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N-Biotinyl-12-aminododecanoic acid is a compound formed by linking biotin and 12-aminododecanoic acid through an amide bond. N-Biotinyl-12-aminododecanoic acid is used as a biotinylation reagent to test the ligation activity of SimL.

16-Phenoxy tetranor Prostaglandin F2α cyclopropyl methyl amide (16-Phenoxy tetranor PGF2α cyclopropyl methyl amide) is the amidated form of 16-Phenoxy tetranor prostaglandin F2α (HY-139063).

Zidovudine Glucuronide-¹³C₆ (3'-Azido-3'-deoxythymidine β-D-glucuronide-¹³C₆) is ¹³C labeled Zidovudine O-β-D-glucuronide. Zidovudine O-β-D-glucuronide (3'-Azido-3'-deoxythymidine β-D-glucuronide) sodium is the major metabolite of Zidovudine. Zidovudine is a nucleoside reverse transcriptase inhibitor (NRTI), widely used to treat HIV infection.

8-MA-cAMP (8-Methylamino-cAMP) is a cyclic AMP analog that acts as a site-selective PKA agonist with similar affinity for the B site of type I and type II protein kinase A. 8-MA-cAMP is used in conjunction with priming analogs that show site A preference, such as 8-piperidinyl cAMP, to achieve selective stimulation of type I.

Phenyl-1-thio-β-D-glucopyranoside can be used in glycobiology research.

Reduced Haloperidol-d₄ is the deuterium labeled Reduced Haloperidol.

Terbutalone is a derivative of Terbutaline (HY-B0802A). Terbutaline is an orally active β₂-adrenergic receptor agonist and an active metabolite of Bambuterol (HY-17501). Terbutaline can be used in asthma symptom research.

Terbinafine impurity 13 is an impurity of Terbinafine.

Nicotinamide 1,N6-ethenoadenine dinucleotide (ε-NAD) sodium, a fluorescent analogue of NAD, is able to serve as a substrate for the bacterial toxincatalyzed G-ADP ribosylation of signal-transducing G-proteins. Nicotinamide 1,N6-ethenoadenine dinucleotide sodium can be used as a fluorescent substrate for the studies of the ADP ribosylation reaction.

P1,P2-Diuridine-5’-diphosphate (Up2U) is a symmetrical dinucleoside polyphosphate containing two pyrimidine base moieties. P1,P2-Diuridine-5’-diphosphate is also an activator of purinergic P2Y receptor.

Sp-GTPαS tetrasodium is a phosphonothioate analog of GTP (HY-113225). Sp-GTPαS tetrasodium is more metabolically stable than GTP.

Rp-GTPαS tetrasodium is a phosphorothioate analogue of Guanosine triphosphate (GTP) (HY-113225) that can activate calcium release and secretion in single rat peritoneal mast cells.

Sp-GDPαS trisodium is a regulator of GDP-binding proteins. Sp-GDPαS trisodium is metabolically more stable than GTP.

Rp-GDPαS (trisodium) is an isomer of the sulfur-containing nucleotide derivative GDP-α-S.

Sp-dUTPαS tetrasodium is an isomer of the sulfur-containing nucleotide dUTPαS.

Sp-dGDPαS is a regulator of GDP-binding proteins. Sp-dGDPαS is metabolically more stable than GTP.

Sp-dCTPαS is a regulator of CTP-binding proteins. Sp-dCTPαS is metabolically more stable than CTP.

Sp-dADPαS is a regulator of ADP-binding proteins. Sp-dADPαS is metabolically more stable than ATP.

Sp-cCMPS is a cCMP analog that activates the binding protein of cCMP.

Sp-cAMPS-AM is an analog of cAMP. Sp-cAMPS-AM acts as the inducer of PKA activation and CREB phosphorylation, through entrance into the cell and release of its parent polar structure Sp-cAMPS.