chemotherapeutic agents / antibiotics, chapter 34-39

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hemotherapeutic Agents / Antibiotics, chapter 34-3 Antibacterial compounds (procaryotes) Antiparasitic agents (eucarytotes) - Chap Antifungal compounds (eucarytotes) Antiviral compounds Anticancer compounds Protozoa Helmints Insects (Scabies lice etc.) (Fungi chapt. 36)

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Page 1: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Chemotherapeutic Agents / Antibiotics, chapter 34-39

•Antibacterial compounds (procaryotes)•Antiparasitic agents (eucarytotes) - Chapt 35•Antifungal compounds (eucarytotes)•Antiviral compounds•Anticancer compounds

ProtozoaHelmintsInsects (Scabies lice etc.)

(Fungi chapt. 36)

Page 2: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Protozoa

Eucaryotes, unicellular (may exist in colonies)Protozoa and algae (protocista)Complex replication (sexual and asexual) Patogenic P. most common tropical area3. world diseasesMany diseases can be prevented by clean drinking waterCertain protozal diseases spread by insects

Ex. patogenic protozoa

ÿ Trichomonas vaginalis: Gelital infections

ÿ Giardia lamblia: Diarea

ÿ Toxoplasma gondii : Toksoplasmosis

ÿ Trypanozomas sp: Sleeping sickness

ÿ Entamoeba histolytica: Dysentery

ÿ Plasmodium sp: Malaria

ÿ Pneumocystis carinii : Oportunistic, AIDS

Page 3: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Treatment of diseases caused by amebia, giardia, trichomonas

MetronidazolFlagyl®, Metronidazol®

N

N

OH

CH3

O2

NAlso effective against anaerobic bacteriaProbably pro-drug -reductive activation(mech. not fully understood)

N

N

OH

CH3O2N

Anaerobe org.e-

N

N

OH

CH3O2N

O2O O

HO-OH

2 HO

MetabolN

N

OH

O2NOH N

N

OH

O2NOH

O

Active metabol.

Phase II conjugation

OH

NH

OH

O

H2N

O CH3

O

N

N

OH

CH3O2N

Formation of toxic reactive oxygen species

Related comp.treatment of African sleeping sickness

OO2NN

NSO2

Page 4: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Anti - Malaria drugsPlasmodium sp. Vektor: Anopheles moskito. Complex life cyclus.

De fleste l.m.aktive her

Mal aria = bad air

40% of world population at risk300 mil acute illnessess pr yearca 1 mill deaths pr yearMalaria kills a child every 30 sec.90% in incidents sub-sahara Africa

Page 5: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Historic drugs-Azodyes and salvarsan (1. synthetic effective drug)-Quinine fra Cinchona (Kinabark)

Cinchona pubescens (Kinatre) from South America

N

MeO

HON

QuinineN

Quinoline

MOdern antimalarials

Azo dyes Bayer etcLate 1800-century, ex.

NN N

HO3S

Metylorange

NN

O2N

Pararødt

HO

Salvarsan1. antisyphilis drug 1912

AsAs

HOOH

NH2

H2N

Screening of dyes as antibacterials

NN NH2

SO

OH2N

H2N

1932: Prontocil active against Streptoccocces infectionno activity on bacterial cultures

1935: Prontocil metabilized (azoreductase) to Sulfanilamid in vivo

NH2SO

OH2N (rel. toxisk)

Modern sulfa drugsr

NH2SO

OHNR

R: Aryl or hetroaryl

Page 6: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Quinolines

QuinineKinin®

N

MeO

HO

N MeflokinLariam®

N

CF3

CF3

HO

N

H

KlorokinKlorokinfosfat®

N

NH

Cl

N

HydroksyklorokinPlaquenil®

N

NH

Cl

N

HO

More active, less tox (comp Quinine)Resistance!

Also klorokin resistantP. palsifarum

N

NH

Cl

N

klorokin

N

NH

H3CO

N

Pamakin, 1926

Dye

Quinine

Mechanism

(DNA Intercalation)

Ferriprotoporphyrin IX: Binds to FPIX (metabolite from hemoglobine);tox. form of FPIX, proteinbound FPIX less tox.)

