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Val-cit-PAB-OH / 10 g

Synonym: Val-Cit-PAB; L-valyl-N5-carbamoyl-N-[4-(hydroxymethyl)phenyl]-L-omithinamide; (S)-2-((S)-2-amino-3-methylbutanamido)-N-(4-(hydroxymethyl)phenyl)-5-ureidopentanamide
Molecular Formula: C18H29N5O4
Molecular Weight: 379.50
SKU: MND-190046
CAS Number: 159857-79-1
MDL number: MFCD22381209
Packing size: 10 g  



Safety Information


Hazard Statements

H302
H315
H319
H335

Precautionary Statements

P280
P264
P270
P501
P305 + P351 + P338
P261
P271
P405
P302 + P352
P362 + P364
P403 + P233
P304 + P340
P330
P321
P264 + P265
P319
P332 + P317
P337 + P317
P301 + P317

Pictograms



Properties

Signal WordWarning

 Product Description

Val-cit-PAB-OH is a synthetic prodrug designed for targeted delivery of cytotoxic agents in cancer therapy. It consists of valine, citrulline, and p-aminobenzoic acid linked together, forming a molecule that can be selectively taken up by certain types of cancer cells. Upon entering these cells, Val-cit-PAB-OH undergoes metabolic activation to release the active cytotoxic component, which then targets and kills the cancer cells. This targeted approach aims to minimize damage to healthy tissues, potentially improving patient outcomes and reducing side effects associated with conventional chemotherapy.

 

Application

In clinical settings, Val-cit-PAB-OH is being explored as part of novel strategies in cancer treatment, particularly for solid tumors that overexpress specific transporters. Its use in combination therapies could enhance the efficacy of existing treatments by delivering higher concentrations of cytotoxic agents directly to tumor sites. Research into Val-cit-PAB-OH is ongoing, focusing on optimizing its formulation and delivery mechanisms to maximize its therapeutic potential.

 

 

Articles:

- Protease-Mediated Fragmentation of p-Amidobenzyl Ethers:  A New Strategy for the Activation of Anticancer Prodrugs

Publication Date: February 12, 2002

Brian E. Toki, Charles G. Cerveny, Alan F. Wahl, and Peter D. Senter

https://doi.org/10.1021/jo016187+

 

- Systematic Variation of Pyrrolobenzodiazepine (PBD)-Dimer Payload Physicochemical Properties Impacts Efficacy and Tolerability of the Corresponding Antibody–Drug Conjugates

Publication Date: July 31, 2020

Leanna R. Staben, Jinhua Chen, Josefa dela Cruz-Chuh, Geoff del Rosario, Mary Ann Go, Jun Guo, S. Cyrus Khojasteh, Katherine R. Kozak, Guangmin Li, Carl Ng, Gail D. Lewis Phillips, Thomas H. Pillow, Rebecca K. Rowntree, John Wai, BinQing Wei, Keyang Xu, Zijin Xu, Shang-Fan Yu, Donglu Zhang, and Peter S. Dragovich

https://doi.org/10.1021/acs.jmedchem.0c00691

 

- Targeting conserved N-glycosylation blocks SARS-CoV-2 variant infection in vitro

Publication Date: November 25, 2021

Hsiang-Chi Huang, Yun-Ju Lai, Chun-Che Liao, Feng-Yang Wang, Ke-Bin Huang, I-Jung Lee, Wen-Cheng Chou, Shih-Han Wang, Ling-Hui Wang, Jung-Mao Hsu, Cheng-Pu Sun, Chun-Tse Kuo, Jyun Wang, Tzu-Chun Hsiao, Po-Jiun Yang, Te-An Lee, Wilson Huang, Fu-An Li, Chen-Yang Shen, Yi-Ling Lin, Mi-Hua Tao, Chia-Wei Li

https://doi.org/10.1016/j.ebiom.2021.103712