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Sugars and Glycoside-Containing Natural Products

Date：June 02 2026Web Page No：549088

Institute of Microbial Chemistry

We provide natural products containing sugar or glycosidic structures selected from biologically active microbial metabolites that were discovered and isolated at the Institute of Microbial Chemistry (BIKAKEN). Compounds containing sugar moieties are often highly water-soluble, and some are known to exhibit improved bioavailability and enhanced stability. Natural products possessing unique sugar structures display highly intriguing biological activities and have attracted considerable attention in the research field.

* SDF (Structure Data Format) files of the compounds are available.
* Please do not hesitate to contact Funakoshi if you need a Structure Data Format (SDF) file and/or bulk purchase (large quantity) of the compounds.
* This product is for research use only.


Product Table

Click the compound name to view detailed information, click the product code to view the price list, and click the chemical structure to enlarge the image.

Product Name Chemical Structure Biological Activity Product Code
Bagougeramine A Bagougeramine Aの化学構造式 Potent acaricidal activity against the two-spotted spider mite, broad antimicrobial activity against bacteria and fungi 18206
Benanomicin A Benanomicin Aの化学構造式 Antifungal activity. Excellent efficacy in a mouse model of Pneumocystis carinii pneumonia 02966
Benanomicin B Benanomicin Bの化学構造式 Inhibition of HIV-1 infection in human T cells and antimicrobial activity 02968
COTC COTCの化学構造式 Alkaline phosphodiesterase, glyoxalase 1 (GLO1), and glyoxalase 2 (GLO2) inhibitory activities 14675
6-epi-COTC 6-epi-COTCの化学構造式 Cytotoxicity against the human lung cancer cell lines A549 and H460 14698
Heliquinomycin Heliquinomycinの化学構造式 Inhibition of DNA helicase, topoisomerases I and II, and human tumor cell growth 10665
Heparastatin SF4 Heparastatin SF4の化学構造式 Inhibition of heparanase and β-glucuronidase 11829
IMCTA-C14 IMCTA-C14の化学構造式 High protein extraction capability 15613
Lentztrehalose A Lentztrehalose Aの化学構造式 Trehalase resistance, anticancer activity, and bone-strengthening and anti-obesity effects in a postmenopausal mouse model 14678
Lentztrehalose B Lentztrehalose Bの化学構造式 Resistance to trehalase 14679
Lentztrehalose C Lentztrehalose Cの化学構造式 Resistance to trehalase 14680
Minosaminomycin Minosaminomycinの化学構造式 Inhibition of mycobacterial growth and bacterial protein synthesis 02872
Oxanosine Oxanosineの化学構造式 Inhibition of HeLa and L1210 cell proliferation, GMP synthetase inhibition, and anti-HIV activity 00762
4-Trehalosamine 4-Trehalosamineの化学構造式 Trehalase resistance, anti-staling effect on starch, and humectant and protective agent with pH-buffering capacity 15612

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Product Information

[Date : June 03 2026 00:13]

Detail Product Name Product Code Supplier Size Price
Bagougeramine A Formate <Acaricidal>
DatasheetThis may not be the latest data sheet. 		18206 IMCInstitute of Microbial Chemistry 1 mg $500

Description M.W.: 576.524 Purity : >98% (HPLC) Molecular Formula : C17H28N10O7・2HCO2H (formate salt form) Solubility : Soluble in H2O Slightly soluble in DMSO, Insoluble in MeOH Bagougeramine A exhibited acaricidal activity against the two spotted spier mite (Tetranychus urticae) and had broad antimicrobial activity against bacteria and fungi. This product is supplied as the formate from.
Storage -20°C CAS 104840-35-9 (salt free form)
Link

Bagougeramine A (Formate)
Natural bioactive compounds from microorganisms for supporting of fertilizer and pesticide researches

Benanomicin A, Antifungal via Binding to Mannan
DatasheetThis may not be the latest data sheet. 		02966 IMCInstitute of Microbial Chemistry 1 mg $500