Weak base Hypothesis: Increase pH in parasite

Page 7: Chemotherapeutic Agents / Antibiotics, chapter 34-39

BiguanidesProguanil (= Chloroguanide)Paludrine®Malarone® + atovakvon

Pro-drugInhib. protozoan folate reduktase(c.f. Trimetoprim)

H2

N

O

OH

PABA

H2

N S

O

O

NH

R

Antibakt sulfonamid

N

N N

H

N

OH

H2

N

N

H

OH

O

Dehydropteridinsyre

N

N N

H

N

OH

H2

N

N

H

NH

O

Dehydrofolinsyre

CO2

H

CO2

H

N

N N

N

OH

H2

N

N

H

NH

O

F olinsyre

CO2

H

CO2

H

Fra folinsyre i kosten

hos mennesker

N

N N

H

H

N

OH

H2

N

N

H

NH

O

Tetrahydrofolinsyre

CO2

H

CO2

H

Folat-

reduktase

Essensielle prossesser

hos bakterier og dyr

Inkl tymidinsyntese

Trimetoprim

N

N

NH2

H2

N OCH3

OCH3

OCH3

NH2

enamine

NH

Imine

taut.

OH

enol

O

keto

taut.

Cl

NH

NH

NH

NH NH

Proguanil (chloroguanide)

Liver

N N

NH2N NH2

Cl

1

1

2

2

3

3

4

4

5

5

6

6

Cycloguanil

- H2

Cl

NH

NH

N

NH NH

N

H

N

H

H

N

NH

N

H

NH

Cl

NH

H

N

H

N

NH

Cl

Other biguanidesKlorhexidine

Page 8: Chemotherapeutic Agents / Antibiotics, chapter 34-39

AtovakvonMalarone® + proguanil.Also other parasites (P. carinii)Ubiquinone antimetabolite?

Artemeter og LumefandrinRiamet®

Others

O

O H

H

OO

H

Artemisinfrom Artemisia annuaChinesee trad. med.

O

O

O H

H

OO

H

MeO

Artemeter

Semisynth. analogImproved solubil.

Mech. involves radicals

No cross resist.

Synth. analogs, active field

O

O

Cl

OH

O

OCH3

H3CO

H3CO8 Red

oxUbiquinone, Q10, Cenzyme Qelectron carriercellular respiration

OH

OHCH3

H3CO

H3CO

R

Page 9: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Drugs for Helmint infectionsEukaryotes – Invertebrates. Tropical diseases! Animal parasites; ex Trichinella spiralis (trikiner).

MebendazolVermox®

N

H

N

NH

O

O

OMe

BenzimidazolesMany active analogs knownBinds to tubulin - prevents formation of microtubulesinhib. mitosis (c.f. certain anticancer drugs)May also inhib. fumarate reductase

Page 10: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Drugs against Ectoparasites (insects)

Lice, scabies etc

Permetrin

Nix®

PyretrinesInsecticides from Crysantemum sp

R

OO

R'∗

Cl

Cl∗

OO

O

Synth. analog, more stabileMixt. of 4 stereoisomers

ClCl

ClCl

ClCl

Chlorinated pesticides:LindaneBlock GABA CNS neurtransmittor(Also neurotox. effects on humans)

Page 11: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Irreversible InhibitorsAcetylcholine esterase

Not drugs, nerve gasses, insecticides etc.

LP

O

OR

R2

OH O POH

L

OR

R1O

HOP

O

OR

R1

AgingO P

OH

R1O

Pralidoxim

N

N

OH

Me

OH

Pralidoximmotgift

N

N

O

Me

PO OR

R1

Gen structur mustard gasses

PO

O

N

N

Tabun

FP

O

O

Sarin

LP

O

R1

R2

L: Leaving groupR1: alkoksyR2: alkyl, alkoksy, amino

O

O

O

O

S PS

O

O

Malation

only insects

O

O

O

O

S PO

O

O

Malaoxon

Act as mustard gassesnot tox.

