天堂网亚洲,天天操天天搞,91视频高清,菠萝蜜视频在线观看入口,美女视频性感美女视频,95丝袜美女视频国产,超高清美女视频图片

Home Cart 0 Sign in  

[ CAS No. 6344-05-4 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 6344-05-4
Chemical Structure| 6344-05-4
Structure of 6344-05-4 * 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 [ 6344-05-4 ]

Related Doc. of [ 6344-05-4 ]

Alternatived Products of [ 6344-05-4 ]
Product Citations

Product Citations

Prinsloo, Izak F. ; Petzer, Jacobus P. ; Cloete, Theunis T. , et al. DOI: PubMed ID:

Abstract: The small mol., isatin, is a well-known reversible inhibitor of the monoamine oxidase (MAO) enzymes with IC50 values of 12.3 and 4.86μM for MAO-A and MAO-B, resp. While the interaction of isatin with MAO-B has been characterized, only a few studies have explored structure-activity relationships (SARs) of MAO inhibition by isatin analogs. The current study therefore evaluated a series of 14 isatin analogs as in vitro inhibitors of human MAO-A and MAO-B. The results indicated good potency MAO inhibition for some isatin analogs with five compounds exhibiting IC50 < 1μM. 4-Chloroisatin (1b) and 5-bromoisatin (1f) were the most potent inhibitors with IC50 values of 0.812 and 0.125μM for MAO-A and MAO-B, resp. These compounds were also found to be competitive inhibitors of MAO-A and MAO-B with Ki values of 0.311 and 0.033μM, resp. Among the SARs, it was interesting to note that C5-substitution was particularly beneficial for MAO-B inhibition. MAO inhibitors are established drugs for the treatment of neuropsychiatric and neurodegenerative disorders, while potential new roles in prostate cancer and cardiovascular disease are being investigated.

Keywords: competitive ; inhibition ; isatin ; monoamine oxidase ; structure-activity relationship

Purchased from AmBeed: ; ; ; ; ; ; ; ; ; ; ; ; ; ;

Product Details of [ 6344-05-4 ]

CAS No. :6344-05-4 MDL No. :MFCD00129178
Formula : C8H4ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :HSYFISNDMZKGRS-UHFFFAOYSA-N
M.W : 181.58 Pubchem ID :96047
Synonyms :

Calculated chemistry of [ 6344-05-4 ]      Expand+

Physicochemical Properties

Num. heavy atoms : 12
Num. arom. heavy atoms : 6
Fraction Csp3 : 0.0
Num. rotatable bonds : 0
Num. H-bond acceptors : 2.0
Num. H-bond donors : 1.0
Molar Refractivity : 47.17
TPSA : 46.17 ?2

Pharmacokinetics

GI absorption : High
BBB permeant : Yes
P-gp substrate : No
CYP1A2 inhibitor : Yes
CYP2C19 inhibitor : No
CYP2C9 inhibitor : No
CYP2D6 inhibitor : No
CYP3A4 inhibitor : No
Log Kp (skin permeation) : -6.46 cm/s

Lipophilicity

Log Po/w (iLOGP) : 0.81
Log Po/w (XLOGP3) : 1.34
Log Po/w (WLOGP) : 0.9
Log Po/w (MLOGP) : 0.75
Log Po/w (SILICOS-IT) : 2.15
Consensus Log Po/w : 1.19

Druglikeness

Lipinski : 0.0
Ghose : None
Veber : 0.0
Egan : 0.0
Muegge : 1.0
Bioavailability Score : 0.55

Water Solubility

Log S (ESOL) : -2.18
Solubility : 1.2 mg/ml ; 0.00661 mol/l
Class : Soluble
Log S (Ali) : -1.91
Solubility : 2.23 mg/ml ; 0.0123 mol/l
Class : Very soluble
Log S (SILICOS-IT) : -3.39
Solubility : 0.0735 mg/ml ; 0.000405 mol/l
Class : Soluble

Medicinal Chemistry

PAINS : 0.0 alert
Brenk : 1.0 alert
Leadlikeness : 1.0
Synthetic accessibility : 1.6

Safety of [ 6344-05-4 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319 Packing Group:N/A
GHS Pictogram:
Recommend Products
Same Skeleton Products

Technical Information

Historical Records

Related Functional Groups of
[ 6344-05-4 ]

Chlorides

Chemical Structure| 18711-15-4

[ 18711-15-4 ]

4,6-Dichloroisatin

Similarity: 0.98

Chemical Structure| 18711-13-2

[ 18711-13-2 ]

4,7-Dichloroindoline-2,3-dione

Similarity: 0.95

Chemical Structure| 6341-92-0

[ 6341-92-0 ]

6-Coroindoline-2,3-dione

Similarity: 0.91

Chemical Structure| 1677-48-1

[ 1677-48-1 ]

5,6-Dichloroindoline-2,3-dione

Similarity: 0.89

Chemical Structure| 7477-63-6

[ 7477-63-6 ]

7-Cloroindoline-2,3-dione

Similarity: 0.88

Amides

Chemical Structure| 18711-15-4

[ 18711-15-4 ]

4,6-Dichloroisatin

Similarity: 0.98

Chemical Structure| 18711-13-2

[ 18711-13-2 ]

4,7-Dichloroindoline-2,3-dione

Similarity: 0.95

Chemical Structure| 6341-92-0

[ 6341-92-0 ]

6-Coroindoline-2,3-dione

Similarity: 0.91

Chemical Structure| 1677-48-1

[ 1677-48-1 ]

5,6-Dichloroindoline-2,3-dione

Similarity: 0.89

Chemical Structure| 7477-63-6

[ 7477-63-6 ]

7-Cloroindoline-2,3-dione

Similarity: 0.88

Ketones

Chemical Structure| 18711-15-4

[ 18711-15-4 ]

4,6-Dichloroisatin

Similarity: 0.98

Chemical Structure| 18711-13-2

[ 18711-13-2 ]

4,7-Dichloroindoline-2,3-dione

Similarity: 0.95

Chemical Structure| 6341-92-0

[ 6341-92-0 ]

6-Coroindoline-2,3-dione

Similarity: 0.91

Chemical Structure| 1677-48-1

[ 1677-48-1 ]

5,6-Dichloroindoline-2,3-dione

Similarity: 0.89

Chemical Structure| 7477-63-6

[ 7477-63-6 ]

7-Cloroindoline-2,3-dione

Similarity: 0.88

Related Parent Nucleus of
[ 6344-05-4 ]

Indolines

Chemical Structure| 18711-15-4

[ 18711-15-4 ]

4,6-Dichloroisatin

Similarity: 0.98

Chemical Structure| 18711-13-2

[ 18711-13-2 ]

4,7-Dichloroindoline-2,3-dione

Similarity: 0.95

Chemical Structure| 6341-92-0

[ 6341-92-0 ]

6-Coroindoline-2,3-dione

Similarity: 0.91

Chemical Structure| 1677-48-1

[ 1677-48-1 ]

5,6-Dichloroindoline-2,3-dione

Similarity: 0.89

Chemical Structure| 7477-63-6

[ 7477-63-6 ]

7-Cloroindoline-2,3-dione

Similarity: 0.88

; ;