Description M.W.: 827.74 Purity : > 90％ (HPLC) Molecular Formula : C39H41NO19 Solubility : Soluble in DMSO and DMF, Poorly soluble in MeOH and CHCl3 Insoluble in H2O, Antimicrobial activity (MIC) : Cryptococcus neoformans F-10 0.6~1.25 μg/ml, Cryptococcus laurenti 0.63 μg/ml, Rhodotorula rubra 0.63 μg/ml, Tricosporon cutaneum 1.25~5 μg/ml. Benanomicin A is isolated from Actinomadura sp. MH193-16F4. This compound exhibits excellent therapeutic efficacy against in a Pneumocystis carinii-infected mouse model by intraperitoneal administration at 10mg/kg/day. In addition, this compound also has antimycotic activities via binding to mannan in the cell walls of fungi. It is recently reported that this compound has been utilized to prepare mannan cell walls by the lectin-like functionality of it.
Storage -20°C CAS 116249-65-1
Link

Benanomicin A
Bioactive Compounds
Natural bioactive compounds from microorganisms for supporting of fertilizer and pesticide researches

Benanomicin B, Antifungal
DatasheetThis may not be the latest data sheet. 		02968 IMCInstitute of Microbial Chemistry 1 mg $500

Description M.W.: 826.761 Purity : > 90％ (HPLC) Molecular Formula : C39H42N2O18 Solubility : Soluble in DMSO, Insoluble in H2O, Benanomicin B is an antibiotic isolated from the culture fluid of Actinomadura sp. MH193-16F4. This compound prevented HIV-1 infection to human T-cells and syncytium formation. In addition, the natural compound is also reported antifungal and antibacterial activities against Candida, Cryptococcus and Saccharomyces, etc.
Storage -20°C CAS 116249-66-2 (free form)
Link

Benanomicin B
Bioactive Compounds
Natural bioactive compounds from microorganisms for supporting of fertilizer and pesticide researches

COTC, Glyoxalase-I Inhibitor
DatasheetThis may not be the latest data sheet. 		14675 IMCInstitute of Microbial Chemistry 1 mg $500

Description M.W.: 242.227 Purity : >90% (HPLC) Molecular Formula : C11H14O6 Solubility : Soluble in MeOH, DMSO, and H2O, Insoluble in hexane, blocks enzymatic activity of alkaline phosphodiesterase derived from murine lymphoblastoma L5178Y cells (IC50: 60ug/ml), glyoxylase I in rat liver crude (IC50: 1.8 mM), and in yeast (IC50: 1.4 mM)
Storage -20°C CAS 57449-30-6
Link

COTC
Bioactive Compounds

6-epi-COTC, Cytotoxic
DatasheetThis may not be the latest data sheet. 		14698 IMCInstitute of Microbial Chemistry 1 mg $500

Description M.W.: 242.227 Purity : >98% (HPLC) Molecular Formula : C11H14O6 Solubility : Soluble in H2O, DMSO, 6-epi-COTC was isolated from Streptomyces griseosporeus as same as COTC. This compound is a diastereomer of COTC and showed cytotoxic activity towards lung cancer cell lines A549 and H460.
Storage -20°C CAS 959150-61-9
Link

Bioactive Compounds
6-epi-COTC [CAS: 959150-61-9]

Heliquinomycin, DNA Helicase Inhibitor
DatasheetThis may not be the latest data sheet. 		10665 IMCInstitute of Microbial Chemistry 1 mg $500

Description M.W.: 698.5811 Purity : > 80％ (HPLC) Molecular Formula : C33H30O17 Solubility : Soluble in EtOAc, EtOH, and DMSO, Insoluble in H2O, and Hexane. Heliquinomycin is a natural product derived from actinomycetes and inhibits DNA helicase. In addition, it inhibits growth of human tumor cell lines such as HeLa S3, KB, LS180, K562, and HL60. In cell culture, this compound also inhibits both DNA and RNA synthesis but do not inhibit protein synthesis. It was reported that HeLa S3 growth was arrested at G2/M phase by Heliquinomycin treatment.
Storage -20°C CAS 178182-49-5
Link

Heliquinomycin
Bioactive Compounds
Natural compound Product List

Heparastatin (Hydrochloride), SF4 Hydrochloride, Heparanase Inhibitor
DatasheetThis may not be the latest data sheet. 		11829 IMCInstitute of Microbial Chemistry 1 mg $500

Description Molecular Formula: C8H11F3N2O5・HCl, Molecular Weight: 308.64, Heparastatin (SF4) inhibits recombinant human heparanase from human melanoma A375M cells transfected with pBK-CMV expression vectors containing the heparanase cDNA with IC50 1.02μM.
Storage -20°C CAS 153758-26-0 (hydrochloride salt), 153758-25-9 (salt free form)
Link

