Determine the necessary mass, volume, or concentration for preparing a solution.
| Activity Type | Activity Value -log(M) | Mechanism of Action | Activity Reference | Publications (PubMed IDs) |
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Moligand™, ≥98%(HPLC) Moligand™ for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at -20°C Ships Ice chest + Ice pads 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 2 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
A-485 is a potent and selective catalytic inhibitor of p300/CBP with IC50s of 9.8 nM and 2.6 nM for p300 and CBP histone acetyltransferase (HAT), respectively.
| Pubchem Sid | 504772897 |
|---|---|
| Pubchem Sid Url | https://pubchem.ncbi.nlm.nih.gov/substance/504772897 |
| Canonical Smiles | CNC(NC1=CC=C2C(CC[C@]23C(N(CC(N(CC4=CC=C(F)C=C4)[C@@H](C)C(F)(F)F)=O)C(O3)=O)=O)=C1)=O |
| IUPAC Name | N-[(4-fluorophenyl)methyl]-2-[(3R)-6-(methylcarbamoylamino)-2',4'-dioxospiro[1,2-dihydroindene-3,5'-1,3-oxazolidine]-3'-yl]-N-[(2S)-1,1,1-trifluoropropan-2-yl]acetamide |
| InChIKey | VRVJKILQRBSEAG-LFPIHBKWSA-N |
| INCHI | 1S/C25H24F4N4O5/c1-14(25(27,28)29)32(12-15-3-5-17(26)6-4-15)20(34)13-33-21(35)24(38-23(33)37)10-9-16-11-18(7-8-19(16)24)31-22(36)30-2/h3-8,11,14H,9-10,12-13H2,1-2H3,(H2,30,31,36)/t14-,24+/m0/s1 |
| Isomeric SMILES | C[C@@H](C(F)(F)F)N(CC1=CC=C(C=C1)F)C(=O)CN2C(=O)[C@]3(CCC4=C3C=CC(=C4)NC(=O)NC)OC2=O |
| Molecular Weight | 536.48 |
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 acids and derivatives |
| Class | Carboxylic acids and derivatives |
| Subclass | Amino acids, peptides, and analogues |
| Intermediate Tree Nodes | Amino acids and derivatives |
| Direct Parent | Alpha amino acids and derivatives |
| Alternative Parents | Indanes Oxazolidinediones Fluorobenzenes Aryl fluorides Tertiary carboxylic acid amides Dicarboximides Carbamate esters Ureas Oxacyclic compounds Azacyclic compounds Organopnictogen compounds Organonitrogen compounds Organofluorides Organic oxides Hydrocarbon derivatives Carbonyl compounds Alkyl fluorides |
| Molecular Framework | Aromatic heteropolycyclic compounds |
| Substituents | Alpha-amino acid or derivatives - Indane - Oxazolidinedione - Halobenzene - Fluorobenzene - Benzenoid - Oxazolidinone - Monocyclic benzene moiety - Aryl halide - Aryl fluoride - Carbamic acid ester - Tertiary carboxylic acid amide - Oxazolidine - Dicarboximide - Urea - Carbonic acid derivative - Carboxamide group - Oxacycle - Azacycle - Organoheterocyclic compound - Organic nitrogen compound - Organic oxygen compound - Organopnictogen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Organonitrogen compound - Organofluoride - Organohalogen compound - Carbonyl group - Alkyl halide - Alkyl fluoride - Aromatic heteropolycyclic compound |
| Description | This compound belongs to the class of organic compounds known as alpha amino acids and derivatives. These are amino acids in which the amino group is attached to the carbon atom immediately adjacent to the carboxylate group (alpha carbon), or a derivative thereof. |
| External Descriptors | Not available |
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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 | Apr 03, 2026 | A287597 | |
| Certificate of Analysis | Sep 01, 2025 | A287597 | |
| Certificate of Analysis | Sep 01, 2025 | A287597 | |
| Certificate of Analysis | Sep 01, 2025 | A287597 | |
| Certificate of Analysis | Sep 01, 2025 | A287597 | |
| Certificate of Analysis | Sep 01, 2025 | A287597 | |
| Certificate of Analysis | Sep 01, 2025 | A287597 | |
| Certificate of Analysis | May 21, 2024 | A287597 | |
| Certificate of Analysis | May 21, 2024 | A287597 | |
| Certificate of Analysis | May 21, 2024 | A287597 | |
| Certificate of Analysis | May 21, 2024 | A287597 | |
| Certificate of Analysis | May 21, 2024 | A287597 | |
| Certificate of Analysis | May 21, 2024 | A287597 | |
| Certificate of Analysis | May 21, 2024 | A287597 | |
| Certificate of Analysis | May 21, 2024 | A287597 | |
| Certificate of Analysis | May 21, 2024 | A287597 | |
| Certificate of Analysis | Jun 30, 2022 | A287597 | |
| Certificate of Analysis | Jun 30, 2022 | A287597 | |
| Certificate of Analysis | Jun 30, 2022 | A287597 | |
| Certificate of Analysis | Jun 30, 2022 | A287597 | |
| Certificate of Analysis | Jun 30, 2022 | A287597 | |
| Certificate of Analysis | Jun 30, 2022 | A287597 |
| Solubility | Solvent:DMSO, Max Conc. mg/mL: 53.65, Max Conc. mM: 100; Solvent:ethanol, Max Conc. mg/mL: 53.65, Max Conc. mM: 100 |
|---|---|
| Molecular Weight | 536.500 g/mol |
| XLogP3 | 3.300 |
| Hydrogen Bond Donor Count | 2 |
| Hydrogen Bond Acceptor Count | 9 |
| Rotatable Bond Count | 6 |
| Exact Mass | 536.168 Da |
| Monoisotopic Mass | 536.168 Da |
| Topological Polar Surface Area | 108.000 Ų |
| Heavy Atom Count | 38 |
| Formal Charge | 0 |
| Complexity | 941.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 2 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
| 1. Junhui Lv, Zhinang Yin, Conghui Li, Honglin Wen, Jian Ni, Peiyuan Yang, Zemin Song, Ying Xiang, Honghong Wang, Rui Lu, Li Huang, Ying Zhou, Hai-Bing Zhou, Ruijing Xiao, Pingping Fang, Kaiwei Liang. (2025) KAT6A chimeras form a self-reinforcing epigenetic module with NURF and MLL/COMPASS to sustain AML. GENOME BIOLOGY, [PMID:40830799] [10.1186/s13059-025-03743-y] |
| 2. Zongxin Zhu, Ximiao Chen, Hanwen Zhang, Ronghui Miao, Huiling Yu, Shiying Zhao, Youli Zhang, Tanxin Yu, Di Zhang, Yifei Zhou, Xiaolei Zhang, Wei Zhang. (2026) Lactate-driven H3K27 lactylation promotes Olig2-dependent remyelination and motor recovery after spinal cord injury. NEUROPHARMACOLOGY, [PMID:41525841] [10.1016/j.neuropharm.2026.110832] |
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