Alendronic Acid - Moligand™, ≥98% , Inhibitor of farnesyl diphosphate synthase, CAS No.66376-36-1, Inhibitor of farnesyl diphosphate synthase

CAS: 66376-36-1 Cat. No.: A136993 Summenformel: C4H13NO7P2 Molekulargewicht: 249.1 EG-Nummer: 689-696-0
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GRADE & PURITY Moligand™ ? Moligand™ — Aladdin's line of ligands and bioactive small molecules. Use for receptor, pathway, and binding studies needing defined small-molecule tools. ≥98%
Synonyms
(4-amino-1-hydroxy-1-phosphonobutyl)phosphonic acid | (4-amino-1-hydroxy-1-phosphono-butyl)phosphonic acid | Acido alendronico [INN-Spanish] | ALENDRONATE (MART.) | 1yhm | Q420057 | alpha-hydroxy-delta-aminobutylidenediphosphonic acid | BPH 1 | 4-Amino-1-
Storage
Protected from light,Room temperature
Shipped In
Normal
★
Size
Deutschland (EU)
USA*
Price
Qty
1g
A136993-1g
—
Auf Lager ≥10

12,93€

19,87€
Speichern 6,94 € (34.93%)
5g
A136993-5g
—
Auf Lager ≥10

46,77€

70,20€
Speichern 23,43 € (33.37%)
25g
A136993-25g
—
7 Auf Lager

104,04€

156,11€
Speichern 52,06 € (33.35%)
Enter a quantity for the sizes you want to add.
🧪

Why this grade

Moligand™, ≥98% Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Protected from light,Room temperature Ships Normal 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 20 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Übersicht

Alendronate acid is an inhibitor of FDPS. It is a bisphosphonate that inhibits osteoclast-mediated bone resorption. Unlike pyrophosphate, the endogenous regulator of bone turnover to which it is chemically related, alendronate specifically inhibits osteoclastic osteoclastic bone resorption, having no effect on mineralization of bone newly formed by osteoblasts.
An inhibitor of FDPS

Specifications

Synonyme
(4-amino-1-hydroxy-1-phosphonobutyl)phosphonic acid | (4-amino-1-hydroxy-1-phosphono-butyl)phosphonic acid | Acido alendronico [INN-Spanish] | ALENDRONATE (MART.) | 1yhm | Q420057 | alpha-hydroxy-delta-aminobutylidenediphosphonic acid | BPH 1 | 4-Amino-1-
Spezifikationen & Reinheit
Moligand™, ≥98%
Storage
Protected from light,Room temperature
Verschickt in
Normal
Note
Moligand™
Aktionsart
INHIBITOR
Mechanismus der Wirkung
Inhibitor of farnesyl diphosphate synthase
Reinheit
≥98%
Namen und Kennungen
Pubchem Sid488179658
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/488179658
Kanonisches LächelnC(CC(O)(P(=O)(O)O)P(=O)(O)O)CN
IUPAC Name(4-amino-1-hydroxy-1-phosphonobutyl)phosphonic acid
InChIKeyOGSPWJRAVKPPFI-UHFFFAOYSA-N
INCHI1S/C4H13NO7P2/c5-3-1-2-4(6,13(7,8)9)14(10,11)12/h6H,1-3,5H2,(H2,7,8,9)(H2,10,11,12)
Isomere SMILES C(CC(O)(P(=O)(O)O)P(=O)(O)O)CN
RTECS SZ6521833
Alternative CAS-Nummer 121268-17-5
Molekulargewicht 249.1
Reaxy-Rn 2275403
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2275403&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
SuperclassOrganic acids and derivatives
KlasseOrganic phosphonic acids and derivatives
SubclassBisphosphonates
Intermediate Tree Nodes Not available
Direct ParentBisphosphonates
Alternative Parents Organic phosphonic acids  Organopnictogen compounds  Organophosphorus compounds  Organooxygen compounds  Organic oxides  Monoalkylamines  Hydrocarbon derivatives  
Molecular FrameworkAliphatic acyclic compounds
Substituents Bisphosphonate - Organophosphonic acid - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Primary amine - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Primary aliphatic amine - Amine - Aliphatic acyclic compound
BeschreibungThis compound belongs to the class of organic compounds known as bisphosphonates. These are organic compounds containing two phosphonate groups linked together through a carbon atoms.
External Descriptors primary amino compound - 1,1-bis(phosphonic acid)
3D-Struktur
Interaktives chemisches Strukturmodell