Heparastatin (SF4) Hydrochloride
Bioactive Compounds

IMCTA-C14 (trifluoroacetate), High Protein Extraction and Solubilization Activities
DatasheetThis may not be the latest data sheet. 		15613 IMCInstitute of Microbial Chemistry 5 mg $500

Description M.W.: 651.714 Purity : >90% (qNMR) Molecular Formula : C26H51NO10・CF3COOH Solubility : Soluble in MeOH, H2O, and DMSO IMCTA-C14 is N-tetradecyl derivative from 4-Trehalosamine, and showed high efficiency of protein extraction and solubilization without denaturing proteins. It was reported that this compound is stable against trehalases in mammalian and was not observed hydrolysis by porcine one.
Storage -20°C CAS
Link

IMCTA-C14 (Trifluoroacetate)

Lentztrehalose A, Trehalase Resistant
DatasheetThis may not be the latest data sheet. 		14678 IMCInstitute of Microbial Chemistry 25 mg $500

Description M.W.: 444.430 Purity : >80% (qNMR) Molecular Formula : C17H32O13 Solubility : Soluble in DMSO, MeOH, and H2O Insoluble in hexane Lentztrehalose A is a biologically stable analog of trehalose harboring resistance of treharease and various microbes which can degrade general trehalose. The trehalose analog shows trehalose like bioactivities, such as bone reinforcement and anti-obesity effect in a postmenopausal mouse model.
Storage -20°C CAS 1609356-99-1
Link

Bioactive Compounds
Lentztrehalose A
Lentztrehalose A and its analogues B, C

Lentztrehalose B, Trehalase Resistant
DatasheetThis may not be the latest data sheet. 		14679 IMCInstitute of Microbial Chemistry 25 mg $500

Description M.W.: 410.416 Purity : >80% (qNMR) Molecular Formula : C17H30O11 Solubility : Soluble in DMSO, MeOH, and H2O Insoluble in hexane Lentztrehalose B is a biologically stable analog of trehalose harboring resistance of treharease and various microbes which can degrade general trehalose. After the oral administration of the trehalose analog to mice, it showed much better blood concentration compared to that of trehalose.
Storage -20°C CAS 1808096-67-4
Link

Bioactive Compounds
Lentztrehalose B
Lentztrehalose A and its analogues B, C

Lentztrehalose C, Trehalase Resistant
DatasheetThis may not be the latest data sheet. 		14680 IMCInstitute of Microbial Chemistry 25 mg $500

Description M.W.: 426.415 Purity : >75% (qNMR) Molecular Formula : C17H30O12 Solubility : Soluble in DMSO, MeOH, and H2O Insoluble in hexane Lentztrehalose C is a biologically stable analog of trehalose harboring resistance of treharease and various microbes which can degrade general trehalose. After the oral administration of the trehalose analog to mice, it showed much better blood concentration compared to that of trehalose.
Storage -20°C CAS 1808096-68-5
Link

Bioactive Compounds
Lentztrehalose C
Lentztrehalose A and its analogues B, C

Minosaminomycin, Bacterial Protein Synthesis Inhibitor
DatasheetThis may not be the latest data sheet. 		02872 IMCInstitute of Microbial Chemistry 1 mg $500

Description M.W.: 618.689 Purity : >98％ (HPLC) Molecular Formula : C25H46N8O10 Solubility : Soluble in MeOH, DMSO, and H2O, Insoluble in Hexane. Minosaminomycin inhibits phage f2 RNA-directed protein synthesis in a cell-free system of Escherichia coli by 50% at 0.2 µM. It was also reported that minimum inhibitory concentrations of the bioactive compound were determined as 1.56 µg/ml for Mycobacterium smegmatis ATCC 607 and 6.25 µg/ml for Mycobacterium phlei, respectively.
Storage -20°C CAS 51746-09-9
Link

Minosaminomycin
Bioactive Compounds

Oxanosine, Antitumor, GMP Synthase Inhibitor
DatasheetThis may not be the latest data sheet. 		00762 IMCInstitute of Microbial Chemistry 1 mg $500

