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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
Molecular Weight:
321.35
MDL Number:
MOL File:
321695-57-2.mol
MSDS File:
SDS
Last updated:2023-09-04 16:42:00

NSC764414 Properties

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

SAFETY

Risk and Safety Statements

WGK Germany  3

NSC764414 price More Price(22)

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

NSC764414 Chemical Properties,Uses,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

NSC764414 Suppliers

Global( 44)Suppliers
Supplier Tel Email Country ProdList Advantage
TargetMol Chemicals Inc.
+1-781-999-5354 +1-00000000000 marketing@targetmol.com United States 19892 58
Career Henan Chemica Co
+86-0371-86658258 +8613203830695 laboratory@coreychem.com China 30250 58
Aladdin Scientific
+1-+1(833)-552-7181 sales@aladdinsci.com United States 57511 58
Amadis Chemical Company Limited
571-89925085 sales@amadischem.com China 131980 58
Sigma-Aldrich 021-61415566 800-8193336 orderCN@merckgroup.com China 51471 80
Pharmacodia (Beijing) Co.,Ltd +86-400-851-9921 sales@pharmacodia.com China 2317 55
Shanghai EFE Biological Technology Co., Ltd. 021-65675885 18964387627 info@efebio.com China 9707 58
Tianjin Kailiqi Biotechnology Co., Ltd. 15076683720 klq@cw-bio.com China 4182 55
ShangHai Biochempartner Co.,Ltd 17754423994 17754423994 2853530910@QQ.com China 8014 62
Lynnchem 86-(0)29-85992781 17792393971 info@lynnchem.com China 4587 58

NSC764414 Spectrum

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