Malation Prioderm® lice

Page 12: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Chemotherapeutic Agents / Antibiotics, chapter 34-39

•Antibacterial compounds (procaryotes)•Antiparasitic agents (eucarytotes) -•Antifungal compounds (eucarytotes) - Chapt 36•Antiviral compounds•Anticancer compounds

Fungicides / Fungistatika / AntimykotikaChemotherapeutics / Antibiotics

Page 13: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Synthetic Antifungals

AzolesN

H

Azol / Pyrrol

N

N

H

1,2-Diazol

N

N

H

1,3-Diazol / Imidazol

N

N

N

H

1,2,4-Triazol

Component of fungus cell walls

Squalen

Squalen epoksidase

O

Squalen epoksid-syklase

HOLanosterol

Lanosterol14a-demetylase

Antimycotic azoles

HOErgosterol

HO

H

H

HO

KolesterolH

H

H

Antimycotic allylic amines

Page 14: Chemotherapeutic Agents / Antibiotics, chapter 34-39

HO

Lanosterol

H

CH3

FeO

NN N

N

14a-demethylase heme(CYP450 fungi)

HOH

CH2OH

HOH

C(OH)3

HCO2H

HOH

FeNN N

N

NN R Antimyc. azole

Page 15: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Klotrimazol: Canesten®, Klotrimazol® utvortesCanesten®, vaginal behandlig

N

N

Cl

Ekonazol: Pevaryl®, utvortesPevaryl®, vaginal behandlig

Miconazol: Daktar®, utvortesDaktar®, vaginal behandlig

N

N

O

Cl

Cl

X

Cl

X=H: Ekonazol

X=Cl: Mikonazol

Ketokonazol:

N

N

Cl

Cl

O

O

O N N

O

"cis", [±]

Itrakonazol:

N

N

N

Cl

Cl

O

O

O N N N

N

N

O

Flukonazol(Racemate)

Vorikonazol

N

N

N

F

F

OH

N

N

F(s)

(R)

SAR:

-Weakly basic azole ring, imidazol / 1,2,4-triazol

(less tox. humans), pKa 6.5-6.8

-2 or 3 other aromatic rings

-Cl (or F) on at least one aromatic ring

(F i flukonazol)

-Lipophilic structures (as lanosterol)

Page 16: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Allylic amines

TerbinafinLamicil®

N

Squalen

Squalen epoksidase

O

Squalen epoksid-syklase

HOLanosterol

Lanosterol14a-demetylase

Antimycotic azoles

HOErgosterol

HO

H

H

HO

KolesterolH

H

H

Antimycotic allylic amines

Prevents formation of cell wall comp.Accumulation of toxic squalene

O

HO LanosterolH

Squaleneepoxidase

Enzyme-Nu

H

HOH

H

Enz--Nu

H

Squalene epoxide cyclase

(AnimalsFungi)

H

B

Page 17: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Antimycotic AntibioticsPolyenes

Proad spectrum. Some effect on certain protozoa. Isolated, Streptomyces sp.Binds to sterols in fungal cell membrane; cell leaks K+, small org. molecules

SAR:•Macrolaktone [26 eor 38-ring, Larger than macrolides ( erytromycin etc)]•Polyene (Macrolides not polyenes)•Several OH-groups•amino sugar, mykosamin•Bad water sol.

O

OO Aminosukker

n

OHn

O

O

OOH

CO2H

OH

HO

OH

HOHOHOOHO

O

OHNH2

OHNystatin AO

O

O

HOO

O

NHO

Erytromycin

HOHO

O

OO

OH

Page 18: Chemotherapeutic Agents / Antibiotics, chapter 34-39

O

O

O

OH

CO2

H

OH

HOOHHOO

HO

O

OH

NH2

OHAmfotericin B

HO

OH

O

O

O

OH

CO2

H

OH

HO

OH

HOHOHOOHO

O

OH

NH2

OHNystatin A

Nystatin Atoxic, bad oral avail; Local treatment, mouth, GI tract

Amfotericin BSysthemic infect (infusion)Somewhat less tox.

O

O

OH

CO2

H

OH

O

OH

NH2

OH

Amfotær struktur

O

O

OH

CO2

OH

O

OH

NH3

OH

O

HO

CO2

H

OH

O

OH

NH2

OH

O

Hemiacetal

O

O

OH

CO2

H

OH

O

OH

NH2

OH

Page 19: Chemotherapeutic Agents / Antibiotics, chapter 34-39

PeptidesCaspofunginSerious systhemic infect.Semisynth. from prod. of fermentation ( Glarea lozoyensis)Inhib. synth of -1,3-D-glucan; cell wall comp. certain fungi

Few good inhib. of fungi cell wall comp. compared to antibacterials

Page 20: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Chemotherapeutic Agents / Antibiotics, chapter 34-39

