80 Results for "

phosphonic acid

" in MedChemExpress (MCE) Product Catalog:
Products (80)

80 Results for "phosphonic acid" in MCE Product Catalog:

2
2 Cited Publications
Cat. No.: HY-112853
CAS No.: 66508-37-0
Purity:  99.72%
Synonyms: FR-31564
Target:  

Bacterial Antibiotic

Research Areas:  

Infection

Fosmidomycin sodium salt is a phosphonic acid antibiotic and a antimalarial agent, which is active against both Gram-negative and Gram-positive bacteria.
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1
1 Cited Publications
Cat. No.: HY-W004494
CAS No.: 141120-17-4
Research Areas:  

Others

2-Aminoindan-2-phosphonic acid is an inhibitor of phenylalanine ammonia-lyase (PAL). 2-Aminoindan-2-phosphonic acid reduces the biosynthesis and accumulation of total phenolic compounds in the suspension cell culture system of Cistanche .
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1
1 Cited Publications
Cat. No.: HY-W017692
CAS No.: 1416354-35-2
Research Areas:  

Metabolic Disease

2-Aminoindan-2-phosphonic acid hydrochloride is a competitive phenylalanine ammonia lyase (PAL) inhibitor that significantly decreases the levels of total phenolic compounds and PheGs in plant cultured cells .
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Cat. No.: HY-W006371
CAS No.: 2041-14-7
(2-Aminoethyl)phosphonic acid is an endogenous metabolite and amino acid analog. (2-Aminoethyl)phosphonic acid can be used for the synthesis of biological macromolecules and the preparation of hydrogels .
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Cat. No.: HY-W104477
CAS No.: 7423-96-3
Target:  

Others

Research Areas:  

Metabolic Disease

3-Fluoro-L-tyrosine is a tyrosine analogue, inhibits transamination by tyrosine aminotransferase (TAT). And 3-FluoroL-tyrosine has been shown to be biologically incorporated into proteins in place of tyrosine. 3-Fluoro-L-tyrosine pretends to be the substrate of rat liver tyrosine aminotransferase, markedly disturbs the Tyr-TAT association .
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Cat. No.: HY-W008951
CAS No.: 1429-50-1
Synonyms: EDTMP
Ethylenediaminetetramethylenephosphonic acid (EDTMP) is a bone-targeted chelating agent. Ethylenediaminetetramethylenephosphonic acid sodium‘s phosphonic acid groups possess a unique ability to bind with high affinity to hydroxyapatite in bone, and can form radioactive compounds with 153Sm and 177Lu. Ethylenediaminetetramethylenephosphonic acid is used to study palliative therapy for pain associated with multiple bone metastatic cancers .
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Cat. No.: HY-W035361
CAS No.: 1066-51-9
(Aminomethyl)phosphonic acid is used as a phosphonate agent in wastewater treatment .
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Cat. No.: HY-141307
CAS No.: 1872433-62-9
Target:  

PROTAC Linkers

Research Areas:  

Cancer

m-PEG4-phosphonic acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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Cat. No.: HY-15086
CAS No.: 110347-85-8
Purity:  99.67%
Synonyms: CGS 19755
Target:  

iGluR

Research Areas:  

Neurological Disease

Selfotel (CGS 19755) is a selective and competitive antagonist at N-methyl-D-aspartate (NMDA)-preferring receptor. CGS 19755 inhibits the binding of [3H]-3-(2-carboxypiperazin-4-yl)propyl-1-phosphonic acid to NMDA-type receptors with an IC50 of 50 nM .
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Cat. No.: HY-171615
CAS No.: 46817-52-1
Target:  

Phosphatase

Research Areas:  

Infection

(4-Phenylphenoxy) phosphonic acid is a protein tyrosine phosphatase (PTP) inhibitor (KM: 86 μM). (4-Phenylphenoxy) phosphonic acid can be used in tuberculosis research .
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Cat. No.: HY-W653925
CAS No.: 2727464-25-5
(Aminomethyl)phosphonic acid- 13C, 15N is 13C and 15N-labeled Hexachlorobenzene .
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Cat. No.: HY-Y0643
CAS No.: 18997-19-8
Pivaloyloxymethyl chloride is an organic intermediate used to introduce the pivaloyloxymethyl (POM) protecting group, and it can be prepared from trimethylacetic acid and chloromethyl chlorosulfonate as raw materials. Pivaloyloxymethyl chloride is an alkylating reagent for the synthesis of phosphonic acid prodrugs; the introduction of the hydrophobic POM group enhances the lipid solubility and membrane permeability of molecules. Pivaloyloxymethyl chloride can be used in the synthesis of tetrakis (pivaloyloxymethyl) methylenebisphosphonate, which is a precursor of the pivaloyloxymethyl clodronate prodrug. Pivaloyloxymethyl chloridecan support the synthesis of aryl/pivaloyloxymethyl mixed phosphonate prodrugs of butyrophilin 3A1 ligands .
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Cat. No.: HY-W105694
CAS No.: 13138-33-5
Synonyms: (3-Aminopropyl)phosphonic acid
Target:  

GABA Receptor

Research Areas:  

Neurological Disease

3-Aminopropylphosphonic acid ((3-Aminopropyl)phosphonic acid) is a phosphonic acid analogue of GABA and a GABAB receptor agonist .
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Cat. No.: HY-141319
CAS No.: 1360716-43-3
Target:  

PROTAC Linkers

Research Areas:  

Cancer

Thiol-PEG3-phosphonic acid ethyl ester is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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Cat. No.: HY-W247616
CAS No.: 5424-27-1
Target:  

Bacterial

Research Areas:  

Infection Cancer

(4-Aminobenzyl)phosphonic acid is a bioactive compound with potential anticancer and antibacterial activities. (4-Aminobenzyl)phosphonic acid is widely used in compound synthesis to develop new inhibition methods. Through its unique structure, (4-Aminobenzyl)phosphonic acid can effectively interact with biological targets.
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Cat. No.: HY-130554
CAS No.: 2055016-25-4
Purity:  99.33%
Target:  

PROTAC Linkers

Research Areas:  

Cancer

m-PEG9-phosphonic acid is a PEG-based PROTAC linker can be used in the synthesis of PROTACs.
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Cat. No.: HY-141297
CAS No.: 1446282-44-5
Target:  

PROTAC Linkers

Research Areas:  

Cancer

Bromo-PEG2-phosphonic acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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Cat. No.: HY-141318
CAS No.: 1360716-36-4
Target:  

PROTAC Linkers

Research Areas:  

Cancer

Thiol-PEG3-phosphonic acid is a PEG-based PROTAC linker that can be used in the synthesis of PROTACs .
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Cat. No.: HY-140330
CAS No.: 934985-98-5
Purity:  99.44%
Target:  

PROTAC Linkers

Research Areas:  

Cancer

(10-BRomodecyl)phosphonic acid is an alkyl chain-based PROTAC linker that can be used in the synthesis of PROTACs .
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Cat. No.: HY-128041
CAS No.: 148796-53-6
Synonyms: Hydroxyfarnesyl phosphate
Target:  

Farnesyl Transferase

Research Areas:  

Others

α-hydroxy Farnesyl phosphonic acid is a nonhydrolyzable analog of farnesyl pyrophosphate which acts as a competitive inhibitor of farnesyl transferase (FTase). At concentrations greater than 1 μM, α-hydroxy farnesyl phosphonic acid inhibits the processing of Ras in Ha-ras-transformed NIH3T3 cells.
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