Kabataang Makabayan Handbook 1964 (First National Congress, 30 Nov 1964)
Therapeutics from the family of nucleoside and nucleotide ... · antileukemic agents 5-azacytidine...
Transcript of Therapeutics from the family of nucleoside and nucleotide ... · antileukemic agents 5-azacytidine...
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Therapeutics from the family of nucleoside and nucleotide analogs:
A contribution of the Czech science to world medicine
Marcela Krečmerová Institute of Organic Chemistry and Biochemistry ASCR, v.v.i.
Gilead Sciences & IOCB Research Centre
25th SVU Congress, June 27- July 3 2010, Tábor
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Institute of Organic Chemistry and Biochemistry ASCR, v.v.i. - established 1953
The greatest credit for estabilishing and developing the Institute belongs to Professor František Šorm (1913-1980).
Scientific interests: Natural compounds – terpenes, biologically active components of plants, antimetabolites of nucleic acid constituents as potential cancerostatics or antivirals.
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Scientific history
The sixties, 20th century• IOCB is one of 4 world institutions successful in oligonucleotide synthesis (J. Smrt, S. Chládek)
• Synthesis and studies of chemically modified nucleosides and their metabolites - F. Šorm, A. Pískala, J. Žemlička, J.Pitha, J. Veselý, A. Čihák, K.Raška: antileukemic agents 5-azacytidine (1964) 2´-deoxy-5-azacytidine (1964)
Approved by FDA for the treatment of acute myelodysplastic syndrom - 40 years later (!!!) 2004: 5-azacytidine, VidazaTM 2006: 2´-deoxy-5-azacytidine, DacogenTM
At present – Clinical investigation of 5-azacytidine in the treatment of solid tumors
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RNDr. Alois Pískala, CSc.
O
OH
HO
N
N
N
NH2
O
O
OH
HO
N
N
N
NH2
O
OH
azacitidineVidazaTM
2004
decitabine DacogenTM
2006
Produced by SuperGen, U.S.A.
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BIOCHEMICAL PROPERTIES OF 5-AZACYTIDINE – DISCOVERIES MADE IN IOCB:
• The compound has an antiproliferative activity • Phosphorylation in the cell to mono- di- and triphosphate• 5-Azacytidine triphosphate is an substrate for RNA polymerases.
• Incorporation of 5-azacytidine triphosphate to t-RNA, mRNA a preribosomal RNA
inhibition of synthesis of ribosomes and proteins
Pískala, Šorm, Veselý, Čihák, Zadražil, Fučík, Pačes (1964-1978)
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5-AZACYTIDINE WORKS ON EPIGENETIC PRINCIPLE AS AN INHIBITOR OF DNA METHYLATIONS.
Undesired methylations in DNA = the addition of Me group to a stretch of DNA which can lock or silence genes which are normally responsible for
the cell growth control. This process can be reversible.
Possibility of transformation of cancer cells to normal healthy cell by the action of inhibitors of DNA methylations. It is not necessary to kill the cancer cell, it can be repared.
5-AZACYTIDINE WORKS ON EPIGENETIC PRINCIPLE AS AN INHIBITOR OF DNA METHYLATIONS.
Undesired methylations in DNA = the addition of Me group to a stretch of DNA which can lock or silence genes which are normally responsible for
the cell growth control. This process can be reversible.
Possibility of transformation of cancer cells to normal healthy cell by the action of inhibitors of DNA methylations. It is not necessary to kill the cancer cell, it can be repared.
1980, Peter A. Jones USC School of Medicine, L.A., USA:
Synthesis of 5-azacytidine according to an original paper of Alois Pískala (Collection Czech Chem. Commun.1964, 29, 2060-2076) and investigation of its mechanism of action.
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Vidaza May Be Safe And Effective In MDS Patients Of All Ages (ASH 2009)By Gillian Losh Published: Jan 22, 2010 5:54 pm
Vidaza (azacytidine) may be as effective and well tolerated in myelodysplastic syndromes (MDS) patients aged 80 years and above as compared to patients less than 80 years old, according to a retrospective analysis by French researchers.The findings were presented at the 51st Annual Meeting of American Society of Hematology (ASH) meeting in December 2009.MDS patients aged 80 years and above make up 30 to 35 percent of all MDS patients. These patients are usually not candidates for chemotherapy, even at low doses, because older patients typically do not respond well to the side effects of chemotherapy. Instead, they generally only receive supportive care, which may help improve quality of life but does not treat MDS.
O
OH
HO
N
N
N
NH2
O
OH
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VIDAZA is the first and only agent proven to extend overall survival vs CCR in patients with higher-risk MDS
In the largest randomized study ever conducted in patients with higher-risk MDS, VIDAZA significantly extended overall survival vs conventional care regimens.
