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890-38-0

中文名稱 2'-脫氧肌苷
英文名稱 2'-Deoxyinosine
CAS 890-38-0
EINECS 編號(hào) 212-964-1
分子式 C10H12N4O4
MDL 編號(hào) MFCD00005762
分子量 252.23
MOL 文件 890-38-0.mol
更新日期 2024/10/25 14:54:02
890-38-0 結(jié)構(gòu)式 890-38-0 結(jié)構(gòu)式

基本信息

中文別名
2ˊ-脫氧次黃嘌呤核苷
2ˊ-脫氧肌苷
9-(2-脫氧-Β-D-呋喃核糖基)次黃嘌呤
英文別名
2'-DEOXYINOSINE
9-(2-DEOXY-BETA-D-RIBOFURANOSYL)HYPOXANTHINE
DEOXYINOSINE, 2'-
DI
2’-deoxy-inosin
Deoxyinosine
Hypoxanthine, 9-(2-deoxy-beta-D-erythro-pentofuranosyl)-
9-(2-deoxy-β-d-ribofuranosyl)hypoxanthine
2'-Deoxy-D-inosine
9-[4-hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one
DEOXYINOSINE, 2'-(P)
2''-DEOXYINOSINE Crystalline
9-(4-Hydroxy-5-hydroxymethyl-tetrahydro-furan-2-yl)-1,9-dihydropurin-6-one
2-DEOXYINOSINE extrapure
9-[(2R,4S,5R)-4-Hydroxy-5-(hydroxymethyl)oxolan-2-yl]-3H-purin-6-one
Inosine, 2'-deoxy-
所屬類別
生物化工:核苷酸及其類似物

物理化學(xué)性質(zhì)

外觀性狀白色粉末,可溶于甲醇、乙醇、DMSO等有機(jī)溶劑。
熔點(diǎn)250 °C
比旋光度21 º (c=1, H2O 22 ºC)
沸點(diǎn)395.4°C (rough estimate)
密度1.3402 (rough estimate)
折射率-16 ° (C=1, H2O)
儲(chǔ)存條件−20°C
溶解度DMSO (Slightly), Waterh (Slightly)
酸度系數(shù)(pKa)8.92±0.70(Predicted)
形態(tài)粉末
顏色白色至灰白色
水溶解性8.33g/L(25.02 ºC)
BRN33517
InChIInChI=1S/C10H12N4O4/c15-2-6-5(16)1-7(18-6)14-4-13-8-9(14)11-3-12-10(8)17/h3-7,15-16H,1-2H2,(H,11,12,17)/t5-,6+,7+/m0/s1
InChIKeyVGONTNSXDCQUGY-RRKCRQDMSA-N
SMILESOC[C@H]1O[C@@H](N2C3C(=C(N=CN=3)O)N=C2)C[C@@H]1O
CAS 數(shù)據(jù)庫890-38-0(CAS DataBase Reference)
NIST化學(xué)物質(zhì)信息Inosine, 2'-deoxy-(890-38-0)

安全數(shù)據(jù)

危險(xiǎn)性符號(hào)(GHS)GHS hazard pictograms
GHS07
警示詞警告
危險(xiǎn)性描述H302-H315-H319
危險(xiǎn)品標(biāo)志Xn,Xi
危險(xiǎn)類別碼20/21/22-36/37/38
安全說明S24/25
WGK Germany3
海關(guān)編碼29349990

化學(xué)品安全說明書(MSDS)

知名試劑公司產(chǎn)品信息

Acros Organics
TCI Shanghai
2'-脫氧肌苷價(jià)格(試劑級)
報(bào)價(jià)日期產(chǎn)品編號(hào)產(chǎn)品名稱CAS號(hào)包裝價(jià)格
2024/08/19H522922'-脫氧肌苷, 98+%
2'-Deoxyinosine, 98+%
890-38-0250mg178元
2024/08/19H522922'-脫氧肌苷, 98+%
2'-Deoxyinosine, 98+%
890-38-01g731元
2024/08/19H522922'-脫氧肌苷, 98+%
2'-Deoxyinosine, 98+%
890-38-05g3659元

常見問題列表

生物活性
2’-deoxyadenosine 能夠抑制人癌細(xì)胞株的生長,并發(fā)現(xiàn)其與嘌呤核苷磷酸化酶 (PNP) 缺乏有關(guān)。
靶點(diǎn)

Human Endogenous Metabolite

體外研究

In the absence of deoxycoformycin, 2’-deoxyadenosine is primarily deaminated to 2’-deoxyinosine and then converted into hypoxanthine. In the presence of the inhibitor, the deoxynucleoside, in addition to a phosphorylation process, undergoes phosphorolytic cleavage giving rise to adenine. The conversion of 2’-deoxyadenosine to adenine might represent a protective device, emerging when the activity of adenosine deaminase is reduced or inhibited. There is much evidence to indicate that the enzyme catalyzing this processs may be distinct from methylthioadenosine phosphorylase and S-adenosyl homocysteine hydrolase, which are the enzymes reported to be responsible for the formation of adenine from 28-deoxyadenosine in mammals.

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