Zugehörige Ziele (menschlich)
FDPS Tclin Farnesyl pyrophosphate synthase (10 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
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
F2 Tclin Thrombin (11687 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
FDPS Tclin Farnesyl diphosphate synthase (1240 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
DRD2 Tclin Dopamine D2 receptor (23596 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GABRA1 Tclin GABA receptor alpha-1 subunit (399 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
AVPR2 Tclin Vasopressin V2 receptor (2912 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
ADORA1 Tclin Adenosine A1 receptor (17603 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AGTR1 Tclin Type-1 angiotensin II receptor (5176 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
CRHR1 Tclin Corticotropin releasing factor receptor 1 (2996 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
HTR3A Tclin Serotonin 3a (5-HT3a) receptor (3366 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GCGR Tclin Glucagon receptor (2563 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Zugehörige Ziele (nicht menschlich)
Htr7 Serotonin 7 (5-HT7) receptor (19 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
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
Ntsr1 Neurotensin receptor 1 (48 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Pde4d Phosphodiesterase 4D (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Bdkrb1 Bradykinin B1 receptor (77 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
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Ptpn1 Protein-tyrosine phosphatase 1B (270 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mmp9 Matrix metalloproteinase 9 (38 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trypanosoma brucei (78846 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Entamoeba histolytica (2676 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Plasmodium falciparum (966862 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Leishmania donovani (89745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Trypanosoma cruzi (99888 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Toxoplasma gondii (4585 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Mus musculus (284745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Rattus norvegicus (775804 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Dictyostelium discoideum (81 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
J774.A1 (2436 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RAW264.7 (28094 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Farnesyl pyrophosphate synthase (85 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Glra2 Glycine receptor (1745 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
MC3T3-E1 (421 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Wirkungsmechanismen
Zertifikate (CoA, COO, BSE/TSE und Analyse-Diagramm)
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.

22 results found

Lot NumberCertificate TypeDatumArtikel
H2205713Certificate of AnalysisMar 11, 2026 A136993
H2205712Certificate of AnalysisMar 11, 2026 A136993
F2513194Certificate of AnalysisJun 24, 2025 A136993
F2513195Certificate of AnalysisJun 24, 2025 A136993
F2513197Certificate of AnalysisJun 24, 2025 A136993
I2311168Certificate of AnalysisJul 19, 2023 A136993
I2311150Certificate of AnalysisJul 19, 2023 A136993
I2311149Certificate of AnalysisJul 19, 2023 A136993
G2320308Certificate of AnalysisJun 05, 2023 A136993
G2320303Certificate of AnalysisJun 05, 2023 A136993
G2320304Certificate of AnalysisJun 05, 2023 A136993
G2320305Certificate of AnalysisJun 05, 2023 A136993
G2320307Certificate of AnalysisJun 05, 2023 A136993
J2010113Certificate of AnalysisAug 11, 2022 A136993
G2220411Certificate of AnalysisJul 25, 2022 A136993
E2315393Certificate of AnalysisJul 25, 2022 A136993
H2205714Certificate of AnalysisJul 25, 2022 A136993
D2310190Certificate of AnalysisJul 25, 2022 A136993
E2315384Certificate of AnalysisJul 25, 2022 A136993
A2211273Certificate of AnalysisJan 05, 2022 A136993
A2211272Certificate of AnalysisJan 05, 2022 A136993
A2211264Certificate of AnalysisJan 05, 2022 A136993

