Fmoc-Leu-OH - Moligand™, ≥98% , Agonist of Peroxisome proliferator-activated receptor-γ, CAS No.35661-60-0, Agonist of Peroxisome proliferator-activated receptor-γ

CAS: 35661-60-0 Cat. No.: F100808 Peso molecular: 353.41 Beilstein Registry Number: 2178254 Número EC: 252-662-7
Disponible para pedir
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
Maybridge1_005562 | MFCD00037133 | HMS557E18 | N-(Fluoren-9-ylmethoxycarbonyl)-L-leucine | NSC-334290 | AC-24092 | AKOS010398974 | Fmoc-Leu-OH | Z1123720065 | KF18F70UF3 | N-((9H-FLUOREN-9-YLMETHOXY)CARBONYL)-L-LEUCINE, (-)- | NCGC00255677-01 | BDBM115093
Storage
Store at 2-8°C
Shipped In
Wet ice
 ·  off list, applied to all prices below.
Size
Estado
Price
Qty
5g
F100808-5g
2

9,90US$

14,90US$
Guardar 5,00 US$ (33.56%)
25g
F100808-25g
3

11,90US$

17,90US$
Guardar 6,00 US$ (33.52%)
100g
F100808-100g
3

41,90US$

62,90US$
Guardar 21,00 US$ (33.39%)
500g
F100808-500g
1

156,90US$

235,90US$
Guardar 79,00 US$ (33.49%)
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

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 3 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

Specifications

Sinónimos
Maybridge1_005562 | MFCD00037133 | HMS557E18 | N-(Fluoren-9-ylmethoxycarbonyl)-L-leucine | NSC-334290 | AC-24092 | AKOS010398974 | Fmoc-Leu-OH | Z1123720065 | KF18F70UF3 | N-((9H-FLUOREN-9-YLMETHOXY)CARBONYL)-L-LEUCINE, (-)- | NCGC00255677-01 | BDBM115093
Especificaciones y pureza
Moligand™, ≥98%
Mecanismos bioquímicos y fisiológicos
Anti-inflammatory agent; increases intracellular Ca2+levels.
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.
Grado
Moligand™
Tipo de acción
AGONIST
Mecanismo de acción
Agonist of Peroxisome proliferator-activated receptor-γ
Pureza
≥98%
Nombres e identificadores
Pubchem Sid504760586
Pubchem Sid Urlhttps://pubchem.ncbi.nlm.nih.gov/substance/504760586
Sonrisas canónicasCC(C)CC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
IUPAC Name(2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-4-methylpentanoic acid
InChIKeyCBPJQFCAFFNICX-IBGZPJMESA-N
INCHI1S/C21H23NO4/c1-13(2)11-19(20(23)24)22-21(25)26-12-18-16-9-5-3-7-14(16)15-8-4-6-10-17(15)18/h3-10,13,18-19H,11-12H2,1-2H3,(H,22,25)(H,23,24)/t19-/m0/s1
Isómeros SMILES CC(C)C[C@@H](C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13
WGK Alemania 3
Peso molecular 353.41
Beilstein 2178254
Reaxy-Rn 2307798
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=2307798&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
ClaseCarboxylic acids and derivatives
SubclassAmino acids, peptides, and analogues
Intermediate Tree Nodes Amino acids and derivatives - Alpha amino acids and derivatives
Direct ParentLeucine and derivatives
Alternative Parents Fluorenes  Carbamate esters  Organic carbonic acids and derivatives  Monocarboxylic acids and derivatives  Carboxylic acids  Organopnictogen compounds  Organonitrogen compounds  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homopolycyclic compounds
Substituents Leucine or derivatives - Fluorene - Benzenoid - Carbamic acid ester - Carbonic acid derivative - Carboxylic acid - Monocarboxylic acid or derivatives - Organopnictogen compound - Organooxygen compound - Organonitrogen compound - Organic oxygen compound - Carbonyl group - Organic nitrogen compound - Organic oxide - Hydrocarbon derivative - Aromatic homopolycyclic compound
DescripciónThis compound belongs to the class of organic compounds known as leucine and derivatives. These are compounds containing leucine or a derivative thereof resulting from reaction of leucine at the amino group or the carboxy group, or from the replacement of any hydrogen of glycine by a heteroatom.
External Descriptors Not available
Estructura 3D
Modelo de Estructura Química Interactiva





