AR015621A1 - DERIVATIVES OF 1-THIOGALACTOSE, PHARMACEUTICAL COMPOSITION, TREATMENT METHODS AND SUPPORT CONTAINING SUCH DERIVATIVES - Google Patents

DERIVATIVES OF 1-THIOGALACTOSE, PHARMACEUTICAL COMPOSITION, TREATMENT METHODS AND SUPPORT CONTAINING SUCH DERIVATIVES

Info

Publication number
AR015621A1
AR015621A1 ARP980102031A ARP980102031A AR015621A1 AR 015621 A1 AR015621 A1 AR 015621A1 AR P980102031 A ARP980102031 A AR P980102031A AR P980102031 A ARP980102031 A AR P980102031A AR 015621 A1 AR015621 A1 AR 015621A1
Authority
AR
Argentina
Prior art keywords
group
alkyl
cycloalkenyl
derivatives
hydrogen
Prior art date
Application number
ARP980102031A
Other languages
Spanish (es)
Original Assignee
Synsorb Biotech Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority claimed from US08/970,384 external-priority patent/US5968907A/en
Application filed by Synsorb Biotech Inc filed Critical Synsorb Biotech Inc
Publication of AR015621A1 publication Critical patent/AR015621A1/en

Links

Classifications

    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

Landscapes

  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Derivados de 1-tiogalactosa que inhiben el enlace de toxinas, como enterotoxina lábil por calor o toxina de colera, a sus receptores, ya sea in vitro o invivo de la formula (I) en donde: R1 es seleccionado del grupo que consiste de hidrogeno, alquilo, alquilo sustituido, alquenilo, alcarilo, alcoxialquilo,arilo, ciclalquilo, cicloalquenilo, heteroarilo, heterocíclico y tioalcoxialquilo,; R2 es seleccionado del grupo que consiste de hidrogeno, alquilo, alquilosustituido, alquenilo, alcarilo, alcoxialquilo, arilo, cicloalquilo, cicloalquenilo, heteroarilo, heterocíclico y tioalcoxialquilo; R3 es seleccionado delgrupo que consiste en hidrogeno, alquilo, alquilo sustituido, alquenilo, alcarilo, alcoxialquilo, arilo, cicloalquilo, cicloalquenilo, heteroarilo,heterocíclico y tioalcoxialquilo; o R1 y R2 o R1 y R3, o R2 y R3 o R1 R2 y R3 se pueden unir, junto con los átomos de carbono a los cuales R1 y/o R2 y/o R3están adheridos, para formar un anillo heterocíclico, cicloalquilo o cicloalquenilo; R4 es seleccionado del grupo que consiste de -XR5, -XC(W)R6, -XC(W)XR7, y-C(W)XR8; en donde W es seleccionado del grupo que consiste de oxígeno, azufre y NH; y X y X son cada uno independientemente seleccionados del grupo queconsiste de oxígeno,azufre y -NR9-, en donde R9 es seleccionado del grupo que consiste de hidrogeno y alquilo; o cuando R4 es -XR5 y R5 no es hidrogeno, Xpuede ser además seleccionado del grupo que consiste de -S(O)- y -SO2; R5 es seleccionado del grupo que consiste dehidrogeno, alquilo, alquenilo, alcarilo,alcoxialquilo, arilo, cicloalquilo, cicloalquenilo, heteroarilo, heterocíclico y tioalcoxialquilo, y cuando X es -NR9-, entonces R9 junto con X pueden formarun aminoácido o R5 y R1 o R5 y R2, o R5 y R3 se pueden unir junto con X del grupo -XR5 y los átomos de carbono a los cuales R1 y/o R2 y/o R3 están adheridos,para formar un anillo heterocíclico; R6 es seleccionado del grupo que consiste de alquilo, alquenilo, alcarilo, alcoxialquilo, arilo, cicloalquilo,cicloalquenilo, heteroarilo, heterocíclico y tioalcoxialquilo; o R6 y R1, o R6 y R2, o R6 y R3 se pueden unir, junto con la porcion -XC(W)- del grupo -XC(W)R61-Thiogalactose derivatives that inhibit the binding of toxins, such as heat labile enterotoxin or cholera toxin, to their receptors, either in vitro or invivo of formula (I) where: R1 is selected from the group consisting of hydrogen , alkyl, substituted alkyl, alkenyl, alkaryl, alkoxyalkyl, aryl, cyclolalkyl, cycloalkenyl, heteroaryl, heterocyclic and thioalkoxyalkyl; R2 is selected from the group consisting of hydrogen, alkyl, substituted alkyls, alkenyl, alkaryl, alkoxyalkyl, aryl, cycloalkyl, cycloalkenyl, heteroaryl, heterocyclic and thioalkoxyalkyl; R3 is selected from the group consisting of hydrogen, alkyl, substituted alkyl, alkenyl, alkaryl, alkoxyalkyl, aryl, cycloalkyl, cycloalkenyl, heteroaryl, heterocyclic and thioalkoxyalkyl; or R1 and R2 or R1 and R3, or R2 and R3 or R1 R2 and R3 can be attached, together with the carbon atoms to which R1 and / or R2 and / or R3 are attached, to form a heterocyclic ring, cycloalkyl or cycloalkenyl; R4 is selected from the group consisting of -XR5, -XC (W) R6, -XC (W) XR7, and-C (W) XR8; wherein W is selected from the group consisting of oxygen, sulfur and NH; and X and X are each independently selected from the group consisting of oxygen, sulfur and -NR9-, wherein R9 is selected from the group consisting of hydrogen and alkyl; or when R4 is -XR5 and R5 is not hydrogen, X can also be selected from the group consisting of -S (O) - and -SO2; R5 is selected from the group consisting of hydrogen, alkyl, alkenyl, alkaryl, alkoxyalkyl, aryl, cycloalkyl, cycloalkenyl, heteroaryl, heterocyclic and thioalkoxyalkyl, and when X is -NR9-, then R9 together with X can form an amino acid or R5 and R1 or R5 and R2, or R5 and R3 can be joined together with X of the group -XR5 and the carbon atoms to which R1 and / or R2 and / or R3 are attached, to form a heterocyclic ring; R6 is selected from the group consisting of alkyl, alkenyl, alkaryl, alkoxyalkyl, aryl, cycloalkyl, cycloalkenyl, heteroaryl, heterocyclic and thioalkoxyalkyl; or R6 and R1, or R6 and R2, or R6 and R3 can be joined, together with the -XC (W) - portion of the group -XC (W) R6

ARP980102031A 1997-11-14 1998-04-30 DERIVATIVES OF 1-THIOGALACTOSE, PHARMACEUTICAL COMPOSITION, TREATMENT METHODS AND SUPPORT CONTAINING SUCH DERIVATIVES AR015621A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/970,384 US5968907A (en) 1996-11-14 1997-11-14 1-thiogalactose derivatives

Publications (1)

Publication Number Publication Date
AR015621A1 true AR015621A1 (en) 2001-05-16

Family

ID=25516875

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP980102031A AR015621A1 (en) 1997-11-14 1998-04-30 DERIVATIVES OF 1-THIOGALACTOSE, PHARMACEUTICAL COMPOSITION, TREATMENT METHODS AND SUPPORT CONTAINING SUCH DERIVATIVES

Country Status (3)

Country Link
AR (1) AR015621A1 (en)
TW (1) TW467917B (en)
ZA (1) ZA983692B (en)

Also Published As

Publication number Publication date
ZA983692B (en) 1998-11-11
TW467917B (en) 2001-12-11

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