Description M.W.: 284.23 Purity : > 98％ (HPLC) Molecular Formula : C10H12N4O6 Solubility : Soluble in H2O, Methanol, and DMSO, Insoluble in CHCl3. Inhibitory activity of leukemia L210 : IC50=1.0 μg/ml, Competitive inhibitory activity of GMP synthase : Ki=7.4x10-4 M. Oxanosine was isolated from culture broth of Streptomyces capreolus MG265-CF3 and was reported as a novel nucleoside. It was also reported that this compound has an inhibitory activity of HIV replication and leukemia L1210 cell growth.
Storage -20°C CAS 80394-72-5
Link

Oxanosine
Bioactive Compounds

4-Trehalosamine, Trehalase Resistant, Preventive Effect on Starch Retrogradation
DatasheetThis may not be the latest data sheet. 		15612 IMCInstitute of Microbial Chemistry 25 mg $500

Description M.W.: 341.313 Purity : >90% (qNMR) Molecular Formula : C12H23NO10 Solubility : Soluble in MeOH, H2O, and DMSO 4-Trehalosamine is a trehalose analogue having trehalase tolerance. This analogue showed strong buffering action at neutral pH similar to that of Tris buffer. In addition, it was reported that this compound had protective effect from desiccation and inhibitory activity of starch retrogradation, which were similar or slightly stronger than trehalose.
Storage -20°C CAS 51855-99-3
Link

4-Trehalosamine

[Date : June 03 2026 00:13]

Bagougeramine A Formate <Acaricidal>

DatasheetThis may not be the latest data sheet.


  • Product Code: 18206
  • Supplier: IMC
  • Size: 1mg
  • Price: $500

Description M.W.: 576.524 Purity : >98% (HPLC) Molecular Formula : C17H28N10O7・2HCO2H (formate salt form) Solubility : Soluble in H2O Slightly soluble in DMSO, Insoluble in MeOH Bagougeramine A exhibited acaricidal activity against the two spotted spier mite (Tetranychus urticae) and had broad antimicrobial activity against bacteria and fungi. This product is supplied as the formate from.
Storage -20°C CAS 104840-35-9 (salt free form)
Link

Bagougeramine A (Formate)
Natural bioactive compounds from microorganisms for supporting of fertilizer and pesticide researches

Benanomicin A, Antifungal via Binding to Mannan

DatasheetThis may not be the latest data sheet.


  • Product Code: 02966
  • Supplier: IMC
  • Size: 1mg
  • Price: $500

Description M.W.: 827.74 Purity : > 90％ (HPLC) Molecular Formula : C39H41NO19 Solubility : Soluble in DMSO and DMF, Poorly soluble in MeOH and CHCl3 Insoluble in H2O, Antimicrobial activity (MIC) : Cryptococcus neoformans F-10 0.6~1.25 μg/ml, Cryptococcus laurenti 0.63 μg/ml, Rhodotorula rubra 0.63 μg/ml, Tricosporon cutaneum 1.25~5 μg/ml. Benanomicin A is isolated from Actinomadura sp. MH193-16F4. This compound exhibits excellent therapeutic efficacy against in a Pneumocystis carinii-infected mouse model by intraperitoneal administration at 10mg/kg/day. In addition, this compound also has antimycotic activities via binding to mannan in the cell walls of fungi. It is recently reported that this compound has been utilized to prepare mannan cell walls by the lectin-like functionality of it.
Storage -20°C CAS 116249-65-1
Link

Benanomicin A
Bioactive Compounds
Natural bioactive compounds from microorganisms for supporting of fertilizer and pesticide researches

Benanomicin B, Antifungal

DatasheetThis may not be the latest data sheet.


  • Product Code: 02968
  • Supplier: IMC
  • Size: 1mg
  • Price: $500

Description M.W.: 826.761 Purity : > 90％ (HPLC) Molecular Formula : C39H42N2O18 Solubility : Soluble in DMSO, Insoluble in H2O, Benanomicin B is an antibiotic isolated from the culture fluid of Actinomadura sp. MH193-16F4. This compound prevented HIV-1 infection to human T-cells and syncytium formation. In addition, the natural compound is also reported antifungal and antibacterial activities against Candida, Cryptococcus and Saccharomyces, etc.
Storage -20°C CAS 116249-66-2 (free form)
Link

Benanomicin B
Bioactive Compounds
Natural bioactive compounds from microorganisms for supporting of fertilizer and pesticide researches

COTC, Glyoxalase-I Inhibitor

DatasheetThis may not be the latest data sheet.


