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US3890435A Expired / Lapsed US ⏱️ 0.0 years remaining

Antibiotic substance

Assignee: Imperial Chemical Industries Ltd
•
Filing: 1971-04-07
•
Granted: 1975-06-17
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Expires: 1991-04-07
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Abstract

Abstract The new compound known as cytochalasin E and a process for its manufacture by cultivation of the organism Rosellinia Necatrix. The compound produces effects on tissue culture cells and is useful in the study of cytological processes.

Inventors

  • 👤 Douglas Broadbent
  • 👤 Brian Frederick Burrows
  • 👤 Stephen Barnaby Carter
  • 👤 Harold George Hemming

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 06:55
CPC Classifications
C; C07; C07D; C07D491/00; C07D491/12; C07D491/20; C12; C12N; C12N1/00; C12N1/14; C12N1/145; C12P; C12P1/00; C12P1/02; C12P17/00; C12P17/18; C12P17/188; C12R; C12R2001/00; C12R2001/645; Y; Y10; Y10S; Y10S435/00; Y10S435/8215; Y10S435/911

Claims Analysis

Total Claims: 3
Claim 1
Independent Claim 109 words
THE COMPOUND CYTOCHALASIN E, SAID COMPOUND HAVING THE FOLLOWING CHARACTERISTICS: METLING POINT: VARIABLE BETWEEN 200* AND 200*C., BUT COMMONLY 206*-209*C. INFRA-RED SPECTRUM; BANDS HAVING V MAX (IN LIQUID PARAFFIN) AT 3520,3450,3200,3120 (ALL WEAK),1760,1730,1705 (ALL STRONG), 1670, 1640, (BOTH WEAK) CM.-1 ULTRAVIOLET SPECTRUM: NO SELECTIVE ABSORPTION BETWEEN 225 MU AND 350 MU PROTON MAGNETIC RESONANCE SPECTRUM: PEAKS IN THE REGION OF *=2.8 (AROMATIC PROTONS) WHEN MEASURED IN CDCL3 OR C5D5N; PEAKS (DOUBLETS) CENTRED (WHEN MEASURED IN C5D5N) AT *=3.16 AND *4.10 RESPECTIVELY, BOTH HAVING A COUPLING CONSTANT OF 12.0 CYCLES PER SECOND. MASS SPECTROMETRY: HEAVIEST ION OBSERVED:M/E=495, CORRESPONDING TO C28H33N07 OTHER IONS: M/E=337, CORRESPONDING TO C22H27NO2 M/E=246, CORRESPONDING TO C15H20NO2
Claim 2
Dependent Claim 109 words
THE COMPOUND CYTOCHALASIN E, SAID COMPOUND HAVING THE FOLLOWING CHARACTERISTICS: METLING POINT: VARIABLE BETWEEN 200* AND 200*C., BUT COMMONLY 206*-209*C. INFRA-RED SPECTRUM; BANDS HAVING V MAX (IN LIQUID PARAFFIN) AT 3520,3450,3200,3120 (ALL WEAK),1760,1730,1705 (ALL STRONG), 1670, 1640, (BOTH WEAK) CM.-1 ULTRAVIOLET SPECTRUM: NO SELECTIVE ABSORPTION BETWEEN 225 MU AND 350 MU PROTON MAGNETIC RESONANCE SPECTRUM: PEAKS IN THE REGION OF *=2.8 (AROMATIC PROTONS) WHEN MEASURED IN CDCL3 OR C5D5N; PEAKS (DOUBLETS) CENTRED (WHEN MEASURED IN C5D5N) AT *=3.16 AND *4.10 RESPECTIVELY, BOTH HAVING A COUPLING CONSTANT OF 12.0 CYCLES PER SECOND. MASS SPECTROMETRY: HEAVIEST ION OBSERVED:M/E=495, CORRESPONDING TO C28H33N07 OTHER IONS: M/E=337, CORRESPONDING TO C22H27NO2 M/E=246, CORRESPONDING TO C15H20NO2
Claim 3
Dependent Claim 65 words
A process for the manufacture of cytochalasin E as define in claim 1 which comprises cultivation of the strain of the organism Rosellinia necatrix CMI 108,006 in an aqueous nutrient medium a temperature of 15*-35*C. and for a period of up to 21 to 22 days, separation of the extract into acidic and neutral fractions and isolation of the cytochalasin E from the neutral fraction.

References Cited (Backward Citations)

US3457274A Cited
US3464891A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1978-06-16 1978-12-16 1979-06-17 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1982-06-16 1982-12-16 1983-06-17 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1986-06-16 1986-12-16 1987-06-17 $7700.00 Window Closed / Lapsed

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