5002 Results for "

Drug intermediate

" in MedChemExpress (MCE) Product Catalog:
Products (5002)

5002 Results for "Drug intermediate" in MCE Product Catalog:

22
22 Publications Verification
Cat. No.: HY-W040233
CAS No.: 867-56-1
Synonyms: (S)-2-Hydroxypropanoic acid sodium
L-lactate Sodium (Sodium (S)-2-hydroxypropanoate) is a buildiing block which can be used as a precursor for the production of the bioplastic polymer poly-lactic acid. L-Lactic acid Sodium has antiproliferative activity .
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21
21 Cited Publications
Cat. No.: HY-138300
CAS No.: 1849616-42-7
Purity:  99.93%
Research Areas:  

Others

ALC-0159 presents highly mobile surface PEG chains in a dense brush-like conformation, which can form a hydrophilic barrier, reduce non-specific protein adsorption and macrophage uptake, improve colloidal stability, prolong in vivo circulation time, and affect the cellular uptake of LNPs. ALC-0159 dissociates from the surface of mRNA-LNPs under long-term mechanical oscillation stress, thereby reducing steric hindrance, inducing mRNA-LNP fusion, increasing particle size, and releasing unencapsulated mRNA .
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16
16 Cited Publications
Cat. No.: HY-W105639
CAS No.: 865717-20-0
Target:  

Drug Intermediate

Research Areas:  

Others

L-Lactic acid calcium hydrate is the calcium salt of L-Lactic acid. L-Lactic acid calcium hydrate is a building block that can be used as a precursor for the production of bioplastic polymer polylactic acid .
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8
8 Cited Publications
Cat. No.: HY-N3007
CAS No.: 73692-50-9
Naringenin chalcone is an orally active intermediate in flavonol biosynthesis. Naringenin chalcone induces Apoptosis. Naringenin chalcone inhibits the production of MCP-1 and NO. Naringenin chalcone exhibits anticancer activity against glioblastoma. Naringenin chalcone has anti-inflammatory and anti-allergic properties .
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7
7 Cited Publications
Cat. No.: HY-B0725
CAS No.: 1229-29-4
Doxepin Hydrochloride is an orally active, blood-brain barrier penetrant tricyclic antidepressant with multiple activities including hypnosis, sedation, analgesia and vasodilation. Doxepin Hydrochloride enhances the expression of PSD-95 and synapsin 1 via the PI3K/AKT/mTOR signaling pathway, and is metabolized to DesmethylDoxepin Hydrochloride in vivo. Doxepin Hydrochloride can be used in research related to various diseases such as depression, anxiety, obesity and atopic dermatitis .
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7
7 Cited Publications
Cat. No.: HY-B0725A
CAS No.: 1668-19-5
Doxepin is an orally active, blood-brain barrier penetrant tricyclic antidepressant with multiple activities including hypnosis, sedation, analgesia and vasodilation. Doxepin enhances the expression of PSD-95 and synapsin 1 via the PI3K/AKT/mTOR signaling pathway, and is metabolized to Desmethyldoxepin in vivo. Doxepin can be used in research related to various diseases such as depression, anxiety, obesity and atopic dermatitis .
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5
5 Cited Publications
Cat. No.: HY-17431
CAS No.: 226700-81-8
Synonyms: GW433908G
Research Areas:  

Infection

Fosamprenavir Calcium Salt (GW433908G) is an orally active inhibitor targeting HIV-1 protease and is a prodrug of Amprenavir (HY-17430). Fosamprenavir Calcium Salt is hydrolyzed into Amprenavir (VX-478) by cell phosphatases in the intestinal epithelium. Amprenavir binds to the active site of HIV-1 protease, preventing the processing of viral gag and gag-pol polyprotein precursors, thereby inhibiting the formation of mature infectious virus particles and exerting anti-HIV-1 infection activity. Fosamprenavir Calcium Salt can be used for the study of human immunodeficiency virus (HIV-1) infection .
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5
5 Cited Publications
Cat. No.: HY-78726
CAS No.: 226700-79-4
Synonyms: Amprenavir phosphate; GW 433908
Research Areas:  