  • Product Code: 14675
  • Supplier: IMC
  • Size: 1mg
  • Price: $500

Description M.W.: 242.227 Purity : >90% (HPLC) Molecular Formula : C11H14O6 Solubility : Soluble in MeOH, DMSO, and H2O, Insoluble in hexane, blocks enzymatic activity of alkaline phosphodiesterase derived from murine lymphoblastoma L5178Y cells (IC50: 60ug/ml), glyoxylase I in rat liver crude (IC50: 1.8 mM), and in yeast (IC50: 1.4 mM)
Storage -20°C CAS 57449-30-6
Link

COTC
Bioactive Compounds

6-epi-COTC, Cytotoxic

DatasheetThis may not be the latest data sheet.


  • Product Code: 14698
  • Supplier: IMC
  • Size: 1mg
  • Price: $500

Description M.W.: 242.227 Purity : >98% (HPLC) Molecular Formula : C11H14O6 Solubility : Soluble in H2O, DMSO, 6-epi-COTC was isolated from Streptomyces griseosporeus as same as COTC. This compound is a diastereomer of COTC and showed cytotoxic activity towards lung cancer cell lines A549 and H460.
Storage -20°C CAS 959150-61-9
Link

Bioactive Compounds
6-epi-COTC [CAS: 959150-61-9]

Heliquinomycin, DNA Helicase Inhibitor

DatasheetThis may not be the latest data sheet.


  • Product Code: 10665
  • Supplier: IMC
  • Size: 1mg
  • Price: $500

Description M.W.: 698.5811 Purity : > 80％ (HPLC) Molecular Formula : C33H30O17 Solubility : Soluble in EtOAc, EtOH, and DMSO, Insoluble in H2O, and Hexane. Heliquinomycin is a natural product derived from actinomycetes and inhibits DNA helicase. In addition, it inhibits growth of human tumor cell lines such as HeLa S3, KB, LS180, K562, and HL60. In cell culture, this compound also inhibits both DNA and RNA synthesis but do not inhibit protein synthesis. It was reported that HeLa S3 growth was arrested at G2/M phase by Heliquinomycin treatment.
Storage -20°C CAS 178182-49-5
Link

Heliquinomycin
Bioactive Compounds
Natural compound Product List

Heparastatin (Hydrochloride), SF4 Hydrochloride, Heparanase Inhibitor

DatasheetThis may not be the latest data sheet.


  • Product Code: 11829
  • Supplier: IMC
  • Size: 1mg
  • Price: $500

Description Molecular Formula: C8H11F3N2O5・HCl, Molecular Weight: 308.64, Heparastatin (SF4) inhibits recombinant human heparanase from human melanoma A375M cells transfected with pBK-CMV expression vectors containing the heparanase cDNA with IC50 1.02μM.
Storage -20°C CAS 153758-26-0 (hydrochloride salt), 153758-25-9 (salt free form)
Link

Heparastatin (SF4) Hydrochloride
Bioactive Compounds

IMCTA-C14 (trifluoroacetate), High Protein Extraction and Solubilization Activities

DatasheetThis may not be the latest data sheet.


  • Product Code: 15613
  • Supplier: IMC
  • Size: 5mg
  • Price: $500

Description M.W.: 651.714 Purity : >90% (qNMR) Molecular Formula : C26H51NO10・CF3COOH Solubility : Soluble in MeOH, H2O, and DMSO IMCTA-C14 is N-tetradecyl derivative from 4-Trehalosamine, and showed high efficiency of protein extraction and solubilization without denaturing proteins. It was reported that this compound is stable against trehalases in mammalian and was not observed hydrolysis by porcine one.
Storage -20°C CAS
Link

IMCTA-C14 (Trifluoroacetate)

Lentztrehalose A, Trehalase Resistant

DatasheetThis may not be the latest data sheet.


  • Product Code: 14678
  • Supplier: IMC
  • Size: 25mg
  • Price: $500

Description M.W.: 444.430 Purity : >80% (qNMR) Molecular Formula : C17H32O13 Solubility : Soluble in DMSO, MeOH, and H2O Insoluble in hexane Lentztrehalose A is a biologically stable analog of trehalose harboring resistance of treharease and various microbes which can degrade general trehalose. The trehalose analog shows trehalose like bioactivities, such as bone reinforcement and anti-obesity effect in a postmenopausal mouse model.
Storage -20°C CAS 1609356-99-1
Link

Bioactive Compounds
Lentztrehalose A
Lentztrehalose A and its analogues B, C

Lentztrehalose B, Trehalase Resistant

DatasheetThis may not be the latest data sheet.


