NEO2734 - 10mM in DMSO , CAS No.2081072-29-7

CAS: 2081072-29-7 Cat. No.: N492067 분자식: C22H24F3N3O3 분자량: 435.44
주문 가능
GRADE & PURITY 10mM in DMSO
Synonyms
EP316702 | 1,​3-​dimethyl-​5-​[2-​(tetrahydro-​2H-​pyran-​4-​yl)​-​1-​[2-​(trifluoromethoxy)​ethyl]​-​1H-​benzimidazol-​6-​yl]​- (1H)​-​Pyridinone
Storage
Store at -80°C
Shipped In
Dry ice packs + Cold packs
★
Size
USA
독일 (EU)*
Price
Qty
1ml
N492067-1ml
2 재고 있음
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US$941.90

US$1,374.90
저장 US$433.00 (31.49%)
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Why this grade

10mM in DMSO for sensitive chromatographic and analytical workflows requiring minimal baseline interference.

🌡

Storage & shipping

Store at -80°C Ships Dry ice packs + Cold packs Check lot-specific COA for exact specifications.

📋

Quality documents

SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.

📚

Literature proof

Cited in 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.

개요

Information

NEO2734 NEO2734 (EP31670) is a novel, orally active and selective dual inhibitor of p300/CBP and BET bromodomain with IC50 of both <30 nM.


Targets

p300/CBP (Cell-free assay); BET (Cell-free assay) <30 nM; <30 nM


In vitro

Treatment of NMC cells with the novel dual p300/CBP and BET bromodomain–selective inhibitor, NEO2734, potently inhibits growth and induces differentiation of NMC cells in vitro; findings that correspond with potentiated transcriptional effects from combined BET and p300 bromodomain inhibition.


In vivo

In three disseminated NMC xenograft models, NEO2734 provides greater growth inhibition, with tumor regression and significant survival benefit seen in two of three models, compared with a lead clinical BET inhibitor or “standard” chemotherapy.


Cell Research(from reference)

Cell lines:NUT carcinoma patient cell lines (TC-797, 14169, 10-15, PER-403) 

Concentrations:1 μM 

Incubation Time:24 h 

Specifications

동의어
EP316702 | 1,​3-​dimethyl-​5-​[2-​(tetrahydro-​2H-​pyran-​4-​yl)​-​1-​[2-​(trifluoromethoxy)​ethyl]​-​1H-​benzimidazol-​6-​yl]​- (1H)​-​Pyridinone
사양 및 순도
10mM in DMSO
생화학 및 생리적 메커니즘
NEO2734 (EP31670) is a novel, orally active and selective dual inhibitor of p300/CBP and BET bromodomain with IC50 of both <30 nM.
보관 조건
Store at -80°C
배송
Dry ice packs + Cold packs
이 제품은 콜드 체인 배송이 필요합니다.지상 및 기타 경제 서비스는 사용할 수 없습니다.
작업 유형
INHIBITOR
이름과 식별자
Pubchem Sid
정식 스마일
CC1=CC(=CN(C1=O)C)C2=CC3=C(C=C2)N=C(N3CCOC(F)(F)F)C4CCOCC4
IUPAC Name
1,3-dimethyl-5-[2-(oxan-4-yl)-3-[2-(trifluoromethoxy)ethyl]benzimidazol-5-yl]pyridin-2-one
InChIKey
KPWWFNXRLAAREN-UHFFFAOYSA-N
INCHI
1S/C22H24F3N3O3/c1-14-11-17(13-27(2)21(14)29)16-3-4-18-19(12-16)28(7-10-31-22(23,24)25)20(26-18)15-5-8-30-9-6-15/h3-4,11-13,15H,5-10H2,1-2H3
분자량
435.44
Reaxy-Rn
30909951
Reaxys-RN_link_address
https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=30909951&ln=

Documentation

📋 Safety Data Sheet (SDS)

Comprehensive hazard, handling, storage, and regulatory compliance document.

Download SDS →

✅ Certificate of Analysis (COA)

Lot-specific quality data. Enter your lot number to retrieve the exact COA.

Look up COA →

📊 Datasheet

Quick-reference summary of product specifications and applications.

View datasheet →

🔬 Specification Sheet

Full quality attributes and acceptance criteria for this grade.

View spec sheet →

Advanced Data

3D 구조
상호 작용 화학 구조 모델





인증서(CoA, COO, BSE/TSE 및 분석 차트)
C of A & Other Certificates(BSE/TSE, COO):
Analytical Chart:
화학 및 물리적 특성
용해성Solubility (25°C) In vitro DMSO: 87 mg/mL (199.79 mM); Ethanol: 87 mg/mL (199.79 mM); Water: Insoluble;
분자량435.400 g/mol
XLogP32.900
Hydrogen Bond Donor Count0
Hydrogen Bond Acceptor Count7
Rotatable Bond Count5
Exact Mass435.177 Da
Monoisotopic Mass435.177 Da
Topological Polar Surface Area56.600 Ų
Heavy Atom Count31
Formal Charge0
Complexity733.000
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
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