크기 선택
5 G
₩573,272
25 G
₩2,157,281
₩573,272
구입 가능 여부는 고객센터에 문의하십시오.
모든 사진(3)
크기 선택
보기 변경
5 G
₩573,272
25 G
₩2,157,281
About This Item
실험식(Hill 표기법):
C12H16N2O6
CAS Number:
Molecular Weight:
284.27
EC Number:
MDL number:
UNSPSC 코드:
41106305
PubChem Substance ID:
NACRES:
NA.51
₩573,272
구입 가능 여부는 고객센터에 문의하십시오.
추천 제품
생물학적 소스
synthetic (organic)
분석
≥99% (HPLC)
양식
powder
solubility
water: 50 mg/mL, clear to very slightly hazy, colorless to light yellow
저장 온도
−20°C
SMILES string
CC1(C)O[C@@H]2[C@@H](CO)O[C@H]([C@@H]2O1)N3C=CC(=O)NC3=O
InChI
1S/C12H16N2O6/c1-12(2)19-8-6(5-15)18-10(9(8)20-12)14-4-3-7(16)13-11(14)17/h3-4,6,8-10,15H,5H2,1-2H3,(H,13,16,17)/t6-,8-,9-,10-/m1/s1
InChI key
GFDUSNQQMOENLR-PEBGCTIMSA-N
유사한 제품을 찾으십니까? 방문 제품 비교 안내
애플리케이션
2′,3′-O-Isopropylideneuridine is used in the chemical synthesis of N-benzoylated uridine derivatives and N3-substituted 2′,3′-O-isopropylideneuridines with central nervous system (CNS) depressant activity.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
C S Yao et al.
Chemical & pharmaceutical bulletin, 47(12), 1802-1804 (2000-04-05)
N3-Substituted derivatives of 2',3'-O-isopropylideneuridine (1) were synthesized and their pharmacological effects on the central nervous system (CNS) examined using mice. Methyl (2), ethyl (3), propyl (4), butyl (5), allyl (6), benzyl (7), o-, m-, p-xylyls (8, 9, 10), and alpha-phenylethyl
Tomomi Shimizu et al.
Chemical & pharmaceutical bulletin, 53(3), 313-318 (2005-03-04)
Seventy eight N(3)-substituted derivatives of uridine (1), thymidine (2), 2'-deoxyuridine (3), 6-azauridine (4), 2',3'-O-isopropylideneuridine (5), and arabinofuranosyluracil (6) were synthesized and their antinociceptive effects were evaluated. N(3)-(2',4'-Dimethoxyphenacyl)uridine (1l), N(3)-(2',4'-dimethoxyphenacyl)2'-deoxyuridine (3l), and N(3)-(2',5'-dimethoxyphenacyl)arabinofuranosyluracil (6m) possessed 93, 86, and 82% of the
M L Scholes et al.
International journal of radiation biology, 61(4), 443-449 (1992-04-01)
The effect of pH on base release in the gamma-radiolysis of N2O-saturated solutions of a number of nucleosides (including uridine, 3-methyluridine, 2',3'-O-isopropylidene-uridine, and adenosine) has been investigated. For all these nucleotides, independent of the base or sugar moiety, base release
S I Malekin et al.
Bioorganicheskaia khimiia, 23(8), 648-654 (1997-08-01)
New nucleoside-phospholipid conjugates were synthesized based on 1,2-disubstituted glycerides and nucleosides. These contain rac-1-hexadecyl-2-palmitoyl(or 2-methylcarbamoyl)-sn-glycero-3-phosphate as the phospholipid component and 2',3'-didehydro-3'-deoxythymidine, 1-(Z-5-hydroxypentene-2-yl)thymine, or 2',3'-isopropylideneuridine as a nucleoside component. The conjugates were synthesized by three different ways: from rac-1-hexadecyl-2-acyl-sn-glycero-3-phospodichlorides, -3-phosphatidic acids
Anita R Maguire et al.
Carbohydrate research, 337(4), 369-372 (2002-02-14)
An improved procedure for the synthesis of N-benzoyl-2',3'-O-isopropylidene uridine via one-step selective N-benzoylation of 2',3' -O-isopropylidene uridine has been developed. An efficient synthetic route to N-benzoyl thymidine via initial tribenzoylation, followed by selective hydrolysis of the benzoates is also described.
활성 필터
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.
