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39156-67-7

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39156-67-7 Usage

Description

Dihydrocytochalasin B is a white powder with significant biological activities, primarily known for its effects on cell morphology and motility. It acts as an inducer, influencing the structural and functional aspects of cells.

Uses

Used in Pharmaceutical Industry:
Dihydrocytochalasin B is used as a pharmaceutical agent for its ability to alter cell morphology and motility. It is particularly valuable in research and development for understanding cellular processes and potentially in the treatment of conditions related to cell movement and structure.
Used in Research Applications:
In the field of biological and medical research, Dihydrocytochalasin B is used as a research tool to study the effects of various factors on cell shape, movement, and overall function. Its use in laboratories helps scientists gain insights into cellular mechanisms and develop targeted therapies for various diseases.
Used in Drug Development:
Dihydrocytochalasin B is also utilized in the development of new drugs, particularly those aimed at targeting cell motility and morphology. Its unique properties make it a valuable compound in the creation of novel therapeutics for a range of conditions, including cancer and other diseases characterized by abnormal cell behavior.

Check Digit Verification of cas no

The CAS Registry Mumber 39156-67-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,9,1,5 and 6 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 39156-67:
(7*3)+(6*9)+(5*1)+(4*5)+(3*6)+(2*6)+(1*7)=137
137 % 10 = 7
So 39156-67-7 is a valid CAS Registry Number.
InChI:InChI=1/C29H39NO5/c1-18-9-7-13-22(31)15-16-25(32)35-29-23(14-8-10-18)27(33)20(3)19(2)26(29)24(30-28(29)34)17-21-11-5-4-6-12-21/h4-6,8,11-12,14,18-19,22-24,26-27,31,33H,3,7,9-10,13,15-17H2,1-2H3,(H,30,34)/b14-8+/t18-,19-,22+,23-,24-,26+,27+,29-/m0/s1

39156-67-7Relevant articles and documents

CYTOCHALASINS: STRUCTURE-ACTIVITY RELATIONSHIPS

Bottalico, Antonio,Capasso, Renato,Evidente, Antonio,Randazzo, Giacomino,Vurro, Maurizio

, p. 93 - 96 (2007/10/02)

Seven cytochalasins, 7-O-acetylcytochalasin A and two derivatives of cytochalasin B were assayed for Pseudomonas syringae, Bacillus megaterium, and for Geotrichum candidum.Their ability to inhibit the growth of tomato seedlings and their toxicity to brine shrimp (percent larvae mortality) were also investigated.Among the compounds assayed only cytochalasin A showed antibiotic and fungicidal activity.Toxicity to tomato seedlings was exhibited by both - and -macrocyclic cytochalasins, while the activity decreased in the derivatives acetylated on the 7-hydroxy groupand markedly in cytochalasin E.In the brine shrimp bioassay, cytochalasin E was the most active mycotoxin, but generally, at low concentrations, the cytochalasins with the -macrocyclic ring were more active than those with the -macrocyclic ring; cytochalasin A appeared to be the most toxic.

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