Immuno-suppressive agent

Organic compounds -- part of the class 532-570 series – Organic compounds – Carbohydrates or derivatives

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

C07D30932

Patent

active

053808347

ABSTRACT:
An immuno-suppressive agent containing, as an effective component, an, enopyranose derivative of the following formula (I) or its salt: ##STR1## wherein R.sup.1 is a hydrogen atom, alkyl which may be substituted, alkenyl, alkynyl, --OSO.sub.2 R.sup.7, a halogen atom, --OCOR.sup.7, --NHCOR.sup.8, alkoxy, phenyl which may be substituted or a saccharose residue, R.sup.2 is a hydrogen atom or alkyl, R.sup.3 is a hydrogen atom or a halogen atom, R.sup.4 is a hydrogen atom, --COR.sup.9, silyl which may be substituted or alkyl which may be substituted, one of R.sup.5 and R.sup.6 is hydroxyl, alkoxy which may be substituted, a saccharose residue, cycloalkyloxy which may be substituted or --OCOR.sup.10 and the other is a hydrogen atom or alkyl which may be substituted, or R.sup.4 and R.sup.5 together form a single bond, while R.sup.6 is a hydrogen atom or alkyl which may be substituted, each of R.sup.7, R.sup.9 and R.sup.10 is alkyl or phenyl which may be substituted, R.sup.8 is alkyl, phenyl which may be substituted or benzyloxy, X is a hydrogen atom, alkyl which may be substituted, alkenyl which may be substituted, alkynyl which may be substituted, cycloalkyl which may be substituted, phenyl which may be substituted, pyridyl which may be substituted, furanyl which may be substituted, thienyl which may be substituted, formyl, --COR.sup.11, --C(W.sup.1)W.sup.2 R.sup.11 or --SO.sub.2 R.sup.11, R.sup.11 is a chain hydrocarbon group which may be substituted, a monocyclic hydrocarbon group which may be substituted, a polycyclic hydrocarbon group which may be substituted, a monocyclic heterocycle group which may be substituted, or a polycyclic heterocycle group which may be substituted, W.sup.1 is an oxygen atom or a sulfur atom, W.sup.2 is an oxygen atom, a sulfur atom or --NH--, Y is a hydrogen atom, alkyl which may be substituted, alkenyl which may be substituted or alkynyl which may be substituted.

