Determine the necessary mass, volume, or concentration for preparing a solution.
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≥80%, 750 μg/mg for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 22 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
| Canonical Smiles | CC1C=CC=CC=CC=CC=CC=CC=CC(CC2C(C(CC(O2)(CC(CC(C(CCC(CC(CC(=O)OC(C(C1O)C)C)O)O)O)O)O)O)O)C(=O)O)OC3C(C(C(C(O3)C)O)N)O |
|---|---|
| IUPAC Name | (1R,3S,5R,6R,9R,11R,15S,16R,17R,18S,19E,21E,23E,25E,27E,29E,31E,33R,35S,36R,37S)-33-[(2R,3S,4S,5S,6R)-4-amino-3,5-dihydroxy-6-methyloxan-2-yl]oxy-1,3,5,6,9,11,17,37-octahydroxy-15,16,18-trimethyl-13-oxo-14,39-dioxabicyclo[33.3.1]nonatriaconta-19,21,23,25,27,29,31-heptaene-36-carboxylic acid |
| InChIKey | APKFDSVGJQXUKY-INPOYWNPSA-N |
| INCHI | 1S/C47H73NO17/c1-27-17-15-13-11-9-7-5-6-8-10-12-14-16-18-34(64-46-44(58)41(48)43(57)30(4)63-46)24-38-40(45(59)60)37(54)26-47(61,65-38)25-33(51)22-36(53)35(52)20-19-31(49)21-32(50)23-39(55)62-29(3)28(2)42(27)56/h5-18,27-38,40-44,46,49-54,56-58,61H,19-26,48H2,1-4H3,(H,59,60)/b6-5+,9-7+,10-8+,13-11+,14-12+,17-15+,18-16+/t27-,28-,29-,30+,31+,32+,33-,34-,35+,36+,37-,38-,40+,41-,42+,43+,44-,46-,47+/m0/s1 |
| Isomeric SMILES | C[C@H]1/C=C/C=C/C=C/C=C/C=C/C=C/C=C/[C@@H](C[C@H]2[C@@H]([C@H](C[C@](O2)(C[C@H](C[C@H]([C@@H](CC[C@H](C[C@H](CC(=O)O[C@H]([C@@H]([C@@H]1O)C)C)O)O)O)O)O)O)O)C(=O)O)O[C@H]3[C@H]([C@H]([C@@H]([C@H](O3)C)O)N)O |
| Alternate CAS | 1202017-46-6 |
| Molecular Weight | 924.08 |
| Beilstein | 78342 |
| Reaxy-Rn | 31131291 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=31131291&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organic oxygen compounds |
| Class | Organooxygen compounds |
| Subclass | Carbohydrates and carbohydrate conjugates |
| Intermediate Tree Nodes | Aminosaccharides |
| Direct Parent | Aminoglycosides |
| Alternative Parents | Macrolides and analogues Hexoses O-glycosyl compounds Beta hydroxy acids and derivatives Oxanes Dicarboxylic acids and derivatives Secondary alcohols 1,2-aminoalcohols Amino acids Lactones Hemiacetals Carboxylic acid esters Polyols Oxacyclic compounds Acetals Carboxylic acids Carbonyl compounds Hydrocarbon derivatives Monoalkylamines Organic oxides Organopnictogen compounds |
| Molecular Framework | Aliphatic heteropolycyclic compounds |
| Substituents | Aminoglycoside core - Macrolide - Hexose monosaccharide - O-glycosyl compound - Glycosyl compound - Beta-hydroxy acid - Dicarboxylic acid or derivatives - Oxane - Hydroxy acid - Monosaccharide - 1,2-aminoalcohol - Hemiacetal - Secondary alcohol - Lactone - Carboxylic acid ester - Amino acid or derivatives - Amino acid - Carboxylic acid derivative - Polyol - Organoheterocyclic compound - Oxacycle - Acetal - Carboxylic acid - Organic nitrogen compound - Primary aliphatic amine - Organonitrogen compound - Carbonyl group - Primary amine - Hydrocarbon derivative - Organic oxide - Amine - Alcohol - Organopnictogen compound - Aliphatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as aminoglycosides. These are molecules or a portion of a molecule composed of amino-modified sugars. |
| External Descriptors | Polyenes |
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Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Date | Item |
|---|---|---|---|
| Certificate of Analysis | Nov 28, 2025 | A105482 | |
| Certificate of Analysis | Jun 17, 2025 | A105482 | |
| Certificate of Analysis | Dec 17, 2024 | A105482 | |
| Certificate of Analysis | Mar 11, 2024 | A105482 | |
| Certificate of Analysis | Nov 08, 2023 | A105482 | |
| Certificate of Analysis | Nov 08, 2023 | A105482 | |
| Certificate of Analysis | Nov 06, 2023 | A105482 | |
| Certificate of Analysis | Mar 26, 2021 | A105482 | |
| Certificate of Analysis | Mar 26, 2021 | A105482 | |
| Certificate of Analysis | Mar 26, 2021 | A105482 | |
| Certificate of Analysis | Mar 26, 2021 | A105482 |
| Solubility | Soluble in aqueous buffers at pH 2.0 or 11.0. Insoluble at pH 6.0-7.0. Also soluble in DMSO or DMF |
|---|---|
| Sensitivity | Light & Moisture sensitive |
| Melt Point(°C) | >170°C |
| Molecular Weight | 924.100 g/mol |
| XLogP3 | 0.000 |
| Hydrogen Bond Donor Count | 12 |
| Hydrogen Bond Acceptor Count | 18 |
| Rotatable Bond Count | 3 |
| Exact Mass | 923.488 Da |