  • Product Code: 14679
  • Supplier: IMC
  • Size: 25mg
  • Price: $500

Description M.W.: 410.416 Purity : >80% (qNMR) Molecular Formula : C17H30O11 Solubility : Soluble in DMSO, MeOH, and H2O Insoluble in hexane Lentztrehalose B is a biologically stable analog of trehalose harboring resistance of treharease and various microbes which can degrade general trehalose. After the oral administration of the trehalose analog to mice, it showed much better blood concentration compared to that of trehalose.
Storage -20°C CAS 1808096-67-4
Link

Bioactive Compounds
Lentztrehalose B
Lentztrehalose A and its analogues B, C

Lentztrehalose C, Trehalase Resistant

DatasheetThis may not be the latest data sheet.


  • Product Code: 14680
  • Supplier: IMC
  • Size: 25mg
  • Price: $500

Description M.W.: 426.415 Purity : >75% (qNMR) Molecular Formula : C17H30O12 Solubility : Soluble in DMSO, MeOH, and H2O Insoluble in hexane Lentztrehalose C is a biologically stable analog of trehalose harboring resistance of treharease and various microbes which can degrade general trehalose. After the oral administration of the trehalose analog to mice, it showed much better blood concentration compared to that of trehalose.
Storage -20°C CAS 1808096-68-5
Link

Bioactive Compounds
Lentztrehalose C
Lentztrehalose A and its analogues B, C

Minosaminomycin, Bacterial Protein Synthesis Inhibitor

DatasheetThis may not be the latest data sheet.


  • Product Code: 02872
  • Supplier: IMC
  • Size: 1mg
  • Price: $500

Description M.W.: 618.689 Purity : >98％ (HPLC) Molecular Formula : C25H46N8O10 Solubility : Soluble in MeOH, DMSO, and H2O, Insoluble in Hexane. Minosaminomycin inhibits phage f2 RNA-directed protein synthesis in a cell-free system of Escherichia coli by 50% at 0.2 µM. It was also reported that minimum inhibitory concentrations of the bioactive compound were determined as 1.56 µg/ml for Mycobacterium smegmatis ATCC 607 and 6.25 µg/ml for Mycobacterium phlei, respectively.
Storage -20°C CAS 51746-09-9
Link

Minosaminomycin
Bioactive Compounds

Oxanosine, Antitumor, GMP Synthase Inhibitor

DatasheetThis may not be the latest data sheet.


  • Product Code: 00762
  • Supplier: IMC
  • Size: 1mg
  • Price: $500

Description M.W.: 284.23 Purity : > 98％ (HPLC) Molecular Formula : C10H12N4O6 Solubility : Soluble in H2O, Methanol, and DMSO, Insoluble in CHCl3. Inhibitory activity of leukemia L210 : IC50=1.0 μg/ml, Competitive inhibitory activity of GMP synthase : Ki=7.4x10-4 M. Oxanosine was isolated from culture broth of Streptomyces capreolus MG265-CF3 and was reported as a novel nucleoside. It was also reported that this compound has an inhibitory activity of HIV replication and leukemia L1210 cell growth.
Storage -20°C CAS 80394-72-5
Link

Oxanosine
Bioactive Compounds

4-Trehalosamine, Trehalase Resistant, Preventive Effect on Starch Retrogradation

DatasheetThis may not be the latest data sheet.


  • Product Code: 15612
  • Supplier: IMC
  • Size: 25mg
  • Price: $500

Description M.W.: 341.313 Purity : >90% (qNMR) Molecular Formula : C12H23NO10 Solubility : Soluble in MeOH, H2O, and DMSO 4-Trehalosamine is a trehalose analogue having trehalase tolerance. This analogue showed strong buffering action at neutral pH similar to that of Tris buffer. In addition, it was reported that this compound had protective effect from desiccation and inhibitory activity of starch retrogradation, which were similar or slightly stronger than trehalose.
Storage -20°C CAS 51855-99-3
Link

4-Trehalosamine


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