REFERENCES:
patent: 4256646 (1981-03-01), Hernandez et al.
Carbohydrate Research, 60 (1978) pp. C11-12, John S. Brimacombe, et al., "The Stereochemistry of the Reduciton of 1, 6-Anhydro-3, 4-Dideoxy . . . ".
Carbohydrate Research, 114 (1983), pp. 71-82, Fred Shafizadeh, et al., "Additional Reactions of Levoglucosenone."
Carbohydrate Research, 199 (1990), pp. 243-247, Yvonne Gelas-Mialhe, et al., "New Branched-Chain and Aminodeoxys Sugars From . . . "
Carbohydrate Research, 71 (1979), pp. 169-191, Fred Shafizadeh, et al., "Some Reactions to Levoglucosenone."
Helvetica Chimica Acta, vol. 56, Fasc. 5 (1973)--Nr. 180, pp. 1792-1799, "Versuche Zur Synthese Der . . . "
Chem. Ber. 110, (1977), pp. 1994-2004, P. Koll, et al., "Neue Derivate Der 2, 7-Anhydro . . . "
Rad Jugosl.akad.znan.i umjet., Kem. 2, (1983) pp. 133-141, Dusan Miljkovic, et al., "Conformation-Reactivity Relationship in 1,6-Anhydro . . . "
Chemical Abstracts, vol. 71, No. 23, Dec. 8, 1969, p. 421, An-113208h.
Chemical Abstracts, vol. 75, No. 11, Sep. 13, 1971, p. 501, AN-77215e.
Chemical Abstracts, vol. 76, No. 13, Mar. 27, 1972, p. 403, AN-72723e.
Chemical Abstracts, vol. 76, No. 17, Apr. 24, 1972, p. 482, AN-99948u.
Chemical Abstracts, vol. 78, No. 5, Feb. 5, 1973, p. 539, AN-30143b.
Chemical Abstracts, vol. 78, No. 5, Feb. 5, 1973, p. 539, AN-30144c.
Chemical Abstracts, vol. 78, No. 11, Mar. 19, 1973, p. 508, AN-72487x.
Chemical Abstracts, vol. 78, No. 13, Apr. 2, 1973, p. 462, AN-84659t.
Chemical Abstracts, vol. 78, No. 25, Jun. 25, 1973, p. 455, AN-160054j.
Chemical Abstracts, vol. 80, No. 7, Feb. 18, 1974, p. 326, AN-37400h.
Chemical Abstracts, vol. 80, No. 23, Jun. 10, 1974, p. 507, AN 133710e.
Chemical Abstracts, vol. 81, No. 17, Oct. 28, 1974, p. 565, AN-105830w.
Chemical Abstracts, vol. 82, No. 23, Jun. 9, 1975, p. 646, AN-156638t.
Chemical Abstracts, vol. 83, No. 11, Sep. 15, 1975, p. 637, AN-97757b.
Chemical Abstracts, vol. 83, No. 19, Nov. 19, 1975, p. 580, An-164449t.
Chemical Abstracts, vol. 83, No. 23, Dec. 8, 1975, p. 499, AN-193604v.
Chemical Abstracts, vol. 84, No. 19, May 10, 1976, p. 537, AN-135994g.
Chemical Abstracts, vol. 84, No. 23, Jun. 7, 1976, p. 503, AN-165150w.
Chemical Abstracts, vol. 86, No. 11, Mar. 14, 1977, p. 653, AN-73024w.
Chemical Abstracts, vol. 87, No. 25, Dec. 19, 1977, p. 670, AN-200858u.
Chemical Abstracts, vol. 88, No. 9, Feb. 27, 1978, p. 405, AN 62540b.
Chemical Abstracts, vol. 88, No. 25, Jun. 19, 1978, p. 736, AN-190528r.
Chemical Abstracts, vol. 90, No. 5, Jan. 29, 1979, p. 513, AN-39142f.
Chemical Abstracts, vol. 90, No. 16, Apr. 16, 1979, p. 640, AN-131093p.
Chemical Abstracts, vol. 90, No. 17, Apr. 23, 1979, AN-138118.
Chemical Abstracts, vol. 92, No. 9, Mar. 3, 1980, p. 718, AN-76872f.
Chemical Abstracts, vol. 93, No. 13, Sep. 29, 1980, p. 692, AN-132748e.
Chemical Abstracts, vol. 93, No. 21, Nov. 24, 1980, p. 721, AN-204964x.
Chemical Abstracts, vol. 94, No. 17, Apr. 27, 1981, p. 792, AN-140064q.
Chemical Abstracts, vol. 95, No. 3, Jul. 20, 1981, p. 735, AN-25408p.
Chemical Abstracts, vol. 96, No. 7, Feb. 15, 1982, p. 650, AN-52606d.
Chemical Abstracts, vol. 96, No. 13, Mar. 29, 1982, p. 675, AN-103915p.
Chemical Abstracts, vol. 96, No. 23, Jun. 7, 1982, p. 711, AN-200057t.
Chemical Abstracts, vol. 97, No. 5, Aug. 2, 1982, p. 607, AN-39251k.
Chemical Abstracts, vol. 97, No. 17, Oct. 25, 1982, p. 724, AN-145197g.
Chemical Abstracts, vol. 102, No. 9, Mar. 4, 1985, p. 636, AN-79260r.
Chemical Abstracts, vol. 102, No. 13, Apr. 1, 1985, p. 677, AN-113128r.
Chemical Abstracts, vol. 103, No. 23, Dec. 9, 1985, p. 705, AN-196330v.
Chemical Abstracts, vol. 105, No. 13, Sep. 29, 1986, p. 708, AN-115324n.
Chemical Abstracts, vol. 107, No. 5, Aug. 3, 1987, p. 736, AN-40142g.
Chemical Abstracts, vol. 107, No. 11, Sep. 14, 1987, p. 718, AN-96980w.
Chemical Abstracts, vol. 107, No. 19, Nov. 9, 1987, p. 693, AN-175734x.
Chemical Abstracts, vol. 108, No. 7, Feb. 15, 1988, p. 763, AN-56455t.
Chemical Abstracts, vol. 108, No. 15, Apr. 11, 1988, p. 795, AN-132188a.
Chemical Abstracts, vol. 108, No. 19, May 9, 1988, p. 687, AN-167814d.
Chemical Abstracts, vol. 109, No. 7, Aug. 15, 1988, p. 662, AN-54555x.
Chemical Abstracts, vol. 109, No. 21, Nov. 21, 1988, p. 746, AN-190680m.
Chemical Abstracts, vol. 110, No. 5, Jan. 30, 1989, p. 574, AN-39256c.
Chemical Abstracts, vol. 110, No. 23, Jun. 5, 1989, p. 787, AN-213189v.
Chemical Abstracts, vol. 111, No. 7, Aug. 14, 1989, p. 803, AN-58188u.
Chemical Abstracts, vol. 112, No. 19, May 7, 1990, p. 728, AN-178563e.
Chemical Abstracts, vol. 113, No. 13, Sep. 24, 1990, p. 734, AN-115700x.
Chemical Abstracts, vol. 115, No. 7, Aug. 19, 1991, p. 845.
Chemical Abstracts, vol. 86, No. 21, May 23, 1977, p. 498, AN-155908b.
Chemical Abstracts, vol. 91, No. 17, Oct. 22, 1979, p. 619, AN-140416u.
Chemical Abstracts, vol. 93, No. 4, Aug. 4, 1980, p. 871, AN-46059x.

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Immuno-suppressive agent does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Immuno-suppressive agent, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Immuno-suppressive agent will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-851546

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.