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Chlorogenic acid - 95%, high purity , CAS No.327-97-9, Inhibitor of protein tyrosine phosphatase non-receptor type 1

  • Moligand™
  • ≥95%
Item Number
C109402
Grouped product items
SKUSizeAvailabilityPrice Qty
C109402-250mg
250mg
In stock
$24.90
C109402-1g
1g
In stock
$69.90
C109402-5g
5g
In stock
$239.90
C109402-10g
10g
In stock
$389.90
C109402-25g
25g
Available within 4-8 weeks(?)
Items will be manufactured post-order and can take 4-8 weeks. Thank you for your patience!
$779.90

Basic Description

SynonymsCHLOROGENIC ACID|327-97-9|3-O-Caffeoylquinic acid|Heriguard|Chlorogenate|3-(3,4-Dihydroxycinnamoyl)quinic acid|3-Caffeoylquinic acid|Hlorogenic acid|trans-Chlorogenic acid|CP chlorogenic acid|Caffeoyl quinic acid|Chlorogenicacid|NSC-407296|5-CQA|(+)-Chlor
Specifications & PurityMoligand™, ≥95%
Shipped InNormal
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of protein tyrosine phosphatase non-receptor type 1

Associated Targets

DUSP3 Tchem Dual specificity protein phosphatase 3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

EHMT2 Tchem Histone-lysine N-methyltransferase EHMT2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GMNN Tbio Geminin 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTPN2 Tchem Tyrosine-protein phosphatase non-receptor type 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTPN11 Tchem Tyrosine-protein phosphatase non-receptor type 11 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTPN1 Tchem Tyrosine-protein phosphatase non-receptor type 1 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTPN6 Tchem Tyrosine-protein phosphatase non-receptor type 6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SRC Tclin Proto-oncogene tyrosine-protein kinase Src 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RAPGEF3 Tchem Rap guanine nucleotide exchange factor 3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

RAPGEF4 Tchem Rap guanine nucleotide exchange factor 4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

STAT3 Tchem Signal transducer and activator of transcription 3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

STAT1 Tchem Signal transducer and activator of transcription 1-alpha/beta 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

STAT5B Tchem Signal transducer and activator of transcription 5B 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLC37A4 Tchem Glucose-6-phosphate exchanger SLC37A4 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

HDAC6 Tclin Histone deacetylase 6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLCO1B1 Tchem Solute carrier organic anion transporter family member 1B1 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

SLCO1B3 Tchem Solute carrier organic anion transporter family member 1B3 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A9 Tbio UDP-glucuronosyltransferase 1-9 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

TTR Tclin Transthyretin 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

LPO Tbio Lactoperoxidase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PTGS2 Tclin Prostaglandin G/H synthase 2 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

LCK Tclin Tyrosine-protein kinase Lck 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

ACHE Tclin Acetylcholinesterase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AKR1B10 Tchem Aldo-keto reductase family 1 member B10 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

AKR1B1 Tclin Aldose reductase 1 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

APP Tclin Amyloid-beta A4 protein 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

UGT1A6 Tbio UDP-glucuronosyltransferase 1-6 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

F2 Tclin Prothrombin 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

BCHE Tclin Cholinesterase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

GLS Tchem Glutaminase kidney isoform, mitochondrial 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

PLA2G7 Tchem Platelet-activating factor acetylhydrolase 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

KDM4A Tchem Lysine-specific demethylase 4A 0 Activities

Activity TypeActivity Value -log(M)Mechanism of ActionActivity ReferencePublications (PubMed IDs)

Names and Identifiers

IUPAC Name (1S,3R,4R,5R)-3-[(E)-3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1,4,5-trihydroxycyclohexane-1-carboxylic acid
INCHI InChI=1S/C16H18O9/c17-9-3-1-8(5-10(9)18)2-4-13(20)25-12-7-16(24,15(22)23)6-11(19)14(12)21/h1-5,11-12,14,17-19,21,24H,6-7H2,(H,22,23)/b4-2+/t11-,12-,14-,16+/m1/s1
InChi Key CWVRJTMFETXNAD-JUHZACGLSA-N
Canonical SMILES O[C@@H]1C[C@](O)(C[C@@H](OC(=O)\C=C\c2ccc(O)c(O)c2)[C@@H]1O)C(O)=O
Isomeric SMILES C1[C@H]([C@H]([C@@H](C[C@@]1(C(=O)O)O)OC(=O)/C=C/C2=CC(=C(C=C2)O)O)O)O
WGK Germany 3
PubChem CID 1794427
Molecular Weight 354.31

Certificates

Certificate of Analysis(COA)

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28 results found

Lot NumberCertificate TypeDateItem
H2413422Certificate of AnalysisAug 21, 2024 C109402
H2413421Certificate of AnalysisAug 21, 2024 C109402
H2413420Certificate of AnalysisAug 21, 2024 C109402
H2413419Certificate of AnalysisAug 21, 2024 C109402
E2413220Certificate of AnalysisMay 17, 2024 C109402
E2413223Certificate of AnalysisMay 17, 2024 C109402
G2401045Certificate of AnalysisMay 17, 2024 C109402
E2413224Certificate of AnalysisMay 17, 2024 C109402
E2413199Certificate of AnalysisMay 17, 2024 C109402
J2330332Certificate of AnalysisNov 02, 2023 C109402
J2330331Certificate of AnalysisNov 02, 2023 C109402
J2330330Certificate of AnalysisNov 02, 2023 C109402
J2330311Certificate of AnalysisNov 02, 2023 C109402
H2325320Certificate of AnalysisAug 31, 2023 C109402
H2325322Certificate of AnalysisAug 31, 2023 C109402
H2325321Certificate of AnalysisAug 31, 2023 C109402
H2325319Certificate of AnalysisAug 31, 2023 C109402
H2325318Certificate of AnalysisAug 31, 2023 C109402
H2325317Certificate of AnalysisAug 31, 2023 C109402
H2325289Certificate of AnalysisAug 31, 2023 C109402
H2325288Certificate of AnalysisAug 31, 2023 C109402
H2325287Certificate of AnalysisAug 31, 2023 C109402
G2308176Certificate of AnalysisJul 13, 2023 C109402
L2210436Certificate of AnalysisDec 16, 2022 C109402
L2210438Certificate of AnalysisDec 16, 2022 C109402
G2220471Certificate of AnalysisJan 12, 2022 C109402
G2220470Certificate of AnalysisJan 12, 2022 C109402
J2113510Certificate of AnalysisOct 18, 2021 C109402

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Chemical and Physical Properties

SolubilitySoluble in water; Very soluble in Acetone,Alcohol
Specific Rotation[α]-37 ° (C=1, H2O)
Melt Point(°C)210°C

Safety and Hazards(GHS)

WGK Germany 3
Merck Index 2142

Related Documents

References

1. Selenge E, Murata T, Kobayashi K, Batkhuu J, Yoshizaki F.  (2013)  Flavone tetraglycosides and benzyl alcohol glycosides from the Mongolian medicinal plant Dracocephalum ruyschiana..  J Nat Prod,  76  (2): (186-93).  [PMID:23356964]
2. Murai T, Matsuda S.  (2023)  The Chemopreventive Effects of Chlorogenic Acids, Phenolic Compounds in Coffee, against Inflammation, Cancer, and Neurological Diseases..  Molecules,  28  (5): (589-97).  [PMID:36903626]
3. Hibi M.  (2023)  Potential of Polyphenols for Improving Sleep: A Preliminary Results from Review of Human Clinical Trials and Mechanistic Insights..  Nutrients,  15  (5): (589-97).  [PMID:36904255]

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