Hydroxyecdysone - ≥95%(HPLC), powder , CAS No.5289-74-7

CAS: 5289-74-7 Cat. No.: H108846 Peso molecular: 480.63 Beilstein Registry Number: 1917578 Número EC: 811-097-1
Disponible para pedir
GRADE & PURITY ≥95%(HPLC) powder
Synonyms
HB3718 | BDBM50326777 | LMST01010209 | THE-7 | HY-N6979 | beta-Ecdysone | MLS002207226 | 5-beta-Cholest-7-en-6-one, 2-beta,3-beta,14,20,22,25-hexahydroxy-, (22R)- | 779A7KPL0Y | Bio 101 | HMS2230L09 | s2417 | SCHEMBL22086 | 20-HYDROXYECDYSONE [WHO-DD] | B
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
25mg
H108846-25mg
1
64,90US$
100mg
H108846-100mg
2
125,90US$
500mg
H108846-500mg
2
290,90US$
1g
H108846-1g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
529,90US$
2g
H108846-2g
8-12 wks(?) Production requires sourcing of materials. We appreciate your patience and understanding.
882,90US$
Enter a quantity for the sizes you want to add.
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Why this grade

≥95%(HPLC), powder for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at 2-8°C Ships Wet ice Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 6 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
HB3718 | BDBM50326777 | LMST01010209 | THE-7 | HY-N6979 | beta-Ecdysone | MLS002207226 | 5-beta-Cholest-7-en-6-one, 2-beta, 3-beta, 14, 20, 22, 25-hexahydroxy-, (22R)- | 779A7KPL0Y | Bio 101 | HMS2230L09 | s2417 | SCHEMBL22086 | 20-HYDROXYECDYSONE [WHO-DD] | B
Especificaciones y pureza
≥95%(HPLC), powder
Condiciones de almacenamiento de almacenamiento
Store at 2-8°C
Enviado en
Wet ice
Este producto requiere envío en cadena de frío. Los servicios terrestres y otros servicios económicos no están disponibles.
Pureza
≥95%(HPLC)
Nombres e identificadores
Pubchem Sid504763824
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504763824
Sonrisas canónicasCC12CCC3C(=CC(=O)C4C3(CC(C(C4)O)O)C)C1(CCC2C(C)(C(CCC(C)(C)O)O)O)O
IUPAC Name(2S,3R,5R,9R,10R,13R,14S,17S)-2,3,14-trihydroxy-10,13-dimethyl-17-[(2R,3R)-2,3,6-trihydroxy-6-methylheptan-2-yl]-2,3,4,5,9,11,12,15,16,17-decahydro-1H-cyclopenta[a]phenanthren-6-one
InChIKeyNKDFYOWSKOHCCO-YPVLXUMRSA-N
INCHI1S/C27H44O7/c1-23(2,32)9-8-22(31)26(5,33)21-7-11-27(34)16-12-18(28)17-13-19(29)20(30)14-24(17,3)15(16)6-10-25(21,27)4/h12,15,17,19-22,29-34H,6-11,13-14H2,1-5H3/t15-,17-,19+,20-,21-,22+,24+,25+,26+,27+/m0/s1
Isómeros SMILES C[C@]12CC[C@H]3C(=CC(=O)[C@H]4[C@@]3(C[C@@H]([C@@H](C4)O)O)C)[C@@]1(CC[C@@H]2[C@](C)([C@@H](CCC(C)(C)O)O)O)O
WGK Alemania 2
Peso molecular 480.63
Beilstein 1917578
Reaxy-Rn 2229591
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2229591&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassLipids and lipid-like molecules
ClaseSteroids and steroid derivatives
SubclassBile acids, alcohols and derivatives
Intermediate Tree Nodes Not available
Direct ParentHydroxy bile acids, alcohols and derivatives
Alternative Parents Cholesterols and derivatives  Ecdysteroids  6-oxosteroids  3-hydroxy delta-7-steroids  3-beta-hydroxysteroids  14-hydroxysteroids  Delta-7-steroids  Cyclohexenones  Tertiary alcohols  Secondary alcohols  Cyclic alcohols and derivatives  Polyols  Organic oxides  Hydrocarbon derivatives  
Molecular FrameworkAliphatic homopolycyclic compounds
Substituents Hexahydroxy bile acid, alcohol, or derivatives - Cholesterol - Cholesterol-skeleton - Cholestane-skeleton - Ecdysteroid - 25-hydroxysteroid - Hydroxy bile acid, alcohol, or derivatives - 22-hydroxysteroid - 20-hydroxysteroid - 3-hydroxy-delta-7-steroid - 2-hydroxysteroid - 3-beta-hydroxysteroid - Oxosteroid - 6-oxosteroid - Hydroxysteroid - 3-hydroxysteroid - 14-hydroxysteroid - Delta-7-steroid - Cyclohexenone - Tertiary alcohol - Cyclic alcohol - Secondary alcohol - Ketone - Polyol - Organic oxide - Organic oxygen compound - Hydrocarbon derivative - Carbonyl group - Alcohol - Organooxygen compound - Aliphatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as hydroxy bile acids, alcohols and derivatives. These are bile acids, alcohols or derivatives bearing at least hydroxyl group.
External Descriptors Cholesterol and derivatives
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
ACHE Tclin Acetylcholinesterase (18204 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Tclin Butyrylcholinesterase (7174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CCRF-CEM (65223 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
POLI Tchem DNA polymerase iota (116820 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
EYA2 Tbio Eyes absent homolog 2 (5884 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GMNN Tbio Geminin (128009 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 (2672 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 (2517 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
EcR Ecdysone receptor (102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Abcb1b P-glycoprotein 1 (174 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pseudomonas aeruginosa (123386 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Staphylococcus aureus (210822 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Escherichia coli (133304 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Enterococcus faecalis (29875 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Candida albicans (78123 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Acyrthosiphon pisum (40 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
C2C12 (756 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BCHE Cholinesterase (8742 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Akt1 RAC-alpha serine/threonine-protein kinase (147 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
dengue virus type 2 (2400 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mecanismos de acción
Certificados (CoA, COO, BSE/TSE y tabla de análisis)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