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Chemische und physikalische Eigenschaften
EmpfindlichkeitLight sensitive
Schmelzpunkt (°C)235°C(dec.)(lit.)
Molekulargewicht249.100 g/mol
XLogP3-6.500
Hydrogen Bond Donor Count6
Hydrogen Bond Acceptor Count8
Rotatable Bond Count5
Exact Mass249.017 Da
Monoisotopic Mass249.017 Da
Topological Polar Surface Area161.000 Ų
Heavy Atom Count14
Formal Charge0
Complexity257.000
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
The total count of all stereochemical bonds0
Covalently-Bonded Unit Count1
Citations of This Product
Referenzen
1. Wentao Shi, Yan Gao, Yiqing Wu, Jiaqi Sun, Bai Xu, Xiaojie Lu, Qing Wang.  (2023)  A multifunctional polydopamine/genipin/alendronate nanoparticle licences fibrin hydrogels osteoinductive and immunomodulatory potencies for repairing bone defects.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:37524274] [10.1016/j.ijbiomac.2023.126072]
2. Yan Huang, Maowen Chen, Yiding Shen, Xinkun Shen, Menghuan Li, Yanan Li, Yuan Liu, Kaiyong Cai, Zhong Luo, Yan Hu.  (2023)  Bone-targeting cell membrane-engineered CaCO3-based nanoparticles restore local bone homeostasis for microenvironment-responsive osteoporosis treatment.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2023.144145]
3. Yonghui Wu, Lu Yang, Qianqian Wu, Qingshan Liu, Ling Zou, Xiaochao Yang, Keyong Tang.  (2023)  Regulation of the Oxidase Mimetic Activity of Ceria Nanoparticles by Buffer Composition.  CHEMISTRY-A EUROPEAN JOURNAL,  29  (29): (e202204071).  [PMID:36879435] [10.1002/chem.202204071]
4. Yimin Niu, Hongbin Yang, Zhenyan Yu, Cuicui Gao, Shuaishuai Ji, Jie Yan, Lei Han, Qiang Huo, Ming Xu, Yang Liu.  (2022)  Intervention with the Bone-Associated Tumor Vicious Cycle through Dual-Protein Therapeutics for Treatment of Skeletal-Related Events and Bone Metastases.  ACS Nano,      [PMID:35077154] [10.1021/acsnano.1c08269]
5. Shan Zhang, Ruiqi Liang, Kun Xu, Shurong Zheng, Somnath Mukherjee, Peng Liu, Changhao Wang, Yashao Chen.  (2021)  Construction of multifunctional micro-patterned PALNMA/PDADMAC/PEGDA hydrogel and intelligently responsive antibacterial coating HA/BBR on Mg alloy surface for orthopedic application.  Materials Science & Engineering C-Materials for Biological Applications,      [PMID:35148866] [10.1016/j.msec.2021.112636]
6. Zhenyu Zhao, Gen Li, Huitong Ruan, Keyi Chen, Zhengwei Cai, Guanghua Lu, Runmin Li, Lianfu Deng, Ming Cai, Wenguo Cui.  (2021)  Capturing Magnesium Ions via Microfluidic Hydrogel Microspheres for Promoting Cancellous Bone Regeneration.  ACS Nano,      [PMID:34342981] [10.1021/acsnano.1c02147]
7. Lei Chen, Yufei Tang, Kang Zhao, Xiang Zha, Min Wei, Quanchang Tan, Zixiang Wu.  (2020)  Sequential release of double drug (graded distribution) loaded gelatin microspheres/PMMA bone cement.  Journal of Materials Chemistry B,  9  (2): (508-522).  [PMID:33305784] [10.1039/D0TB01452D]
8. Xiaonan Zhang, Kang Chen, Bo Wei, Xingwang Liu, Zeming Lei, Xizhuang Bai.  (2016)  Ginsenosides Rg3 attenuates glucocorticoid-induced osteoporosis through regulating BMP-2/BMPR1A/Runx2 signaling pathway.  CHEMICO-BIOLOGICAL INTERACTIONS,      [PMID:27387537] [10.1016/j.cbi.2016.07.003]
9. Hong Gao, Chen Wang, Wenqi Zhang, Guowei Shan, Weixing Li.  (2025)  Alendronic acid/Cu-MOF-74 nanorods arrayed interlayer regulated nanofiltration membrane to separate glutathione from amino acids.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2025.132291]
10. Yu Chen, Qi-Wen Chen, Fang-Sheng Fu, Hui-Yun Gu, Aixi Yu, Xian-Zheng Zhang.  (2024)  Bone Destruction-Chemotactic Osteoprogenitor Cells Deliver Liposome Nanomedicines for the Treatment of Osteosarcoma and Osteoporosis.  ACS Nano,      [PMID:39424791] [10.1021/acsnano.4c10053]
11. Han Lu, Song Yaqi, Chen Min, Pan Leiqing, Tu Kang, Su Jing.  (2025)  Development of a PCR fluorescence sensor utilizing an upconversion FRET system for rapid and ultra-sensitive determination of Escherichia coli.  MICROCHIMICA ACTA,  192  (4): (1-11).  [PMID:40053209] [10.1007/s00604-025-07077-1]