Infection

Fosamprenavir is an orally active inhibitor targeting HIV-1 protease and is a prodrug of Amprenavir (HY-17430). Fosamprenavir is hydrolyzed into Amprenavir (VX-478) by cell phosphatases in the intestinal epithelium. Amprenavir binds to the active site of HIV-1 protease, preventing the processing of viral gag and gag-pol polyprotein precursors, thereby inhibiting the formation of mature infectious virus particles and exerting anti-HIV-1 infection activity. Fosamprenavir can be used for the study of human immunodeficiency virus (HIV-1) infection .
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4
4 Cited Publications
Cat. No.: HY-A0104
CAS No.: 9004-65-3
Synonyms: Hypromellose (Viscosity:11250-21000mPa.s); (Hydroxypropyl)methyl cellulose (Viscosity:11250-21000mPa.s); Celacol HPM 5000 (Viscosity:11250-21000mPa.s)
HPMC (Viscosity:11250-21000mPa.s) is a hydrophilic, non-ionic cellulose ether used to form swellable-soluble matrices.
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3
3 Cited Publications
Cat. No.: HY-N7114A
CAS No.: 982-57-0
Chloramphenicol succinate sodium is a prodrug of Chloramphenicol (HY-B0239), acting as a P2Y14R inhibitor with an IC50 of 1.585 nM. Chloramphenicol succinate sodium serves as a competitive substrate and inhibitor of succinate dehydrogenase (SDH), which may account for its toxicity. Chloramphenicol succinate sodium exerts a significant inhibitory effect on colitis. Chloramphenicol succinate sodium can be used in research related to myelosuppression, gray baby syndrome, aplastic anemia, bacterial meningitis and inflammatory bowel disease .
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2
2 Cited Publications
Cat. No.: HY-138558
CAS No.: 1690176-75-0
Purity:  99.79%
Target:  

Drug Intermediate

Research Areas:  

Inflammation/Immunology Cancer

PAR-2-IN intermediate-1 is a drug intermediate that can be used to synthesize inhibitors of the PAR-2 signaling pathway .
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2
2 Cited Publications
Cat. No.: HY-W012860
CAS No.: 104-87-0
p-Tolualdehyde is the active small molecule, that could used as drug intermediate .
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2
2 Cited Publications
Cat. No.: HY-W014589
CAS No.: 96-76-4
Synonyms: 2,4-DTBP
2,4-Di-tert-butylphenol (2,4-DTBP) is an orally active RXRα activator and a human estrogen receptor ligand with anti-inflammatory and antioxidant activities, which can induce apoptosis in tumor cells. 2,4-Di-tert-butylphenol can activate the RXRα subtype in LXRα/RXRα, PPARγ/RXRα, and hormone receptor β/RXRα. 2,4-Di-tert-butylphenol also has antiviral and antifungal activities and has the potential to inhibit Aβ-induced neurotoxicity. 2,4-Di-tert-butylphenol can be used as an intermediate in the preparation of antioxidants and UV stabilizers, and is also used in the manufacture of drugs and fragrances .
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2
2 Cited Publications
Cat. No.: HY-132832
CAS No.: 2079939-05-0
Purity:  99.13%
Synonyms: DRP-104
Target:  

Drug Intermediate

Research Areas:  

Cancer

Sirpiglenastat (DRP-104) is a broad acting glutamine antagonist. Sirpiglenastat has anticancer effects by directly targeting tumor metabolism and simultaneously inducing a potent antitumor immune response .
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2
2 Cited Publications
Cat. No.: HY-W010098
CAS No.: 100-21-0
Terephthalic acid is an isomer and a precursor of polyester PET, which can be used to make clothing and plastics. Terephthalic acid can be used to build skin tumor models .
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2
2 Cited Publications
Cat. No.: HY-33893
CAS No.: 22259-53-6
Indole-3-methanamine is an indole derivative, stress-related metabolite, and also a biosynthetic precursor of Gramine (HY-N0166). The accumulation level of Indole-3-methanamine increases in susceptible barley varieties infected with Bipolaris sorokiniana. Indole-3-methanamine can be used in studies related to barley spot blotch .
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2
2 Cited Publications
Cat. No.: HY-N10616
CAS No.: 90-29-9
Pseudobaptigenin is a natural isoflavone polyphenolic compound. Pseudobaptigenin is generated through the CYP76F319-catalyzed conversion of Calycosin (HY-N0519) and can serve as a precursor for phytoalexin synthesis. Pseudobaptigenin is predicted to have potential as an inhibitor of ER, PR, and HER2. Pseudobaptigenin can be used in research on breast cancer and metabolism-related diseases .
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2
2 Cited Publications
Cat. No.: HY-N12304
CAS No.: 21800-48-6
Xanthalin is a naturally occurring, orally active linear dihydropyranocoumarin. Xanthalin acts as an inhibitor of Spodoptera littoralis neonate larval growth and reduces larval body weight. Xanthalin is used in research related to pest control .
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2
2 Cited Publications
Cat. No.: HY-132987
CAS No.: 2245880-46-8
Purity:  98.57%
Synonyms: ARX-1796; AV-006
Research Areas:  

Infection

Avibactam tomilopil (ARX-1796, AV-006) is an orally active prodrug of Avibactam and a β-lactamase inhibitor. Avibactam tomilopil can be used in the study of diseases such as urinary tract infections .
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2
2 Cited Publications
Cat. No.: HY-Y1213S
CAS No.: 14762-74-4
Carbon- 13C is the 13C labeled Carbon (HY-Y1213). Carbon possesses unique physicochemical properties such as electrical and structural characteristics, making it a core material in the field of fuel cells. Carbon also serves as a pharmaceutical excipient and can be used in the synthesis of other compounds .
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