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VH032-cyclopropane-F
[CAS# 2306193-99-5]

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Identification
Classification Organic raw materials >> Heterocyclic compound >> Pyrroles
Name VH032-cyclopropane-F
Synonyms N-[(1-Fluorocyclopropyl)carbonyl]-3-methyl-L-valyl-(4R)-4-hydroxy-N-[2-hydroxy-4-(4-methyl-1,3-thiazol-5-yl)benzyl]-L-prolinamide; (2S,4R)-1-[(2S)-2-[(1-fluorocyclopropanecarbonyl)amino]-3,3-dimethylbutanoyl]-4-hydroxy-N-[[2-hydroxy-4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide
Molecular Structure CAS # 2306193-99-5, VH032-cyclopropane-F, N-[(1-Fluorocyclopropyl)carbonyl]-3-methyl-L-valyl-(4R)-4-hydroxy-N-[2-hydroxy-4-(4-methyl-1,3-thiazol-5-yl)benzyl]-L-prolinamide, (2S,4R)-1-[(2S)-2-[(1-fluorocyclopropanecarbonyl)amino]-3,3-dimethylbutanoyl]-4-hydroxy-N-[[2-hydroxy-4-(4-methyl-1,3-thiazol-5-yl)phenyl]methyl]pyrrolidine-2-carboxamide
Molecular Formula C26H33FN4O5S
Molecular Weight 532.63
CAS Registry Number 2306193-99-5
SMILES CC1=C(SC=N1)C2=CC(=C(C=C2)CNC(=O)[C@@H]3C[C@H](CN3C(=O)[C@H](C(C)(C)C)NC(=O)C4(CC4)F)O)O
Properties
Density 1.4±0.1 g/cm3, Calc.*
Index of Refraction 1.629, Calc.*
Boiling Point 841.7±65.0 ºC (760 mmHg), Calc.*
Flash Point 462.9±34.3 ºC, Calc.*
* Calculated using Advanced Chemistry Development (ACD/Labs) Software.
Safety Data
Hazard Symbols symbol   GHS07 Warning    Details
Hazard Statements H315-H319-H335    Details
Precautionary Statements P261-P264-P271-P280-P302+P352-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P403+P233-P405-P501    Details
SDS Available
up Discovory and Applicatios
In the realm of chemical innovation, VH032-cyclopropane-F stands as a testament to human ingenuity and scientific progress. This extraordinary substance, discovered at the intersection of chemistry and medicine, has generated great excitement and holds great promise for a wide range of applications. The discovery of VH032-cyclopropane-F stems from intensive research aimed at manipulating cellular processes by chemical means. Its synthesis, developed by a team of pioneering chemists and biologists, represents a major leap forward in targeted pharmacology. The unique structure of the compound, incorporating the cyclopropane-F moiety, enhances its biological activity and specificity, setting it apart from conventional compounds.

In essence, VH032-cyclopropane-F works by selectively inhibiting specific protein-protein interactions that are critical in cell signaling pathways. This precise mode of action provides researchers with unprecedented control over cellular function, opening the way for novel therapeutic interventions. By disrupting key interactions implicated in disease progression, such as cancer and inflammatory diseases, VH032-cyclopropane-F is expected to become a powerful tool in the fight against complex diseases.

The medical implications of VH032-cyclopropane-F are enormous and transformative. Initial studies have highlighted its potential in cancer treatment, where it is expected to inhibit oncogenic pathways without the broad cytotoxic effects of traditional chemotherapy. In addition, its ability to modulate immune responses makes it a potential candidate for the treatment of autoimmune diseases, offering hope for more targeted and effective treatments.

The journey of VH032-cyclopropane-F is filled with promise and challenges. Ongoing research aims to optimize its pharmacokinetics and expand its use across a range of diseases. Challenges include scalability of synthesis, ensuring safety, and finding regulatory pathways for clinical translation.
Market Analysis Reports
List of Reports Available for VH032-cyclopropane-F
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