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Santacruzamate A - ≥98%(HPLC), high purity , CAS No.1477949-42-0, Inhibitor of histone deacetylase 2;Inhibitor of histone deacetylase 4;Inhibitor of histone deacetylase 6

  • Moligand™
  • ≥98%(HPLC)
Item Number
S288868
Grouped product items
SKUSizeAvailabilityPrice Qty
S288868-10mg
10mg
In stock
$63.90
S288868-50mg
50mg
In stock
$246.90
S288868-100mg
100mg
In stock
$370.90

Highly potent and selective HDAC2 inhibitor

Basic Description

Synonymssantacruzamate A|1477949-42-0|CAY10683|Santacruzamate A (CAY10683)|CAY10683 (SantacruzaMate A)|ethyl N-[4-oxo-4-(2-phenylethylamino)butyl]carbamate|Ethyl (4-oxo-4-(phenethylamino)butyl)carbamate|CAY10683(Santacruzamate A)|CHEMBL3086767|Carbamic acid, N-[4
Specifications & PurityMoligand™, ≥98%(HPLC)
Biochemical and Physiological MechanismsHighly potent and selective histone deactylase 2 (HDAC2) inhibitor (IC50= 112 - 119 pM). Also inhibits HDAC6 in nanomolar range (IC50= 433 nM). Displays >3500 fold selectivity for HDAC2 over HDAC6, and >8500-fold selectivity over HDAC4 (IC50>1 μM for HDAC
Storage TempStore at -20°C
Shipped InIce chest + Ice pads
GradeMoligand™
Action TypeINHIBITOR
Mechanism of actionInhibitor of histone deacetylase 2;Inhibitor of histone deacetylase 4;Inhibitor of histone deacetylase 6

Associated Targets

DNMT3A Tclin DNA (cytosine-5)-methyltransferase 3A 0 Activities

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

DNMT3B Tchem DNA (cytosine-5)-methyltransferase 3B 0 Activities

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

DNMT1 Tclin DNA (cytosine-5)-methyltransferase 1 0 Activities

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

HDAC4 Tclin Histone deacetylase 4 1 Activities

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

HDAC6 Tclin Histone deacetylase 6 3 Activities

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

HDAC1 Tclin Histone deacetylase 1 0 Activities

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

HDAC7 Tclin Histone deacetylase 7 0 Activities

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

HDAC11 Tclin Histone deacetylase 11 0 Activities

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

HDAC9 Tclin Histone deacetylase 9 0 Activities

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

HDAC2 Tclin Histone deacetylase 2 3 Activities

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

SIRT5 Tchem NAD-dependent protein deacylase sirtuin-5, mitochondrial 0 Activities

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

SIRT3 Tchem NAD-dependent protein deacetylase sirtuin-3, mitochondrial 0 Activities

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

SIRT2 Tchem NAD-dependent protein deacetylase sirtuin-2 0 Activities

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

SIRT1 Tchem NAD-dependent protein deacetylase sirtuin-1 0 Activities

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

HDAC10 Tclin Histone deacetylase 10 0 Activities

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

HDAC8 Tclin Histone deacetylase 8 0 Activities

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

HDAC5 Tclin Histone deacetylase 5 0 Activities

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

HDAC3 Tclin Histone deacetylase 3 0 Activities

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

Names and Identifiers

IUPAC Name ethyl N-[4-oxo-4-(2-phenylethylamino)butyl]carbamate
INCHI InChI=1S/C15H22N2O3/c1-2-20-15(19)17-11-6-9-14(18)16-12-10-13-7-4-3-5-8-13/h3-5,7-8H,2,6,9-12H2,1H3,(H,16,18)(H,17,19)
InChi Key HTOYBIILVCHURC-UHFFFAOYSA-N
Canonical SMILES CCOC(=O)NCCCC(=O)NCCC1=CC=CC=C1
Isomeric SMILES CCOC(=O)NCCCC(=O)NCCC1=CC=CC=C1
PubChem CID 72946782
Molecular Weight 278.35

Certificates

Certificate of Analysis(COA)

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3 results found

Lot NumberCertificate TypeDateItem
I2216327Certificate of AnalysisJul 04, 2022 S288868
I2216415Certificate of AnalysisJul 04, 2022 S288868
I2216648Certificate of AnalysisJul 04, 2022 S288868

Chemical and Physical Properties

SolubilitySolvent:DMSO, Max Conc. mg/mL: 27.84, Max Conc. mM: 100

Related Documents

References

1. Pavlik CM, Wong CY, Ononye S, Lopez DD, Engene N, McPhail KL, Gerwick WH, Balunas MJ.  (2013)  Santacruzamate A, a potent and selective histone deacetylase inhibitor from the Panamanian marine cyanobacterium cf. Symploca sp..  J Nat Prod,  76  (11): (2026-33).  [PMID:24164245]

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