752251-07-3

Basic information

• Product Name: H-L-Thr(OBn)-D-Ser(OBn)-LSer(OBn)-(3S)-THQ(OBn)
• Synonyms: H-L-Thr(OBn)-D-Ser(OBn)-LSer(OBn)-(3S)-THQ(OBn)
• CAS NO: 752251-07-3
• Molecular Weight: 935.153
• Mol File: 752251-07-3.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: H-L-Thr(OBn)-D-Ser(OBn)-LSer(OBn)-(3S)-THQ(OBn)(CAS DataBase Reference)
• NIST Chemistry Reference: H-L-Thr(OBn)-D-Ser(OBn)-LSer(OBn)-(3S)-THQ(OBn)(752251-07-3)
• EPA Substance Registry System: H-L-Thr(OBn)-D-Ser(OBn)-LSer(OBn)-(3S)-THQ(OBn)(752251-07-3)

Safety Data

• Hazardous Substances Data: 752251-07-3(Hazardous Substances Data)

Upstream product

• 752251-04-0 (S,S)-{2-benzyloxy-1-[1-(3,4-dihydroxy-benzyl)-2-dimethylamino-ethylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester 
• 752251-20-0 (2R)-3-benzyloxy-2-((2S)-3-benzyloxy-2-tert-butoxycarbonylamino-butyrylamino)propionic acid 
• 752251-21-1 (2R)-3-benzyloxy-2-((2S)-3-benzyloxy-2-tert-butoxycarbonylamino-butyrylamino)propionic acid methyl ester 
• 752251-02-8 (S)-[2-(3,4-dihydroxy-phenyl)-1-dimethylcarbamoyl-ethyl]-carbamic acid tert-butyl ester 
• 15260-10-3 N-Boc-O-benzyl-L-threonine 
• 59-92-7 levodopa 
• 752251-06-2 (S)-3-amino-6,7-bis(OBn)-1,1-dimethyl-1,2,3,4-tetrahydroquinolin-1-ium L-ser(OBn)-D-ser (OBn)-BocL-thr(OBn) 
• 752251-05-1 (2S,3S)-6,7-bis-benzyloxy-3-(3-benzyloxy-2-tert-butoxycarbonylaminopropionylamino)-1,1-dimethyl-1,2,3,4-tetrahydroquinolinium 
• 752251-19-7 (S)-3-((S)-2-Amino-3-benzyloxy-propionylamino)-6,7-bis-benzyloxy-1,1-dimethyl-1,2,3,4-tetrahydro-quinolinium 
• 752251-00-6 (2S,3S)-3-(3-benzyloxy-2-tert-butoxycarbonylamino-propionylamino)-6,7-dihydroxy-1,1-dimethyl-1,2,3,4-tetrahydro-quinolinium 
• 862695-37-2 4-((S)-2-Amino-3-dimethylamino-propyl)-benzene-1,2-diol 
• 67389-47-3 (R)-3-benzyloxy-2-tert-butoxycarbonyl-amino-propionic acid methyl ester 
• 84907-81-3 (2R)-3-benzyloxy-2-aminopropanoic acid methyl ester 

Relevant articles and documents

Allelopathic Activity of the Iron Chelator Anachelin?–?A Molecular Hybrid with a Dual Mode of Action

One of the compounds suggested to be responsible for the cyanobacterial dominance over competing green algae is identified. Evidence is provided on the molecular, chemical level that the iron chelator anachelin from the cyanobacterium Anabaena cylindrica promotes both the growth of cyanobacteria and reduces the growth of competing chlorophytes. These results illustrate a molecular strategy of addressing two challenges (nutrient availability and algal competition) by one molecule. Such strategies could be implied in harmful algal blooms in marine and freshwater environments.