-4 (+)-Ketoconazole ((+)-R 41400) is an imidazole antifungal compound/agent and CYP3A4 inhibitor.
(-)-(S)-B-973B V31453 (-)-(S)-B-973B 2244989-34-0 (-)-(S)-B-973B is a potent positive allosteric modulator (PAM) of α7 nAChR and may be utilized in pain relief research.
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