12. Wu-Shang Yang, Ze-Lin Qiu, Wen-Han Yu, Li-Feng Fang, Bao-Ku Zhu.  (2024)  Integrating binary organic phosphonic acid into nanofiltration membrane for high precision separation of mono-/divalent anions.  SEPARATION AND PURIFICATION TECHNOLOGY,      [PMID:] [10.1016/j.seppur.2024.126287]
13. Chunting He, Penghui He, Yangsen Ou, Xue Tang, Hongjiao Wei, Yanhua Xu, Shuting Bai, Zhaofei Guo, Rui Hu, Kun Xiong, Guangsheng Du, Xun Sun.  (2025)  Rectifying the Crosstalk between the Skeletal and Immune Systems Improves Osteoporosis Treatment by Core–Shell Nanocapsules.  ACS Nano,      [PMID:39879106] [10.1021/acsnano.4c14728]
14. Wenhui Wang, Xinyu Zeng, Zhiliang Gao, Linqiang Mei, Chang Pan, Jie Li, Yuguo Chen.  (2025)  A polymer-based “immunogenic cell death” amplifier promotes systemic breast cancer inhibition through combined mitochondrial oxidative stress and calcium overload.  CHEMICAL ENGINEERING JOURNAL,      [PMID:] [10.1016/j.cej.2025.165725]
15. Yayu Wang, Jie Yao, Lizhao Cai, Tong Liu, Xiaogang Wang, Ye Zhang, Zhiying Zhou, Tingwei Li, Minyi Liu, Renfa Lai, Xiangning Liu.  (2023)  Bone-Targeted Extracellular Vesicles from Mesenchymal Stem Cells for Osteoporosis Therapy.  International Journal of Nanomedicine,      [PMID:33116512] [10.2147/IJN.S263756]
16. Pei-Jie Zhang, Dong Zhou, Zi-Wei Yang, Yong-Guo Hu, Meng-Wen Ma, Jin-Xuan Fan, Yuan-Di Zhao, Jia-Hua Zou.  (2025)  Salmonella-Derived Fluorescent Carbon Dots for Reprogramming Tumor-Associated Macrophages and Enhancing Tumor Photodynamic Therapy.  ACS Applied Bio Materials,      [PMID:40411829] [10.1021/acsabm.5c00624]
17. Xiaoming Li, Shuang Yang, Shidan Li, Pengfei Wu, Wenhui Hu, Wei Dai, Jingru Xie, Jinlong Qiu, Liang Zhang, Hui Zhao, Shiwu Dong.  (2025)  Reverse biogradient biomimetic periosteum with osteogenic and angiogenic characteristics for bone regeneration.  Materials Today Bio,      [PMID:40585030] [10.1016/j.mtbio.2025.101967]
18. Xuanzuo JIANG, Feifei Feng, Wenyuan JIA, Yuheng YANG, Yongzheng YAN, Zhiqiang CHENG, Yungang LUO, Ji QU, Guomin LIU.  (2025)  Treatment of osteoporotic bone defects with carboxymethyl chitosan based biomimetic mineralized hydrogel loaded with icaritin.  INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES,      [PMID:41260430] [10.1016/j.ijbiomac.2025.149089]
19. Yiyi Yu, Xin Sun, Xiaokun Yue, Huyue Zhang, Shuo Chen, Guang Yang, Qian Luo, Chuanglong He, Xiaojun Zhou.  (2026)  Programmed regulation of microenvironment remodeling and bone regeneration for bone repair by coaxial hydrogel scaffold with ultrasound-activated drug delivery.  Materials Today Bio,      [PMID:41852876] [10.1016/j.mtbio.2026.102988]
20. Chen Wang, Chenxuan Shao, Houyi Peng, Yanchen Liu, Qi Zhang, Xiaohui Ju, Weixing Li.  (2026)  Surface charge-regulated nanofiltration membrane for precise separation cordycepin from salts.  JOURNAL OF MEMBRANE SCIENCE,      [PMID:] [10.1016/j.memsci.2026.126068]
Lösungsrechner
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Häufig gestellte Fragen

What is the purity of this product?
This product is supplied at ≥98% purity (chemical assay). Lot-specific values are stated on the Certificate of Analysis.
What is Moligand??
Moligand? is one of Aladdin Scientific's premium product lines, formulated for high-purity applications across multiple workflows. Compared to standard grades in the same workflow, Moligand? products typically offer tighter specifications, more rigorous QC, and stronger lot-to-lot consistency.
How should this product be stored?
Store at room temperature, protected from light. The material is light-sensitive — keep it in its original opaque or amber container.
How is this product shipped?
This product ships under standard ambient conditions. No temperature-controlled packaging is required.
What are the CAS number, molecular formula and molecular weight?
The CAS Number is 66376-36-1, the molecular formula is C4H13NO7P2, and the molecular weight is 249.1 g/mol. InChIKey OGSPWJRAVKPPFI-UHFFFAOYSA-N.
What documentation is provided?
Available product documentation, including Certificates of Analysis (COA), Safety Data Sheets (SDS), and specification sheets, is shown in the product document area. Document availability and access follow the current site policy.

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