| Monoisotopic Mass | 923.488 Da |
| Topological Polar Surface Area | 320.000 Ų |
| Heavy Atom Count | 65 |
| Formal Charge | 0 |
| Complexity | 1670.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 19 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 7 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 7 |
| Covalently-Bonded Unit Count | 1 |
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| 2. Haifeng Lu, Qi Lu, Hongwu Sun, Zhongkun Wang, Xiang Shi, Yuling Ding, Xiang Ran, Jing Pei, Yubo Pan, Qunlin Zhang. (2023) ROS-Responsive Fluorescent Sensor Array for Precise Diagnosis of Cancer via pH-Controlled Multicolor Gold Nanoclusters. ACS Applied Materials & Interfaces, [PMID:37531495] [10.1021/acsami.3c09320] |
| 3. Mingzhu Zhu, Chen He, Jinchuan Zhou, Yi Li, Lilin Qian, Jiaozhen Zhang, Yanan Qiao, Wenqiang Chang, Hongxiang Lou. (2023) Liverwort-Derived Metabolites Retard Endophyte Growth and Inspire Antifungal Application. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, [PMID:36919252] [10.1021/acs.jafc.2c08866] |
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| 5. Guo Penghao, Chen Jianlong, Tan Yiwei, Xia Li, Zhang Weizheng, Li Xiaojie, Jiang Yujie, Li Ruiying, Chen Chunmei, Liao Kang, Peng Yaqin. (2022) Comparison of molecular and MALDI-TOF MS identification and antifungal susceptibility of clinical Fusarium isolates in Southern China. Frontiers in Microbiology, [PMID:36386677] [10.3389/fmicb.2022.992582] |
| 6. Xinhua Liu, Youteng Qin, Liyun Dong, Ziyi Han, Tianning Liu, Ying Tang, Yun Yu, Jingjie Ye, Juan Tao, Xuan Zeng, Jun Feng, Xian-Zheng Zhang. (2022) Living symbiotic bacteria-involved skin dressing to combat indigenous pathogens for microbiome-based biotherapy toward atopic dermatitis. Bioactive Materials, [PMID:36157249] [10.1016/j.bioactmat.2022.08.019] |
| 7. Zhongjia Yu, Xiang-Fang Yu, Goher Kerem, Pei-Gen Ren. (2022) Perturbation on gut microbiota impedes the onset of obesity in high fat diet-induced mice. Frontiers in Endocrinology, [PMID:36017311] [10.3389/fendo.2022.795371] |
| 8. Xin Yang, Zejun Pei, Renjing Hu, Zhehao Zhang, Zaixiang Lou, Xin Sun. (2021) Study on the Inhibitory Activity and Possible Mechanism of Myriocin on Clinically Relevant Drug-Resistant Candida albicans and Its Biofilms. BIOLOGICAL & PHARMACEUTICAL BULLETIN, 44 (3): (305-315). [PMID:33441497] [10.1248/bpb.b20-00246] |
| 9. Xiaowen He, Lantong Zhang, Jinping Chen, Jinlei Sui, Guohui Yi, Jinyan Wu, Yinzheng Ma. (2019) Correlation between Chemical Composition and Antifungal Activity of Clausena lansium Essential Oil against Candida spp.. MOLECULES, 24 (7): (1394). [PMID:30970599] [10.3390/molecules24071394] |
| 10. Chen Xing, Chunqing Qin, Xueqing Li, Fuming Zhang, Robert J. Linhardt, Peilong Sun, Anqiang Zhang. (2019) Chemical composition and biological activities of essential oil isolated by HS-SPME and UAHD from fruits of bergamot. LWT-FOOD SCIENCE AND TECHNOLOGY, [PMID:] [10.1016/j.lwt.2019.01.020] |
| 11. Lu Wang, Yanan Wu, Tao Huang, Kan Shi, Zhenqiang Wu. (2017) Chemical Compositions, Antioxidant and Antimicrobial Activities of Essential Oils of Psidium guajava L. Leaves from Different Geographic Regions in China. CHEMISTRY & BIODIVERSITY, 14 (9): (e1700114). [PMID:28618209] [10.1002/cbdv.201700114] |
| 12. Wang Aoke, Ahmad Aftab, Ullah Sadeeq, Cheng Li, Ke Lin, Yuan Qipeng. (2017) A Cheap and Convenient Method of Liposome Preparation Using Glass Beads as a Source of Shear Force. AAPS PHARMSCITECH, 18 (8): (3227-3235). [PMID:28560505] [10.1208/s12249-017-0812-3] |
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| 14. Gao Mei-yue, Qi Huan, Li Jian-song, Zhang Hui, Zhang Ji, Wang Ji-dong, Xiang Wen-sheng. (2016) A new polysubstituted cyclopentene derivative from Streptomyces sp. HS-NF-1046. JOURNAL OF ANTIBIOTICS, 70 (2): (216-218). [PMID:27599764] [10.1038/ja.2016.111] |
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| 17. Li Wanqian, Whiteway Malcolm, Hang Sijin, Yu Jinhua, Lu Hui, Jiang Yuanying. (2025) Impairing the interaction between Erg11 and cytochrome P450 reductase Ncp1 enhances azoles’ antifungal activities. Nature Communications, 16 (1): (1-18). [PMID:40707518] [10.1038/s41467-025-62131-z] |
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