α-Cyclodextrin - ≥98.0%(HPLC), high purity , CAS No.10016-20-3

32 Citations
  • ≥98%(HPLC)
Item Number
C106777
Grouped product items
SKUSizeAvailabilityPrice Qty
C106777-5g
5g
In stock
$63.90
C106777-25g
25g
In stock
$126.90
C106777-100g
100g
In stock
$319.90
C106777-500g
500g
In stock
$1,119.90

Non-reducing cyclic saccharide consisting of six α-1,4-linked D-glucopyranosyl units.

Basic Description

SynonymsCyclohexaamylose | Schardinger α-Dextrin | Schardinger alpha-dextrin | alpha-Cyclodextrin | α-Schardinger dextrin | Cyclomaltohexaose
Specifications & Purity≥98%(HPLC)
Biochemical and Physiological MechanismsNon-reducing cyclic saccharide consisting of six α-1,4-linked D-glucopyranosyl units produced by the action of cyclodextrin glucosyltransferase (CGTase, EC 2.4.1.19) on hydrolyzed starch.
Shipped InNormal
NoteWherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Refer to SDS for further information Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

α-Cyclodextrin can be used:

· In fabricating reversible supramolecular assemblies.

· As a modifier to enhance the solubility of oleic acid stabilized nanoparticles.

· In the preparation of polyrotaxanes with ply(ethylene glycol).

· In the synthesis of cationic star polymers with oligoethylenimine.


Associated Targets(Human)

PDE5A Tclin Phosphodiesterase 5A (5113 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EGFR Tclin Epidermal growth factor receptor erbB1 (33727 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CA2 Tclin Carbonic anhydrase II (17698 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR1 Tclin Estrogen receptor alpha (17718 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HMGCR Tclin HMG-CoA reductase (2475 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
INSR Tclin Insulin receptor (5558 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PGR Tclin Progesterone receptor (8562 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB2 Tclin Beta-2 adrenergic receptor (11824 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM2 Tclin Muscarinic acetylcholine receptor M2 (10671 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRB1 Tclin Beta-1 adrenergic receptor (6630 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1A Tclin Serotonin 1a (5-HT1a) receptor (14969 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA2A Tclin Alpha-2a adrenergic receptor (9450 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AR Tclin Androgen Receptor (11781 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM1 Tclin Muscarinic acetylcholine receptor M1 (12690 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACE Tclin Angiotensin-converting enzyme (1423 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
TSHR Tclin Thyroid stimulating hormone receptor (29986 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MAOA Tclin Monoamine oxidase A (11911 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CNR1 Tclin Cannabinoid CB1 receptor (20913 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD1 Tclin Dopamine D1 receptor (9720 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD4 Tchem Dopamine D4 receptor (7907 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS1 Tclin Cyclooxygenase-1 (9233 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A2 Tclin Norepinephrine transporter (10102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH2 Tclin Histamine H2 receptor (5428 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1D Tclin Alpha-1d adrenergic receptor (4171 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR1B Tclin Serotonin 1b (5-HT1b) receptor (2801 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2A Tclin Serotonin 2a (5-HT2a) receptor (14758 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR2C Tclin Serotonin 2c (5-HT2c) receptor (11471 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CALCR Tclin Calcitonin receptor (2215 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A4 Tclin Serotonin transporter (12625 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1A Tclin Alpha-1a adrenergic receptor (8359 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PTGS2 Tclin Cyclooxygenase-2 (13999 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HRH1 Tclin Histamine H1 receptor (7573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADRA1B Tclin Alpha-1b adrenergic receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRM1 Tclin Mu opioid receptor (19785 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD3 Tclin Dopamine D3 receptor (14368 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AVPR1A Tclin Vasopressin V1a receptor (5412 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRD1 Tclin Delta opioid receptor (15096 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
OPRK1 Tclin Kappa opioid receptor (16155 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ESR2 Tclin Estrogen receptor beta (9272 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CYSLTR1 Tclin Cysteinyl leukotriene receptor 1 (2118 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ERBB2 Tclin Receptor protein-tyrosine kinase erbB-2 (7851 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM4 Tclin Muscarinic acetylcholine receptor M4 (6041 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CHRM5 Tclin Muscarinic acetylcholine receptor M5 (4677 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Associated Targets(non-human)

