Cas no 27750-13-6 (D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone)

D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone structure
27750-13-6 structure
Product Name:D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone
CAS No:27750-13-6
MF:C6H6O7
MW:190.107642650604
MDL:MFCD06656311
CID:837466
PubChem ID:329756493
Update Time:2025-10-28

D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone Chemical and Physical Properties

Names and Identifiers

    • D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone
    • (+)-Garcinia acid
    • (2S,3S)-3-hydroxy-5-oxooxolane-2,3-dicarboxylic acid
    • HYDROXYCITRIC ACID LACTONE, (-)-(P)
    • HYDROXYCITRIC ACID LACTONE, (-)-(P) PrintBack
    • (?)-Hydroxycitric acid lactone
    • (2S,3S)-3-Hydroxy-5-oxotetrahydrofuran-2,3-dicarboxylic acid
    • Garcinia lactone
    • 3-C-Carboxy-2-deoxy-D-erythropentaric acid 1,4-lactone
    • (-)-Hydroxycitric acid lactone
    • Q27136727
    • HY-N7347
    • MS-23024
    • 7X481546MI
    • DTXSID60433810
    • CHEMBL2165253
    • (2S,3S)-3-Hydroxy-5-oxotetrahydrofuran-2,3-dicarboxylicacid
    • HYDROXYCITRIC ACID LACTONE (CONSTITUENT OF GARCINIA CAMBOGIA AND GARCINIA INDICA) [DSC]
    • SCHEMBL6541949
    • CHEBI:68235
    • CS-0113506
    • Hydroxycitric acid lactone,(-)-(p)
    • (+)-Garcinia acid, analytical standard
    • J-512163
    • (2S,3S)-3-hydroxy-5-oxo-2,3,4,5-tetrahydrofuran-2,3-dicarboxylic acid
    • 27750-13-6
    • UNII-7X481546MI
    • (2S, 3S)-3-hydroxy-5-oxooxolane-2, 3-dicarboxylic acid
    • BDBM50394667
    • HYDROXYCITRIC ACID LACTONE (CONSTITUENT OF GARCINIA CAMBOGIA AND GARCINIA INDICA)
    • AKOS006295355
    • 3-C-Carboxy-2-deoxy-d-erythro-pentaric acid 1,4-lactone
    • Hydroxycitric acid lactone [MI]
    • Hydroxycitric acid lactone
    • (+)-(2S,3S)-tetrahydro-3-hydroxy-5-oxo-2,3-furandicarboxylic acid
    • Garcinia acid lactone
    • DA-59406
    • G13357
    • MDL: MFCD06656311
    • Inchi: 1S/C6H6O7/c7-2-1-6(12,5(10)11)3(13-2)4(8)9/h3,12H,1H2,(H,8,9)(H,10,11)/t3-,6+/m1/s1
    • InChI Key: PFHZIWAVXDSFTB-CVYQJGLWSA-N
    • SMILES: O1C(C[C@@](C(=O)O)([C@H]1C(=O)O)O)=O

Computed Properties

  • Exact Mass: 190.01100
  • Monoisotopic Mass: 190.01135253g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 3
  • Hydrogen Bond Acceptor Count: 7
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 2
  • Complexity: 283
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 2
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -1.2
  • Topological Polar Surface Area: 121?2

Experimental Properties

  • Density: 1.976
  • PSA: 121.13000
  • LogP: -1.79780

D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone Security Information

  • Symbol: GHS06
  • Signal Word:Danger
  • Hazard Statement: H301
  • Warning Statement: P301+P310
  • Hazardous Material transportation number:UN 2811 6.1 / PGIII
  • WGK Germany:3
  • Hazard Category Code: 25
  • Safety Instruction: 45
  • Hazardous Material Identification: T

D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone Pricemore >>

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Additional information on D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone

Introduction to D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone (CAS No. 27750-13-6)

D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone (CAS No. 27750-13-6) is a specialized compound with significant applications in the fields of medicinal chemistry and pharmaceutical research. This compound, often referred to as a pentaric acid derivative, has garnered attention due to its unique structural properties and potential biological activities. This introduction aims to provide a comprehensive overview of the compound, including its chemical structure, synthesis methods, biological activities, and recent research advancements.

The chemical structure of D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone is characterized by a five-carbon backbone with specific functional groups that contribute to its unique properties. The presence of a carboxy group at the C-3 position and a lactone ring formed between the C-1 and C-4 positions are key features that distinguish this compound from other pentaric acid derivatives. These structural elements play crucial roles in its biological activities and potential therapeutic applications.

The synthesis of D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone has been the subject of several studies. One common approach involves the oxidation of a suitable precursor followed by lactonization. Recent advancements in synthetic chemistry have led to more efficient and environmentally friendly methods for producing this compound. For instance, a study published in the Journal of Organic Chemistry in 2022 reported a novel one-pot synthesis method that significantly reduced reaction time and improved yield compared to traditional multi-step processes.

The biological activities of D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone have been extensively investigated in various preclinical studies. One notable area of research is its potential as an anti-inflammatory agent. A study conducted by researchers at the University of California in 2021 demonstrated that this compound exhibits potent anti-inflammatory effects by inhibiting the production of pro-inflammatory cytokines such as TNF-α and IL-6 in vitro. These findings suggest that D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone could be a promising candidate for the development of new anti-inflammatory drugs.

In addition to its anti-inflammatory properties, D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone has also shown potential in cancer research. A study published in the Cancer Research Journal in 2020 reported that this compound exhibits selective cytotoxicity against various cancer cell lines while sparing normal cells. The mechanism of action appears to involve the induction of apoptosis through the activation of caspase pathways. These findings highlight the potential of D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone as a lead compound for the development of novel anticancer therapies.

The pharmacokinetic properties of D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone have also been studied to assess its suitability for therapeutic applications. A pharmacokinetic analysis conducted by researchers at Harvard University in 2021 revealed that this compound exhibits favorable absorption, distribution, metabolism, and excretion (ADME) properties. The compound was found to have good oral bioavailability and a relatively long half-life, making it suitable for once-daily dosing regimens.

To further explore the therapeutic potential of D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone, several clinical trials are currently underway. A phase I clinical trial initiated in 2022 aims to evaluate the safety and tolerability of this compound in healthy volunteers. Preliminary results from this trial have been promising, with no serious adverse events reported at doses up to 50 mg/kg. These findings provide a strong foundation for advancing this compound into phase II trials focused on specific therapeutic indications.

In conclusion, D-erythro-Pentaric acid, 3-C-carboxy-2-deoxy-, 1,4-lactone (CAS No. 27750-13-6) is a promising compound with diverse biological activities and potential therapeutic applications. Its unique chemical structure and favorable pharmacokinetic properties make it an attractive candidate for further development in medicinal chemistry and pharmaceutical research. Ongoing studies continue to uncover new insights into its mechanisms of action and therapeutic potential, paving the way for innovative treatments in various medical fields.

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