•Antibacterial compounds (procaryotes)-Antimycobacterials chapt. 37•Antiparasitic agents (eucarytotes) •Antifungal compounds (eucarytotes) •Antiviral compounds•Anticancer compounds

G+ G- Mycobacteria

Page 21: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Pathogenic mycobacteria:M. tuberculosis (tuberculosis)M. Leprae (Leprosy)M. Avium (Opportunistic infection in AIDS patients)M. bovis (mainly cattle infect, infected milk USA)

TUBERCULOSIS (TB)High lipid / wax content in cell wall (mycolic acid)Slow growing organismsAerobe bacteriaResistant to chemicals and dryingEasily killed by heat

Until ca. 1950; 50 % of all infected died

Infection by inhalation of the bacteria

Pulmonary TB most common

May also attack other organs including CNS

30 million people will die from TB the next 10 years

8 million new cases each year

ca. 1/3 of the world population are infected (incl. dormant infections)

ca. 95% of the cases in developing countries

no new drugs on the marked for the last 25 - 30 years

WHO (1993): TB a "global emergency"

Page 22: Chemotherapeutic Agents / Antibiotics, chapter 34-39

HOO

NHMeHO

HOHO

O

HOOH

OH

HN

NH

NHH2N

NHH2N

Inhibits protein synthesisToxic!

First effective drug: Streptomycin 1946

Treatment•Long time ≥6 mnds•Combination of drugs Different stages of bacterial growth

DOT: Directly observed therapy

Page 23: Chemotherapeutic Agents / Antibiotics, chapter 34-39

First-line drugs

IsoniazidIsoniazid®

N

O NHNH2

N

O

NH2

NADH co-enzymein enzyme involved in cell wallcomponent synth

H H

NO

HN NH2

IsoniazideAntituberculosis drug

NO

Mn2+ /O

Active acyl radical formed in vivo

N

O

NH2

HO

N

Inactive der. of co-enz

Mycolic acid

Long Chain ACP-Enoyl Fatty Acid Reductase (inhA)

R

ACPO

APC: Acyl carrier protein)

N

O

NH2

H H

NADH co-enzymeinhA

1,4 hydride add.

R

ACPO

N

O

NH2

NAD+

CH3(CH2)1'7 14CO2H

17

OH ((CH2)23CH3

15CO2H

17

OH((CH2)23CH3

α-mycolαtes

O

CH3(CH2)17

ketom ycolαtes

15CO2H17

OH((CH2)23CH3

CH3(CH2)17

m ethoxym ycolαtes

H3CO

Page 24: Chemotherapeutic Agents / Antibiotics, chapter 34-39

First-line drugs

OH OH

OH

N

N

NH

O

OOHOH

HO

MeCO2

MeO

O

O

Rifampicin

Inhib. RNA-synth.

RifampicinRimactan®

Broad spectrum antibioticFrom Streptomyces spInhib bacterial RNA polymerase(- intract. naphtalene rings aromatic AA?)Induce CYP2C; increased metabol. of certain anti AIDS drugs

Pyrazinamide

N

O NHNH2

Isoniazide

NN

O NHNH2

Mechanism not known

Ethambutol

NH

HN

OH

HO

Mechanism not fully knownSynth of cell wall comp.:Inhib. arabinocyl transferase?Arabinose, Arabinomannan and Lipoarabinomannan

Page 25: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Second-line drugs

Ethionamide p-Aminosalicylic acid CycloserineIsolated Spreptomyces sp

N

O NHNH2

Isoniazide

N

S NH2

Mech. ≈ Isoniazide

CO2HOH

NH2

PABA antimetabolite

Folic acid synth (≈antibact. sulfa)

ONH

H2N O

Inhib. alanine racemaseand alanine ligase;Inhib. peptidoglycan synth

HO

O

O

NH2

NH2

O

R

NH2

O

OHH2N

HO

HO

HO

R=OH: Kanamycin AR=NH2: Kanamycin B

Kanamycin(aminoglycoside antibiotics)

Page 26: Chemotherapeutic Agents / Antibiotics, chapter 34-39

Others

Quinolones

N

OCO2H

R

FR

RR

O N N

O

O

F

NH

O

Oxazolidinones

Treatment of MAC infections

O

O

O

MeOO

O

NHO

HOHO

O

OO

OH

Clarithromycin(Macrolide)

Other macrolides

Ethambutol

Quinolones

Rifabutin (Rifamycin)