Aceclofenac - ≥98%(HPLC) , Cyclooxygenase-2 inhibitor, CAS No.89796-99-6, Cyclooxygenase-2 inhibitor

CAS: 89796-99-6 Cat. No.: A151117 Formule: C16H13Cl2NO4 Poids moléculaire: 354.18 Numéro CE: 641-844-5
DISPONIBLE À COMMANDE
QUALITÉ & PURETÉ ≥98%(HPLC)
Synonyms
2-((2,6-Dichlorophenyl)amino)benzeneacetic acid carboxymethyl ester|ClanzaCR|Cincofen|Hifenac|ACECLOFENAC [MI]|Acide picrique|Aceclofenac|Aceclofenac (TN)|Aceclofenac for peak identification|2-[(2',6'-dichlorophenyl)amino]phenylacetoxyacetic acid|2-[(2,6-dichlorophenyl)amino]phenylacetoxyacetic acid|[({2-[(2,6-dichlorophenyl)amino]phenyl}acetyl)oxy]acetic acid|Aceclofenac [INN:BAN]|ACECLOFENAC [MART.]|4-Methyl-6-nitroaniline|Benzeneacetic acid, 2-[(2,6-dichlorophenyl)amino]-, carboxymethyl ester|Aceclofenac-d4,13C2(major)|ACECLOFENAC [WHO-DD]|2-[(2,6-dichlorophenyl)amino]benzeneacetic acid carboxymethyl ester|Aceclofenac (JAN/INN)|o-Carbamoylbenzoic acid|ACECLOFENAC (EP MONOGRAPH)|p-Xylene, 2-nitro-|Aceclofenacum|2-[2-(2,6-Dichloroanilino)phenylacetoxy]acetic Acid|ACECLOFENAC BETADEX [WHO-DD]|ACECLOFENAC [JAN]|Dinitrobenzenesulfonic acid|o-Phthalic acid diamide|2-(o-(2,6-Dichloranilino)phenylacetoxy)essigsaeure|o-Acetoaminobenozic acid|5-nitro-2,3-dihydro-1H-isoindole-1,3-dione|2-({2-[2-(2,6-DICHLOROANILINO)PHENYL]ACETYL}OXY)ACETIC ACID|Clanza|2-(2-(2-(2,6-dichlorophenylamino)phenyl)acetoxy)acetic acid|1H,3H-Benzo[1,2-c:4,5-c']difuran-1,3,5,7-tetrone|Aceclofenacum (Latin)|Airtal|Glycolic acid, (o-(2,6-dichloroanilino)phenyl)acetate (ester)|ACECLOFENAC [INN]|Aceclofenaco [Spanish]|2-(2-(2-((2,6-dichlorophenyl)amino)phenyl)acetoxy)acetic acid|Benzene, 2,5-dichloronitro-|Glycolic acid (o-(2,6-dichloroanilino)phenyl)acetate|Glycolic Acid [o-(2,6-Dichloroanilino)phenyl]acetate Ester|(2-{2-[(2,6-dichlorophenyl)amino]phenyl}acetoxy)acetic acid|ACECLOFENAC (MART.)|2-[2-[2-(2,6-dichloroanilino)phenyl]acetyl]oxyacetic acid|Benzeneacetic acid, 2-((2,6-dichlorophenyl)amino)-, carboxymethyl ester|Toluene, 4-chloro-2-nitro-|2-(2,6-dichlorophenylamine)phenylacetoxyacetic acid|Phthalyl dichloride|Preservex|2-((2',6'-dichlorophenyl)amino)phenylacetoxyacetic acid|2-((2,6-dichlorophenyl)amino)phenylacetoxyacetic acid|Aceclofenac betadex|Aceclofenaco
Storage
Room temperature
Shipped In
Normal
★
Taille
USA
Allemagne (EU)*
Prix
Qté
1g
A151117-1g
3 En stock
—
9,90$US
5g
A151117-5g
5 En stock
—
10,90$US
25g
A151117-25g
8 En stock
—

12,90$US

19,90$US
Enregistrer 7,00 $US (35.18%)
100g
A151117-100g
9 En stock
2 En stock

46,90$US

70,90$US
Enregistrer 24,00 $US (33.85%)
500g
A151117-500g
1 En stock
1 En stock

175,90$US

263,90$US
Enregistrer 88,00 $US (33.35%)
Enter a quantity for the sizes you want to add.

