成人免费xx,国产又黄又湿又刺激不卡网站,成人性视频app菠萝网站,色天天天天

Home Cart 0 Sign in  

[ CAS No. 2623-87-2 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
HazMat Fee +

There will be a HazMat fee per item when shipping a dangerous goods. The HazMat fee will be charged to your UPS/DHL/FedEx collect account or added to the invoice unless the package is shipped via Ground service. Ship by air in Excepted Quantity (each bottle), which is up to 1g/1mL for class 6.1 packing group I or II, and up to 25g/25ml for all other HazMat items.

Type HazMat fee for 500 gram (Estimated)
Excepted Quantity USD 0.00
Limited Quantity USD 15-60
Inaccessible (Haz class 6.1), Domestic USD 80+
Inaccessible (Haz class 6.1), International USD 150+
Accessible (Haz class 3, 4, 5 or 8), Domestic USD 100+
Accessible (Haz class 3, 4, 5 or 8), International USD 200+
Chemical Structure| 2623-87-2
Chemical Structure| 2623-87-2
Structure of 2623-87-2 * Storage: {[proInfo.prStorage]}

Please Login or Create an Account to: See VIP prices and availability

Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Search after Editing

* Storage: {[proInfo.prStorage]}

* Shipping: {[proInfo.prShipping]}

Quality Control of [ 2623-87-2 ]

Related Doc. of [ 2623-87-2 ]

Alternatived Products of [ 2623-87-2 ]
Product Citations

Product Citations

Zhao, Yue ; Lyu, Zhigang ; Prather, Benjamin , et al. DOI:

Abstract: Dysregulated sialic acid biosynthesis is characteristic of the onset and progression of human diseases including hormone-sensitive prostate cancer and breast cancer. The sialylated glycoconjugates involved in this process are therefore important targets for identification and functional studies. To date, one of the most common strategies is metabolic glycoengineering, which utilizes N-acetylmannosamine (ManNAc) analogues such as N-azidoacetylmannosamine (ManNAz) to hijack sialic acid biosynthesis and label the sialylated glycoconjugates with "click chemistry (CuAAC)" tags. Yet, current chemical modifications including those CuAAC-based alkyne/azide tags are still big in size, and the resulting steric hindrance perturbs the mannosamine and sialic acid derivatives' recognition and metabolism by enzymes involved in biosynthetic pathways. As a result, the peracetylated ManNAz has compromised incorporation to sialic acid substrates and manifests cellular growth inhibition and cytotoxicity. Herein, we show that the α-fluorinated peracetylated analogue ManN(F-Ac) displayed a satisfying safety profile in mammalian cell lines at concentrations as high as 500 μM. More importantly, aliphatic selenol-containing probes can efficiently displace α-fluorine in fluoroacetamide-containing substrates including ManN(F-Ac) at a neutral pH range (~7.2). The combined use of peracetylated ManN(F-Ac) and the dethiobiotin-selenol probe as the fluorine-selenol displacement reaction (FSeDR) toolkit allowed for successful metabolic labeling of sialoglycoproteins in multiple prostate and cancer cell lines, including PC-3 and MDA-MB-231. More sialoglycoproteins in these cell lines were demonstrated to be labeled by FSeDR compared with the traditional CuAAC approach. Lastly, with FSeDR-mediated metabolic labeling, we were able to probe the cellular expression level and spatial distribution of sialylated glycoconjugates during the progression of these hormone-sensitive cancer cells. Taken together, the promising results suggest the potential of the FSeDR strategy to efficiently and systematically identify and study sialic acid substrates and potentially empower metabolic engineering on a diverse set of glycosylated proteins that are vital for human diseases.

Keywords: metabolic engineering ; mannosamine ; sialic acid ; glycobiology ; fluorine displacement reaction ; selenium ; fluorine-selenol displacement reaction (FSeDR)

Purchased from AmBeed: ; ; ;

Product Details of [ 2623-87-2 ]

CAS No. :2623-87-2 MDL No. :MFCD00002817
Formula : C4H7BrO2 Boiling Point : No data available
Linear Structure Formula :CH2BrCH2CH2COOH InChI Key :GRHQDJDRGZFIPO-UHFFFAOYSA-N
M.W : 167.00 Pubchem ID :75809
Synonyms :

Calculated chemistry of [ 2623-87-2 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 7
Num. arom. heavy atoms : 0
Fraction Csp3 : 0.75
Num. rotatable bonds : 3
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 30.98
TPSA : 37.3 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : No
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.74 cm/s

Lipophilicity

Log Po/w (iLOGP) : 1.27
Log Po/w (XLOGP3) : 0.81
Log Po/w (WLOGP) : 1.25
Log Po/w (MLOGP) : 1.09
Log Po/w (SILICOS-IT) : 0.83
Consensus Log Po/w : 1.05

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 2.0
Bioavailability Score : 0.56

Water Solubility

Log S (ESOL) : -1.19
Solubility : 10.8 mg/ml ; 0.0649 mol/l
Class : Very soluble
Log S (Ali) : -1.18
Solubility : 11.2 mg/ml ; 0.0668 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -1.31
Solubility : 8.12 mg/ml ; 0.0486 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.72

Safety of [ 2623-87-2 ]

Signal Word:Danger Class:8
Precautionary Statements:P280-P305+P351+P338-P310 UN#:3261
Hazard Statements:H314 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 2623-87-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 2623-87-2 ]

[ 2623-87-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2623-87-2 ]
  • [ 2848-01-3 ]
  • C19H22O4P(1+)*Br(1-) [ No CAS ]
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Related Functional Groups of
[ 2623-87-2 ]

Aliphatic Chain Hydrocarbons

Chemical Structure| 30515-28-7

[ 30515-28-7 ]

7-Bromoheptanoic acid

Similarity: 0.95

Chemical Structure| 2067-33-6

[ 2067-33-6 ]

5-Bromopentanoic acid

Similarity: 0.95

Chemical Structure| 2536-35-8

[ 2536-35-8 ]

16-Bromohexadecanoic acid

Similarity: 0.95

Chemical Structure| 41059-02-3

[ 41059-02-3 ]

9-Bromononanoic acid

Similarity: 0.95

Chemical Structure| 2834-05-1

[ 2834-05-1 ]

11-Bromoundecanoic acid

Similarity: 0.95

Bromides

Chemical Structure| 30515-28-7

[ 30515-28-7 ]

7-Bromoheptanoic acid

Similarity: 0.95

Chemical Structure| 2067-33-6

[ 2067-33-6 ]

5-Bromopentanoic acid

Similarity: 0.95

Chemical Structure| 2536-35-8

[ 2536-35-8 ]

16-Bromohexadecanoic acid

Similarity: 0.95

Chemical Structure| 41059-02-3

[ 41059-02-3 ]

9-Bromononanoic acid

Similarity: 0.95

Chemical Structure| 2834-05-1

[ 2834-05-1 ]

11-Bromoundecanoic acid

Similarity: 0.95

Carboxylic Acids

Chemical Structure| 30515-28-7

[ 30515-28-7 ]

7-Bromoheptanoic acid

Similarity: 0.95

Chemical Structure| 2067-33-6

[ 2067-33-6 ]

5-Bromopentanoic acid

Similarity: 0.95

Chemical Structure| 2536-35-8

[ 2536-35-8 ]

16-Bromohexadecanoic acid

Similarity: 0.95

Chemical Structure| 41059-02-3

[ 41059-02-3 ]

9-Bromononanoic acid

Similarity: 0.95

Chemical Structure| 2834-05-1

[ 2834-05-1 ]

11-Bromoundecanoic acid

Similarity: 0.95

; ;