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DMG-PEG3400-CHO is a conjugate composed of dimyristic glycerol (DMG), a PEG chain, and a terminal aldehyde group (-CHO). DMG-PEG3400-CHO combines the membrane compatibility of phospholipids with the flexibility of hydroxyl modification, making it suitable for research in biomaterial construction and drug delivery.

DMG-PEG5000-CHO is a conjugate composed of dimyristic glycerol (DMG), a PEG chain, and a terminal aldehyde group (-CHO). DMG-PEG5000-CHO combines the membrane compatibility of phospholipids with the flexibility of hydroxyl modification, making it suitable for research in biomaterial construction and drug delivery.

DMG-PEG10000-CHO is a conjugate composed of dimyristic glycerol (DMG), a PEG chain, and a terminal aldehyde group (-CHO). DMG-PEG10000-CHO combines the membrane compatibility of phospholipids with the flexibility of hydroxyl modification, making it suitable for research in biomaterial construction and drug delivery.

L-Thyroxine-¹³C₉,¹⁵N is the ¹³C₆ ans ¹⁵N labeled L-Thyroxine (HY-18341).

Furanopetasin is an eremophilane-type sesquiterpene ester found in Petasites hybridus.

Duartin is an isoflavan that exists in the heartwood of Dalbergia odorifera T. Chen, Machaerium opacum, and Machaerium villosum Vog. Duartin shows no obvious inhibitory effect on prostaglandin biosynthesis, fails to alleviate rat paw edema induced by carrageenan, dextran, or histamine, and cannot inhibit carrageenan-induced pleurisy in rats, reduce exudate volume, or suppress leukocyte migration.

Bis-Mal-Suc-PEG10-bis (triAla)-Exatecan (CPT-113) is a cytotoxic payload/linker conjugate that forms antibody-drug conjugates (ADCs) with bispecific EGFR/Muc1 antibodies. Bis-Mal-Suc-PEG10-bis (triAla)-Exatecan is applicable for ADC synthesis.

JD128 (Compound 22) is a CDK4/6 inhibitor.

Exatecan-(D-2,4-DHB)-NH2-AA (bPEG8)-Mal is a linker-payload conjugate. Exatecan-(D-2,4-DHB)-NH2-AA (bPEG8)-Mal contains the linker D-2,4-DHB-NH2-AA(bPEG8)-Mal (HY-183595) and the cytotoxic agent Exatecan (HY-13631), a potent DNA topoisomerase I inhibitor. Exatecan-(D-2,4-DHB)-NH2-AA (bPEG8)-Mal can be utilized for the development of antibody-drug conjugates (ADCs).

GR-25 is an orally active, selective Hsp90p inhibitor.

M4K2009-CH2-piperidine (Compound 38) is a conjugate of an ALK ligand and a linker, which can be used for the synthesis of PROTACs, such as M4K3233 (HY-183717).

M4K2163-CH2-piperidine (Compound 42) is a conjugate of an ALK ligand and a linker, which can be used for the synthesis of PROTACs, such as M4K2163 (HY-183720).

4E1RCat 17d is a derivative of the ATG5 inhibitor lead compound T1742 (HY-183807). 4E1RCat 17d shows no activity against the interactions of ATG5-ATG16L1 and ATG5-TECAIR. 4E1RCat 17d induces Autophagy inhibition.

ATG5 PPI-IN-1 is a ATG5 protein-protein interaction inhibitor, with an IC₅₀ of 27.43 μM for the ATG5-ATG16L1 interaction and an IC₅₀ of 14.88 μM for the ATG5-TECAIR interaction.

4E1RCat 27d has a core structure of (E)-3-(2-furanylmethylene)-2-pyrrolidone. 4E1RCat 27d is an analog of 4E1rcat (HY-14427).

Chlorophyllide A is a tetrapyrrole metabolite late in the biosynthesis of chlorophylls and bacteriochlorophylls. Chlorophyllide A can be used as a photosensitizer for the research of photodynamic therapy-related research.

Dopamine D3 receptor agonist-2 is a selective dopamine D3 receptor partial agonist with a K_i of 0.268 nM. Dopamine D3 receptor agonist-2 exhibits 29-fold selectivity over dopamine D2 receptor (K_i= 7.67nM).

ATG5 PPI-IN-5 is a Autophagy-Related ATG5 protein-protein interaction inhibitor and autophagy inhibitor. The IC₅₀ values of ATG5 PPI-IN-5 for the interactions of ATG5-ATG16L1 and ATG5-TECAIR are >33 μM.

ATG5/TECAIR-IN-3 is a ATG5 inhibitor with autophagy inhibitory activity. ATG5/TECAIR-IN-3 selectively inhibits the ATG5-TECAIR interaction (IC₅₀=31.24 μM) and shows no activity against the ATG5-ATG16L1 interaction.

Autophagy-IN-10 is an Autophagy inhibitor and an inhibitor of ATG5 interaction with other proteins, with an IC₅₀ value of 2.29 μM against ATG5-ATG16L1 and an IC₅₀ value of 3.68 μM against ATG5-TECAIR.