Agtr2 Angiotensin II type 2 (AT-2) receptor (803 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mc4r Melanocortin receptor 4 (1205 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ltc4s Leukotriene C4 synthase (1 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Sigmar1 Sigma opioid receptor (160 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Npy1r Neuropeptide Y receptor type 1 (8 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cckar Cholecystokinin A receptor (90 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mapk1 MAP kinase ERK2 (650 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Glra2 Glycine receptor (1745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Names and Identifiers

Pubchem Sid488189830
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488189830
IUPAC Name (1S,3R,5R,6S,8R,10R,11S,13R,15R,16S,18R,20R,21S,23R,25R,26S,28R,30R,31R,32R,33R,34R,35R,36R,37R,38R,39R,40R,41R,42R)-5,10,15,20,25,30-hexakis(hydroxymethyl)-2,4,7,9,12,14,17,19,22,24,27,29-dodecaoxaheptacyclo[26.2.2.23,6.28,11.213,16.218,21.223,26]dotetracontane-31,32,33,34,35,36,37,38,39,40,41,42-dodecol
INCHI InChI=1S/C36H60O30/c37-1-7-25-13(43)19(49)31(55-7)62-26-8(2-38)57-33(21(51)15(26)45)64-28-10(4-40)59-35(23(53)17(28)47)66-30-12(6-42)60-36(24(54)18(30)48)65-29-11(5-41)58-34(22(52)16(29)46)63-27-9(3-39)56-32(61-25)20(50)14(27)44/h7-54H,1-6H2/t7-,8-,9-,10-,11-,12-,13-,14-,15-,16-,17-,18-,19-,20-,21-,22-,23-,24-,25-,26-,27-,28-,29-,30-,31-,32-,33-,34-,35-,36-/m1/s1
InChi Key HFHDHCJBZVLPGP-RWMJIURBSA-N
Canonical SMILES C(C1C2C(C(C(O1)OC3C(OC(C(C3O)O)OC4C(OC(C(C4O)O)OC5C(OC(C(C5O)O)OC6C(OC(C(C6O)O)OC7C(OC(O2)C(C7O)O)CO)CO)CO)CO)CO)O)O)O
Isomeric SMILES C([C@@H]1[C@@H]2[C@@H]([C@H]([C@H](O1)O[C@@H]3[C@H](O[C@@H]([C@@H]([C@H]3O)O)O[C@@H]4[C@H](O[C@@H]([C@@H]([C@H]4O)O)O[C@@H]5[C@H](O[C@@H]([C@@H]([C@H]5O)O)O[C@@H]6[C@H](O[C@@H]([C@@H]([C@H]6O)O)O[C@@H]7[C@H](O[C@H](O2)[C@@H]([C@H]7O)O)CO)CO)CO)CO)CO)O)O)O
WGK Germany 3
PubChem CID 444913
Molecular Weight 972.84
Beilstein 79627

Certificates

Certificate of Analysis(COA)

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17 results found

Lot NumberCertificate TypeDateItem
F2424106Certificate of AnalysisJun 07, 2024 C106777
F2424105Certificate of AnalysisJun 07, 2024 C106777
F2411087Certificate of AnalysisApr 28, 2024 C106777
C2401168Certificate of AnalysisFeb 21, 2024 C106777
C2401169Certificate of AnalysisFeb 21, 2024 C106777
C2401170Certificate of AnalysisFeb 21, 2024 C106777
C2401167Certificate of AnalysisFeb 21, 2024 C106777
D2321813Certificate of AnalysisNov 25, 2022 C106777
D2321907Certificate of AnalysisNov 25, 2022 C106777
D2321815Certificate of AnalysisNov 25, 2022 C106777
D2321812Certificate of AnalysisNov 25, 2022 C106777
D2321794Certificate of AnalysisNov 25, 2022 C106777
D2321766Certificate of AnalysisNov 25, 2022 C106777
D2321765Certificate of AnalysisNov 25, 2022 C106777
K2203189Certificate of AnalysisNov 10, 2022 C106777
I2202455Certificate of AnalysisJul 27, 2022 C106777
I2202458Certificate of AnalysisJul 27, 2022 C106777

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Chemical and Physical Properties

SolubilitySoluble in water (145 mg/ml at 20 °C). Insoluble in ethanol, and acetone.
Specific Rotation[α]149° (C=1,H2O)
Melt Point(°C)278°C

Safety and Hazards(GHS)

Signal Warning
Hazard Statements

H302:Harmful if swallowed

Precautionary Statements

P305+P351+P338:IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses if present and easy to do - continue rinsing.