Objetivos asociados (humanos)
NTSR1 Tchem Neurotensin receptor type 1 (0 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
PPARG Tclin Peroxisome proliferator-activated receptor gamma (1 Activities)
Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)
NR3C1 Tclin Glucocorticoid receptor (14987 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
PPARG Tclin Peroxisome proliferator-activated receptor gamma (15191 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
RXRA Tclin Retinoid X receptor alpha (3637 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
AHR Tclin Aryl hydrocarbon receptor (1071 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GLP1R Tclin Glucagon-like peptide 1 receptor (111429 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
NR1H2 Tchem LXR-beta (3841 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Homo sapiens (32628 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HepG2 (196354 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
BRCA1 Tchem Breast cancer type 1 susceptibility protein (15908 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SNCA Tchem Alpha-synuclein (10960 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SLC36A1 Tchem Proton-coupled amino acid transporter 1 (102 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CTNS Tbio Cystinosin (2 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Objetivos asociados (no humanos)
Ppard Peroxisome proliferator-activated receptor delta (358 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Hdac6 Histone deacetylase 6 (222 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
rep Replicase polyprotein 1ab (378 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nfe2l2 Nuclear factor erythroid 2-related factor 2 (214 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nr1i2 Nuclear receptor subfamily 1 group I member 2 (14 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
SARS-CoV-2 (38078 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.

23 results found

Lot NumberCertificate TypeFechaArticulo
I2215194Certificate of AnalysisJun 15, 2026 F100808
I2215193Certificate of AnalysisJun 15, 2026 F100808
I2215179Certificate of AnalysisJun 15, 2026 F100808
I2215178Certificate of AnalysisJun 15, 2026 F100808
K2513299Certificate of AnalysisNov 03, 2025 F100808
K2513298Certificate of AnalysisNov 03, 2025 F100808
K2513297Certificate of AnalysisNov 03, 2025 F100808
K2513296Certificate of AnalysisNov 03, 2025 F100808
H2512589Certificate of AnalysisApr 09, 2025 F100808
J2514796Certificate of AnalysisApr 09, 2025 F100808
H2512597Certificate of AnalysisApr 09, 2025 F100808
H2504273Certificate of AnalysisApr 09, 2025 F100808
H2504270Certificate of AnalysisApr 09, 2025 F100808
H2124387Certificate of AnalysisApr 02, 2025 F100808
H2124226Certificate of AnalysisApr 02, 2025 F100808
H2124221Certificate of AnalysisApr 02, 2025 F100808
H2124220Certificate of AnalysisApr 02, 2025 F100808
E2515324Certificate of AnalysisJul 11, 2024 F100808
E2515323Certificate of AnalysisJul 11, 2024 F100808
E2515305Certificate of AnalysisJul 11, 2024 F100808
C1912133Certificate of AnalysisDec 14, 2022 F100808
H2401033Certificate of AnalysisJun 16, 2022 F100808
I2423655Certificate of AnalysisJun 19, 2021 F100808

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Propiedades químicas y físicas
SolubilidadSolvent:DMSO, Max Conc. mg/mL: 35.34, Max Conc. mM: 100 with gentle warming
Rotación específica [α]-25 ° (C=1, DMF)
Punto de fusión (°C)153-157°C
Peso molecular353.400 g/mol
XLogP34.400
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count4
Rotatable Bond Count7
Exact Mass353.163 Da
Monoisotopic Mass353.163 Da
Topological Polar Surface Area75.600 Ų
Heavy Atom Count26
Formal Charge0
Complexity484.000
Isotope Atom Count0
Defined Atom Stereocenter Count1
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. Jianchao Zhang, Caibing Ma, Yongjun Yu, Chaowei Liu, Lijing Fang, Hai Rao.  (2023)  Single amino acid-based PROTACs trigger degradation of the oncogenic kinase BCR-ABL in chronic myeloid leukemia (CML).  JOURNAL OF BIOLOGICAL CHEMISTRY,      [PMID:37392851] [10.1016/j.jbc.2023.104994]
2. Xianlin Xu, Guodong Zhao, Hang Wang, Xiaojie Li, Xi Feng, Bowen Cheng, Lei Shi, Weimin Kang, Xupin Zhuang, Yan Yin.  (2018)  Bio-inspired amino-acid-functionalized cellulose whiskers incorporated into sulfonated polysulfone for proton exchange membrane.  JOURNAL OF POWER SOURCES,      [PMID:] [10.1016/j.jpowsour.2018.11.003]
3. Like Lin, Cong Li, Yujiao Zhang, Li Zhang, Lu Gao, Lihua Jin, Yu Shu, Yehua Shen.  (2024)  Effect of Akt-activating peptide obtained from walnut protein degradation on the prevention of memory impairment in mice.  Food & Function,      [PMID:38305469] [10.1039/D3FO04479C]
Calculadoras de soluciones
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