Vue d’ensemble

Aceclofenac is a non-steroidal anti-inflammatory drug (NSAID) analog of Diclofenac.
An anti-inflammatory and analgesic agent

Spécifications

Synonymes
2-((2,6-Dichlorophenyl)amino)benzeneacetic acid carboxymethyl ester | ClanzaCR | Cincofen | Hifenac | ACECLOFENAC [MI] | Acide picrique | Aceclofenac | Aceclofenac (TN) | Aceclofenac for peak identification | 2-[(2',6'-dichlorophenyl)amino]phenylacetoxyacetic acid | 2-[(2,6-dichlorophenyl)amino]phenylacetoxyacetic acid | [({2-[(2,6-dichlo Afficher plus
Spécifications et pureté
≥98%(HPLC)
Mécanismes biochimiques et physiologiques
Aceclofenac is an anti-inflammatory analgesic. Aceclofenac is an inhibitor of Cox-1 and Cox-2.Non-steroidal anti-inflammatory. Cyclooxygenase inhibitor. Orally active. Active in vitro and in vivo .
Conditions de stockage de stockage
Room temperature
Expédié en
Normal
Type d'action
INHIBITOR
Mécanisme d'action
Cyclooxygenase-2 inhibitor
Note
Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Toxic, refer to SDS for further information. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Pureté
≥98%(HPLC)
Propriétés du produit
ALogP
4.3
Noms et identifiants
Pubchem Sid
Pubchem Sid Url
https://pubchem.ncbi.nlm.nih.gov/substance/488184674
Sourires canoniques
C1=CC=C(C(=C1)CC(=O)OCC(=O)O)NC2=C(C=CC=C2Cl)Cl
IUPAC Name
2-[2-[2-(2,6-dichloroanilino)phenyl]acetyl]oxyacetic acid
InChIKey
MNIPYSSQXLZQLJ-UHFFFAOYSA-N
INCHI
1S/C16H13Cl2NO4/c17-11-5-3-6-12(18)16(11)19-13-7-2-1-4-10(13)8-15(22)23-9-14(20)21/h1-7,19H,8-9H2,(H,20,21)
Isomères SMILES
C1=CC=C(C(=C1)CC(=O)OCC(=O)O)NC2=C(C=CC=C2Cl)Cl
WGK Allemagne
3
RTECS
CY1577900
Poids moléculaire
354.18
Reaxy-Rn
4884476
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=4884476&ln=

Données avancées

Taxonomic Classification

Taxonomy Tree

KingdomOrganic compounds
SuperclassBenzenoids
ClasseBenzene and substituted derivatives
SubclassHalobenzenes
Intermediate Tree Nodes Chlorobenzenes
Direct ParentDichlorobenzenes
Alternative Parents Aniline and substituted anilines  Dicarboxylic acids and derivatives  Aryl chlorides  Carboxylic acid esters  Amino acids  Secondary amines  Carboxylic acids  Organopnictogen compounds  Organochlorides  Organic oxides  Hydrocarbon derivatives  Carbonyl compounds  
Molecular FrameworkAromatic homomonocyclic compounds
Substituents Aniline or substituted anilines - 1,3-dichlorobenzene - Aryl chloride - Aryl halide - Dicarboxylic acid or derivatives - Amino acid or derivatives - Amino acid - Carboxylic acid ester - Carboxylic acid derivative - Secondary amine - Carboxylic acid - Amine - Organohalogen compound - Organochloride - Organonitrogen compound - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Carbonyl group - Organopnictogen compound - Organic oxygen compound - Organic nitrogen compound - Aromatic homomonocyclic compound
DescriptionThis compound belongs to the class of organic compounds known as dichlorobenzenes. These are compounds containing a benzene with exactly two chlorine atoms attached to it.
External Descriptors monocarboxylic acid - carboxylic ester - secondary amino compound - dichlorobenzene - amino acid
Structure 3D
Modèle de structure chimique interactif