P280:Wear protective gloves/protective clothing/eye protection/face protection.

WGK Germany 3
Merck Index 2718

Related Documents

Citations of This Product

1. You Zhang, Wenzhong Ma, Jing Zhong, Zhou Zhou, Haicun Yang, Zheng Cao, Shuo Wang.  (2024)  Rapid shape recovery and remodeling by tuning the topology of polycaprolactone-based polymer networks.  POLYMER,  292  (126641).  [PMID:]
2. Lin Wang, Fangkun Xiao, Haochen Ge, Yunbo Tong, Congjie Gao, Guiru Zhu.  (2024)  The fabrication of thin-film nanocomposite membrane for organic solvent forward osmosis via host-guest chemistry of α-cyclodextrin.  DESALINATION,  574  (117247).  [PMID:]
3. Hengjun Zhou, Chenyu Liu, Simiao Yu, Farishta Shafiq, Weihong Qiao.  (2024)  Amphiphilic conjugates for solubilization of paclitaxel as efficient drug carriers based on hyaluronic acid and cyclodextrins.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,  683  (133026).  [PMID:]
4. Si-Qi Nie, Yun-Yue Yuan, Hui-Min Zeng, Zhan-Guo Jiang, Cai-Hong Zhan.  (2023)  Homohelical Self-Assembly of Trimer of α-Cyclodextrin and Octamolybdate.  INORGANIC CHEMISTRY,  62  (46): (19153–19158).  [PMID:37934703]
5. Cai-yun LIU, Lu-lu WU, Shu-yue FAN, Yong-sheng TAO, Yun-kui LI.  (2023)  The protective effect of cyclodextrin on color quality and stability of Cabernet Sauvignon red wine1.  Journal of Integrative Agriculture,      [PMID:16314522]
6. Nan He, Chunxiao Zhang, Kaiyang Hou, Hongxiao Yu, Donghai Zhang, Mengying Chen, Kaiqiang Zhang, Xu Wang.  (2023)  A comprehensive study on flavor/cyclodextrin inclusion complexes.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,  679  (11): (132613).  [PMID:20084102]
7. Qin Jiang, Miao Liu, Luo-Peng Xu, Zi-Ling Lu, Lei Zhang, Lu Zhang.  (2023)  Interfacial Rheological and Emulsion Properties of Self-Assembled Cyclodextrin–Oil Inclusion Complexes.  LANGMUIR,  39  (33): (11675–11683).  [PMID:37551025]
8. Lulu Wang, Yuehai Peng, Wenfang Liu, Li Ren.  (2023)  Properties of Dual-Crosslinked Collagen-Based Membranes as Corneal Repair Material.  Journal of Functional Biomaterials,  14  (7): (360).  [PMID:37504855]
9. Qin Zhang, Fang Guo, Run-Chi Zhao, Zhi-Hong Mo.  (2023)  Toward the green synthesis of CsPbBr3 perovskite nanocrystals using ethanol as an antisolvent and cyclodextrin as a ligand.  NEW JOURNAL OF CHEMISTRY,  47  (20): (9771-9778).  [PMID:]
10. Wanjiao Chen, Weimin Wang, Chuan-Fan Ding, Fangling Wu, Yifeng Mai.  (2023)  Precise analysis of thyroxine enantiomers in pharmaceutical formulation by mobility difference based on cyclodextrin.  Arabian Journal of Chemistry,  16  (104718).  [PMID:]
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12. Fuxing Xu, Shutong Yang, Fangling Wu, Chuan-Fan Ding.  (2023)  Chiral analysis of linear protonated dipeptides by complexing with Cyclodextrins using Ion-Mobility Mass-Spectrometry and DFT structural calculations.  MICROCHEMICAL JOURNAL,  189  (108516).  [PMID:]
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14. Boxuan Yao, Ke Zhang, Xiaoyang Liu, Hua Wei, Zihan Li, Jiarui Zhou, Guangfei Yuan, Xin Wang, Shenghong Yang, Jian Liu.  (2023)  Versatile preparation strategy of negatively charged saccharide-based polymers for selective removal of cationic organic pollutants.  APPLIED SURFACE SCIENCE,  616  (156428).  [PMID:]
15. Yazhen Wu, Xiaoxiao Li, Zhengyu Jin, Birte Svensson, Yuxiang Bai.  (2023)  A practical approach to producing the single-arm linear dextrin, a chimeric glucosaccharide containing an (α-1 → 4) linked portion at the nonreducing end of an (α-1 → 6) glucochain.  CARBOHYDRATE POLYMERS,  305  (120520).  [PMID:36737184]
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17. Lei Jiang, Zeng Liu, Jia Liu, Shu He, Xing Wu, Wei Shao.  (2023)  Supramolecular lignin-containing hydrogel for flexible strain sensor via host-guest interaction and dynamic redox system.  INDUSTRIAL CROPS AND PRODUCTS,  192  (116083).  [PMID:]
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23. Xie Zhen-Hua, Huang Zi-Xin, Zhang Ze-Ping, Rong Min-Zhi, Zhang Ming-Qiu.  (2023)  Imparting Pulley Effect and Self-healability to Cathode Binder of Li-S Battery for Improvement of the Cycling Stability.  CHINESE JOURNAL OF POLYMER SCIENCE,  41  (1): (95-107).  [PMID:]
24. Meixing Wang, Huizhen Hu, Buyu Zhang, Yang Zheng, Pan Wu, Zhenghui Lu, Guimin Zhang.  (2022)  Discovery of a New Microbial Origin Cold-Active Neopullulanase Capable for Effective Conversion of Pullulan to Panose.  INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES,  23  (13): (6928).  [PMID:35805929]
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30. Jianwei Du,Ce Tian,Yajie Liu,Jun Ling,Youxiang Wang.  (2015-04-23)  Azo-capped polysarcosine-b-polylysine as polypeptide gene vector: A new strategy to improve stability and easy optimization via host-guest interaction..  Colloids and surfaces. B, Biointerfaces,  130  (31-39).  [PMID:25899841]
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References