12 results found

Lot NumberCertificate TypeFechaArticulo
C2215199Certificate of AnalysisDec 10, 2025 H108846
C2215226Certificate of AnalysisDec 10, 2025 H108846
K2102050Certificate of AnalysisAug 11, 2025 H108846
I2412050Certificate of AnalysisSep 21, 2024 H108846
H2429099Certificate of AnalysisSep 03, 2024 H108846
I2503127Certificate of AnalysisSep 03, 2024 H108846
D1924074Certificate of AnalysisFeb 06, 2023 H108846
G2227898Certificate of AnalysisJun 12, 2022 H108846
K2327095Certificate of AnalysisJun 12, 2022 H108846
C2215486Certificate of AnalysisMar 01, 2022 H108846
C2215506Certificate of AnalysisMar 01, 2022 H108846
I2412049Certificate of AnalysisMar 01, 2022 H108846

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Propiedades químicas y físicas
Punto de fusión (°C)244°C - 248°C
Peso molecular480.600 g/mol
XLogP30.500
Hydrogen Bond Donor Count6
Hydrogen Bond Acceptor Count7
Rotatable Bond Count5
Exact Mass480.309 Da
Monoisotopic Mass480.309 Da
Topological Polar Surface Area138.000 Ų
Heavy Atom Count34
Formal Charge0
Complexity869.000
Isotope Atom Count0
Defined Atom Stereocenter Count10
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Preguntas frecuentes y artículos
Citations of This Product
Referencias
1. Junyan Wang, Minmin Huang, Haihong Hu, Lushan Yu, Su Zeng.  (2014)  Pregnane X receptor-mediated transcriptional activation of UDP-glucuronosyltransferase 1A1 by natural constituents from foods and herbs.  FOOD CHEMISTRY,      [PMID:24996308] [10.1016/j.foodchem.2014.05.004]
2. Qianqian Huang, Haiying Wu, Xiaoming Qin.  (2023)  Extract of Pfaffia glomerata Ameliorates Paroxetine-Induced Sexual Dysfunction in Male Mice and the Characterization of Its Phytoconstituents by UPLC-MS.  Foods,  12  (17): (3236).  [PMID:37685170] [10.3390/foods12173236]
3. Jia Zeng, Xianchao Shang, Peng Zhang, Hongwei Wang, Yanlong Gu, Jia-Neng Tan.  (2019)  Combined Use of Deep Eutectic Solvents, Macroporous Resins, and Preparative Liquid Chromatography for the Isolation and Purification of Flavonoids and 20-Hydroxyecdysone from Chenopodium quinoa Willd.  Biomolecules,  (12): (776).  [PMID:31775374] [10.3390/biom9120776]
4. Kang He, Huamei Xiao, Yang Sun, Gongming Situ, Yu Xi, Fei Li.  (2019)  microRNA-14 as an efficient suppressor to switch off ecdysone production after ecdysis in insects.  RNA Biology,      [PMID:31184522] [10.1080/15476286.2019.1629768]
5. Ming Liu, Qianwen Wang, Bin Lai, Yan Chen, Rongchumu Ge, Shuo Yan, Chunya Bu.  (2024)  RNA interference targeting β-N-acetylhexosaminidase genes impairs molting and development of Tetranychus urticae.  PESTICIDE BIOCHEMISTRY AND PHYSIOLOGY,      [PMID:40015851] [10.1016/j.pestbp.2024.106259]
6. Wang Guang, Ma Lu, Yang Chen, Du Jianghan, Yang Baocheng, Liu Jingbin, Song Yaole, Sun Xiaoning, Luo Cheng, Sima Yanghu, Xu Shiqing.  (2026)  Habitual dietary alteration reduces egg quality and quantity by affecting ovarian development and nutrient accumulation in Bombyx mori (Lepidoptera: Bombycidae).  JOURNAL OF ECONOMIC ENTOMOLOGY,      [PMID:] [10.1093/jee/toag058]
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