107021-10-3 Usage
Molecular Structure
Tetracyclic ring system The compound has a unique four-ring structure, which contributes to its complexity and potential applications.
Stereochemistry
(1S,3S,5Z,7R,8E,11S,12S,13E,15S,17R,21R,23R,25S) This indicates the specific arrangement of atoms in the molecule, which is crucial for its properties and potential applications.
Functional Groups
Multiple hydroxyl (-OH) and carbonyl (C=O) groups The presence of these groups contributes to the compound's reactivity and potential for further chemical reactions.
Double Bonds
2,4-Octadienoic acid has two double bonds (Dienes) in its structure, which can participate in various chemical reactions and contribute to its properties.
Methoxy and Oxoethylidene Groups
5,13-bis(2-methoxy-2-oxoethylidene) These functional groups add complexity to the molecule and can be involved in various chemical reactions.
Oxo (keto) Group
19-oxo This carbonyl group is part of the compound's structure and can participate in chemical reactions.
Applications
Pharmaceutical, organic synthesis, and chemical research Due to its complex and diverse structure, this compound has potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 107021-10-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,7,0,2 and 1 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 107021-10:
(8*1)+(7*0)+(6*7)+(5*0)+(4*2)+(3*1)+(2*1)+(1*0)=63
63 % 10 = 3
So 107021-10-3 is a valid CAS Registry Number.
107021-10-3Relevant articles and documents
Isolation and Structure of Bryostatins 12 and 13
Pettit, George R.,Leet, John E.,Herald, Cherry L.,Kamano, Yoshiaki,Boettner, Fred E.
, p. 2854 - 2860 (1987)
Bryostatins 12 (4, 3.7 mg) and 13 (5, 0.7 mg) were isolated from ca. 1000 kg of the marine bryozoan Bugula neritina (Linnaeus) found in the Eastern Pacific Ocean (California).The new bryostatins led to strong cell growth inhibitory (PS cell line ED50 0.014 and 0.0054 μg/mL) and antineoplastic activity (for bryostatin 12, a 47-68percent increase in life extension at 30-50 μg/kg) against the marine P388 lymphocytic leukemia (PS system).In addition to the previously known constituents (bryostatin 1-3) of Bugula neritina from this ocean area the presence of bryostatins 8(13.2 mg) and 9(16.4 mg) was also established.A detailed series of 1H-1H COSY, 2D-J-resolved, 1H-13C 2D-shift correlated, and 1H- NOE difference 1H NMR experiments combined with 13C NMR and SP-SIMS studies were employed to elucidate the structures of bryostatins 12 and 13.
