Date published: 2025-10-15

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DBP Inhibitors

DBP inhibitors, belonging to a significant chemical class, are compounds that demonstrate a distinctive ability to interact with and modulate the function of di-n-butyl phthalate (DBP), a common industrial chemical and plasticizer. These inhibitors are characterized by their specific molecular structures that enable them to engage in targeted interactions with DBP molecules, thereby disrupting or altering their usual activities. The design and development of DBP inhibitors involve a meticulous understanding of the physicochemical properties of both the inhibitors and the target DBP compound. The intricate molecular interactions between DBP inhibitors and DBP itself are the cornerstone of their mechanism of action. These interactions often involve non-covalent bonding forces such as hydrogen bonding, van der Waals interactions, and hydrophobic interactions. Through these binding forces, DBP inhibitors effectively compete for binding sites on DBP molecules, resulting in a reduced or modified capacity of DBP to engage in its usual biochemical or physiological processes. Furthermore, DBP inhibitors hold promise in various applications due to their potential to modulate DBP's behavior, which is of significance in industrial and environmental contexts. The exploration of DBP inhibitors provides valuable insights into the complex interplay between chemical compounds and their molecular targets. As the field progresses, these inhibitors may contribute to the development of innovative strategies for managing and controlling DBP-related processes. In conclusion, DBP inhibitors represent a distinct chemical class that encompasses compounds capable of interacting with and influencing the function of di-n-butyl phthalate. The intricate molecular interactions between these inhibitors and DBP highlight the complexity and potential of this chemical class. The ongoing research and refinement of DBP inhibitors offer a promising avenue for applications in various domains, drawing upon the intimate knowledge of molecular interactions and structure-activity relationships.
Product NameCAS #Catalog #QUANTITYPriceCitationsRATING

Teneligliptin

760937-92-6 (free base)sc-475074
25 mg
$260.00
1
(0)

Teneligliptin inhibits DBP by competitively binding to its active site, obstructing the cleavage of dipeptides. This inhibition prolongs the action of incretin hormones, leading to enhanced insulin secretion and improved glucose utilization in diabetic conditions.

Vildagliptin

274901-16-5sc-208485
10 mg
$173.00
4
(1)

Vildagliptin inhibits DBP activity by competitively blocking its active site, hindering the cleavage of dipeptides. This inhibition results in prolonged action of incretin hormones, leading to enhanced insulin secretion and improved glucose homeostasis.

Sitagliptin

486460-32-6sc-482298
sc-482298A
sc-482298B
25 mg
100 mg
1 g
$209.00
$464.00
$719.00
10
(0)

Sitagliptin inhibits DBP by competitively binding to its active site, preventing the enzymatic cleavage of dipeptides. This inhibition leads to reduced breakdown of incretin hormones, ultimately resulting in increased insulin secretion and improved glycemic control.

Saxagliptin

361442-04-8sc-473161
1 mg
$360.00
(0)

Saxagliptin inhibits DBP by occupying its active site and obstructing substrate binding, thereby impeding the hydrolysis of dipeptides. This inhibition leads to elevated levels of intact incretin hormones, resulting in enhanced insulin secretion and improved glycemic control.

Trelagliptin

865759-25-7sc-507285
5 mg
$405.00
(0)

Trelagliptin inhibits DBP by binding to its active site, preventing the enzymatic hydrolysis of dipeptides. By interfering with DBP function, trelagliptin maintains elevated levels of circulating incretin hormones, leading to improved glucose-dependent insulin secretion and glycemic control.

Linagliptin

668270-12-0sc-364721
sc-364721A
5 mg
10 mg
$255.00
$418.00
2
(0)

Linagliptin inhibits DBP by forming a stable complex with the enzyme, blocking its catalytic activity. By directly interfering with DBP's function, linagliptin effectively suppresses the cleavage of dipeptides, thereby prolonging the action of incretin hormones and enhancing glucose-dependent insulin secretion.

Anagliptin

739366-20-2sc-507278
5 mg
$280.00
(0)

Alogliptin inhibits DBP by binding to its active site, preventing the enzyme from cleaving dipeptides. By competitively inhibiting DBP, alogliptin maintains higher levels of circulating incretin hormones, leading to increased insulin secretion and improved glucose metabolism.

Gemigliptin tartrate

1374639-74-3sc-507281
10 mg
$165.00
(0)

Gemigliptin inhibits DBP activity by forming a stable complex with the enzyme's active site, thereby preventing the hydrolysis of dipeptides. By blocking DBP function, gemigliptin maintains higher levels of circulating incretin hormones, promoting insulin secretion and glucose control.

Omarigliptin

1226781-44-7sc-507282
5 mg
$330.00
(0)

Omarigliptin inhibits DBP by competitively binding to its catalytic site, interfering with the cleavage of dipeptides. This inhibition results in elevated levels of intact incretin hormones, enhancing insulin secretion and improving glycemic regulation in diabetic individuals.

Evogliptin

1222102-29-5sc-507284
5 mg
$1060.00
(0)

Evogliptin inhibits DBP by forming a stable complex with the enzyme's active site, thereby preventing the cleavage of dipeptides. This inhibition leads to elevated levels of intact incretin hormones, promoting glucose-dependent insulin secretion and glycemic control in diabetic patients.