Biogenese des derives diguanidiques chez la sangsue, Hirudo medicinalis L.—I. Origine des groupements guanidiques et de la chaine carbonee

Audit, C. O.; Viala, B.; Robin, Y

doi:10.1016/0010-406x(67)90770-0

Cited by 11 publications

(2 citation statements)

References 23 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…In this case there are eight protons from the amine and two from H SO for hydrogen bonding per molecule, out of which eight of molecule I and nine of molecules II and III are involved N-H2O type of hydrogen bonding (6). The crystal structure of arcaine sulfate is given in Scheme 1.…”

Section: Crystal Structurementioning

confidence: 98%

FT-IR, Raman, and SERS Spectra of Arcaine Sulfate

Eapen¹,

Joe²,

Aruldhas

1997

Journal of Solid State Chemistry

View full text Add to dashboard Cite

Section: Crystal Structurementioning

confidence: 98%

FT-IR, Raman, and SERS Spectra of Arcaine Sulfate

Eapen¹,

Joe²,

Aruldhas

1997

Journal of Solid State Chemistry

View full text Add to dashboard Cite

“…This new base, N -formamidino-N'-(3-aminopropyl)-1,4-diaminobutane, or guanylspermidine (170), has been previously isolated from leeches and marine worms together with its related putrescine and cadaverine analogues (379)(380)(381)(382)(383)(384)(385)(386)(387)(388)(389). This new base, N -formamidino-N'-(3-aminopropyl)-1,4-diaminobutane, or guanylspermidine (170), has been previously isolated from leeches and marine worms together with its related putrescine and cadaverine analogues (379)(380)(381)(382)(383)(384)(385)(386)(387)(388)(389).…”

Section: Macrocyclic Lactone Antibioticsmentioning

confidence: 99%