ChemicalBook > CAS DataBase List > NSC764414

NSC764414

Product Name
NSC764414
CAS No.
321695-57-2
Chemical Name
NSC764414
Synonyms
L002;NSC764414;L002(NSC764414);p300/CBP Inhibitor VI, L002;L 002;NSC 764414;L-002;NSC-764414;p300/CBP Inhibitor VI, L002 - CAS 321695-57-2 - Calbiochem;4-[O-[(4-Methoxyphenyl)sulfonyl]oxime]-2,6-dimethyl-2,5-cyclohexadiene-1,4-dione;[(3,5-dimethyl-4-oxo-cyclohexa-2,5-dien-1-ylidene)amino] 4-methoxybenzenesulfonate;2,5-Cyclohexadiene-1,4-dione, 2,6-dimethyl-, 4-[O-[(4-methoxyphenyl)sulfonyl]oxime];p300,acetylation,L 002,Inhibitor,HATs,L-002,HAT,inhibit,fibrosis,L002,Histone Acetyltransferase,STAT,cardiac,histone
CBNumber
CB42750596
Molecular Formula
C15H15NO5S
Formula Weight
321.35
MOL File
321695-57-2.mol
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NSC764414 Property

Boiling point:
459.8±55.0 °C(Predicted)
Density 
1.28±0.1 g/cm3(Predicted)
storage temp. 
2-8°C
solubility 
DMSO: soluble20mg/mL, clear
form 
powder
color 
white to beige
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Safety

WGK Germany 
3
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Hazard and Precautionary Statements (GHS)

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N-Bromosuccinimide Price

Sigma-Aldrich
Product number
SML0759
Product name
L002
Purity
≥98% (HPLC)
Packaging
5mg
Price
$105
Updated
2024/03/01
Sigma-Aldrich
Product number
5.05298
Product name
p300/CBP Inhibitor VI, L002 - CAS 321695-57-2 - Calbiochem
Packaging
10MG
Price
$138
Updated
2023/01/07
Sigma-Aldrich
Product number
SML0759
Product name
L002
Purity
≥98% (HPLC)
Packaging
25mg
Price
$377
Updated
2022/05/15
Cayman Chemical
Product number
17778
Product name
L002
Purity
≥98%
Packaging
5mg
Price
$81
Updated
2024/03/01
Cayman Chemical
Product number
17778
Product name
L002
Purity
≥98%
Packaging
10mg
Price
$120
Updated
2024/03/01
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NSC764414 Chemical Properties,Usage,Production

Description

L002 is an inhibitor of p300 histone acetyltransferase (KAT3B; IC50 = 1.98 μM in vitro). It has weaker inhibitory effects against PCAF and GCN5 (IC50s = 35 and 34 μM, respectively) and is specific for p300 over a panel of additional acetyltransferases, deacetylases, and methyltransferases. L002 blocks acetylation of histones and p53 in cells treated with trichostatin A or etoposide, respectively, and reduces STAT3 phosphorylation, which requires p300-mediated acetylation of STAT3. It induces growth arrest and apoptosis in certain cancer cell lines and, when administered intraperitoneally in mice, suppresses the growth of triple-negative breast cancer xenografts.

Uses

L002 is an inhibitor of p300 histone acetyl transferase, which maintains weaker inhibitory effects against PCAF and GCN5. and is specific for p3000.

Biochem/physiol Actions

L002 (NSC764414) is an inhibitor of acetyltransferase p300, a lysine acetyltransferase that catalyzes acetyl group attachment to lysine residues of a variety of proteins including histones and p53, and acts as a critical coactivator of several oncogenic transcription factors involved in cancer cell survival and proliferation including STAT3, NF-kB, and hypoxia-inducible factor-1α (HIF-1α). L002 (NSC764414) was discovered from compounds assayed for cytotoxicity to the triple-negative breast cancer (TNBC) cell line MDA-MB-231 but not to the human mammary epithelial cells, then further screened for inhibition of p300. L002 has an in vitro IC50 of 1.98 μM for p300 with lesser inhibition of the GNAT (GCN5-related N-acetyltransferase) family, and no inhibition against the MYST family of histone acetyltransferases (HATs), histone deacetylases (HDACs), or histone methyltransferases (HMTs). L002 potently suppressed tumor growth and histone acetylation of MDA-MB-468 xenografts and leukemia and lymphoma cell lines.

NSC764414 Preparation Products And Raw materials

Raw materials

Preparation Products

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NSC764414 Suppliers

Sigma-Aldrich
Tel
021-61415566 800-8193336
Email
orderCN@merckgroup.com
Country
China
ProdList
51471
Advantage
80
Pharmacodia (Beijing) Co.,Ltd
Tel
+86-400-851-9921
Fax
+86-10-82826195
Email
sales@pharmacodia.com
Country
China
ProdList
2317
Advantage
55
Shanghai EFE Biological Technology Co., Ltd.
Tel
021-65675885 18964387627
Fax
021-65675885
Email
info@efebio.com
Country
China
ProdList
9709
Advantage
58
Tianjin Kailiqi Biotechnology Co., Ltd.
Tel
15076683720
Fax
022-23754520
Email
klq@cw-bio.com
Country
China
ProdList
3445
Advantage
55
ShangHai Biochempartner Co.,Ltd
Tel
17754423994 17754423994
Fax
QQ:2853530913
Email
2853530910@QQ.com
Country
China
ProdList
8013
Advantage
62
Amadis Chemical Company Limited
Tel
571-89925085
Fax
0086-571-89925065
Email
sales@amadischem.com
Country
China
ProdList
131981
Advantage
58
Lynnchem
Tel
86-(0)29-85992781 17792393971
Email
info@lynnchem.com
Country
China
ProdList
4587
Advantage
58
Novachemistry
Tel
44-20819178-90 02081917890
Fax
(0)2080432064
Email
info@novachemistry.com
Country
United Kingdom
ProdList
4381
Advantage
58
Fan De(Beijing) Biotechnology Co., Ltd.
Tel
15911056312
Email
liming@bio-fount.com
Country
China
ProdList
9730
Advantage
58
TargetMol Chemicals Inc.
Tel
+1-781-999-5354 +1-00000000000
Email
marketing@targetmol.com
Country
United States
ProdList
19892
Advantage
58

321695-57-2, NSC764414Related Search:


  • 4-[O-[(4-Methoxyphenyl)sulfonyl]oxime]-2,6-dimethyl-2,5-cyclohexadiene-1,4-dione
  • L002
  • NSC764414
  • p300/CBP Inhibitor VI, L002
  • [(3,5-dimethyl-4-oxo-cyclohexa-2,5-dien-1-ylidene)amino] 4-methoxybenzenesulfonate
  • L002(NSC764414)
  • L 002;NSC 764414;L-002;NSC-764414
  • p300/CBP Inhibitor VI, L002 - CAS 321695-57-2 - Calbiochem
  • p300,acetylation,L 002,Inhibitor,HATs,L-002,HAT,inhibit,fibrosis,L002,Histone Acetyltransferase,STAT,cardiac,histone
  • 2,5-Cyclohexadiene-1,4-dione, 2,6-dimethyl-, 4-[O-[(4-methoxyphenyl)sulfonyl]oxime]
  • 321695-57-2