Cibles associées (humaines)
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
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
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)
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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
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
SLC6A3 Tclin Dopamine transporter (10535 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
GRIN1 Tclin Glutamate (NMDA) receptor subunit zeta 1 (122 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
KCNH2 Tclin HERG (29587 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
HTR4 Tclin Serotonin 4 (5-HT4) receptor (2068 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
CACNA1C Tclin Voltage-gated L-type calcium channel alpha-1C subunit (766 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Cibles associées (non humaines)
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
Ttr Transthyretin (14 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
Pde4d Phosphodiesterase 4D (4 Activities)
Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID
Nos2 Nitric oxide synthase, inducible (3573 Activities)
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Mapk1 MAP kinase ERK2 (650 Activities)
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Hdac6 Histone deacetylase 6 (222 Activities)
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Mmp9 Matrix metalloproteinase 9 (38 Activities)
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Pneumocystis carinii (749 Activities)
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Leishmania infantum (5912 Activities)
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Trypanosoma brucei (78846 Activities)
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Trypanosoma brucei brucei (13300 Activities)
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Entamoeba histolytica (2676 Activities)
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Cryptosporidium parvum (1150 Activities)
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Plasmodium falciparum (966862 Activities)
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Leishmania amazonensis (3813 Activities)
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Leishmania donovani (89745 Activities)
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Leishmania major (2877 Activities)
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Leishmania mexicana (936 Activities)
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Trypanosoma cruzi (99888 Activities)
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Trichomonas vaginalis (2376 Activities)
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Toxoplasma gondii (4585 Activities)
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Rattus norvegicus (775804 Activities)
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rep Replicase polyprotein 1ab (378 Activities)
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Mécanismes d'action
Certificats (CoA, COO, BSE/TSE et tableau d'analyse)
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 TypeDateArticle
K1814025K1814025Certificate of AnalysisJun 11, 2026 A151117
K1814024K1814024Certificate of AnalysisJun 11, 2026 A151117
G2228477G2228477Certificate of AnalysisMay 19, 2026 A151117
G2228478G2228478Certificate of AnalysisMay 19, 2026 A151117
G2228479G2228479Certificate of AnalysisMay 19, 2026 A151117
G2228480G2228480Certificate of AnalysisMay 19, 2026 A151117
E1711014E1711014Certificate of AnalysisJan 16, 2025 A151117
B2624341B2624341Certificate of AnalysisJun 12, 2022 A151117
C2306859C2306859Certificate of AnalysisJun 12, 2022 A151117
E2316908E2316908Certificate of AnalysisJun 12, 2022 A151117
E2316909E2316909Certificate of AnalysisJun 12, 2022 A151117
E2316923E2316923Certificate of AnalysisJun 12, 2022 A151117
Propriétés chimiques et physiques
Indice de réfraction1.64
Point d'ébullition (°C)~486.0° C at 760 mmHg
Point de fusion (°C)149-153°C
Poids moléculaire354.200 g/mol
XLogP34.300
Hydrogen Bond Donor Count2
Hydrogen Bond Acceptor Count5
Rotatable Bond Count7
Exact Mass353.022 Da
Monoisotopic Mass353.022 Da
Topological Polar Surface Area75.600 Ų
Heavy Atom Count23
Formal Charge0
Complexity411.000
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
FAQ et articles
Citations of This Product
Calculateurs de solution
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