1. You Zhang, Wenzhong Ma, Jing Zhong, Zhou Zhou, Haicun Yang, Zheng Cao, Shuo Wang.  (2024)  Rapid shape recovery and remodeling by tuning the topology of polycaprolactone-based polymer networks.  POLYMER,  292  (126641).  [PMID:]
2. Lin Wang, Fangkun Xiao, Haochen Ge, Yunbo Tong, Congjie Gao, Guiru Zhu.  (2024)  The fabrication of thin-film nanocomposite membrane for organic solvent forward osmosis via host-guest chemistry of α-cyclodextrin.  DESALINATION,  574  (117247).  [PMID:]
3. Hengjun Zhou, Chenyu Liu, Simiao Yu, Farishta Shafiq, Weihong Qiao.  (2024)  Amphiphilic conjugates for solubilization of paclitaxel as efficient drug carriers based on hyaluronic acid and cyclodextrins.  COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS,  683  (133026).  [PMID:]
4. Si-Qi Nie, Yun-Yue Yuan, Hui-Min Zeng, Zhan-Guo Jiang, Cai-Hong Zhan.  (2023)  Homohelical Self-Assembly of Trimer of α-Cyclodextrin and Octamolybdate.  INORGANIC CHEMISTRY,  62  (46): (19153–19158).  [PMID:37934703]
5. Cai-yun LIU, Lu-lu WU, Shu-yue FAN, Yong-sheng TAO, Yun-kui LI.  (2023)  The protective effect of cyclodextrin on color quality and stability of Cabernet Sauvignon red wine1.  Journal of Integrative Agriculture,      [PMID:16314522]
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Solution Calculators