O
OH
HO
N
N
N
NH2
O
OH
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N
NNH
N
NH2
NH
NNH
N
O
NH2
N
NH
NH2
O
NH
NH
O
O
NH
NH
O
O
O
OHOH
HO
(H)
BasePossibilities of chemicalmodifications ofnucleosides:
sugar moiety
Base:
Adenine Thymine Guanine Cytosine Uracil
MOST OF RATIONALLY DEVELOPED ANTIVIRALS AND MANY CYTOSTATICS ARE MODIFIED NUCLEOSIDES
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Chemically modified nucleosides, nucleotides andnucleobases can work as antimetabolites in the process of nucleic acid metabolism.
ANTIMETABOLITE is a CHEMICALLY MODIFIED MOLECULE OF A NATURAL METABOLITE ABLETO INFLUENCE SOME ENZYME REACTIONS.
ANTIMETABOLITES CAN INFLUENCE PROCESSES IN CELLS (NEOPLASIA) AS WELL AS IN CELL PARASITES (VIRUSES, PARASITES, FUNGI).
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First generation antimetabolites
Maximum structural resemblance to natural metabolites
O
OH
HO
N
N
NH2
O
HO
Cytosine arabinoside
N
NNH
N
SH
6-Mercaptopurine
NH
NH
O
O
F
Fluorouracil
TREATMENT OF LEUKEMIA
TREATMENT OF LEUKEMIA
ANTITUMOR THERAPEUTICSANTITUMOR THERAPEUTICS
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2nd Generation of antimetabolites
Structural resemblance to natural metabolite is only in some basic aspects
ACYCLIC NUCLEOSIDE ANALOGS
The seventies of the 20th century
Carbohydrate moiety of the molecule is substituted with an aliphatic chain containing OH groups
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ANTIVIRALS made in IOCB
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HISTORY
The sixties of the 20th century – nucleoside analogs mostly developed as potencial cytostatics
Tepid interest of pharmaceutical companies to develop antivirals
Turning point – the beginning of the seventies:
A large „epidemy“ of genital herpes (HSV-2) in USA due to a promiscuous life style of then society
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Genital herpes caused by HSV-2
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N
HN N
N
O
H2N
OOH
N
HN N
N
O
H2N
OOH
OHN
HN N
N
O
H2N
OH
OH
N
N N
NH2N
OH
OH
ACYCLOVIR GANCICLOVIR PENCICLOVIR
N
HN N
N
O
H2N
OO
O
NH2
VALACYCLOVIR FAMCICLOVIR
ACYCLIC NUCLEOSIDE ANALOGS DERIVED FROM GUANINE
ANTIHERPETIC AGENTS
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Gertrude B. Elion (1918-1999) – development of acyclovir (ZOVIRAX)
The fifties 1988
1988 – Nobel Prize for medicine (together with Georg Hitchings) The first Nobel Prize targeted to pharmaceutical industry
N
HN N
N
O
H2N
OOH
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1970-1985, IOCB, Antonín Holý:Acyclic analogs of adenosine
N
N N
N
NH2
HO
N
N N
N
NH2
HO OH
HOOC
N
N N
N
NH2
HOOCOH
N
N N
N
NH2
ROOCOH
(S)-DHPA D-eritadenine AHPA a its esters
9-(2,3-Dihydroxypropyl)adenine 3-(Adenin-9-yl)-2-hydroxy- propanoic acid
OH
DHPA - antiherpetic drug Duviragel(Only S-enantiomer is antivirally active).
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ACYCLIC NUCLEOSIDE PHOSPHONATES (ANPs)
Biological activities:
ANTIVIRALS CYTOSTATICS ANTIPARAZITIC ACTIVITY (MALARIA, Trypanosoma brucei) IMMUNOMODULATORY ACTIVITY
Biological activities:
ANTIVIRALS CYTOSTATICS ANTIPARAZITIC ACTIVITY (MALARIA, Trypanosoma brucei) IMMUNOMODULATORY ACTIVITY
O P(O)(OH)2
R
R = H, OH, CH3, CH2F
BASE
1986 Antonin Holy reports ANPs as a new type of nucleotide antimetabolites
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STRUCTURAL TYPES OF ACYCLIC NUCLEOSIDE PHOSPHONATES
1. HPMP DERIVATIVES (S)-3-Hydroxy-2-(phosphonomethoxy)propyl derivatives
N
N
O
NH2
OHO P(O)(OH)2
OHO P(O)(OH)2
N
NN
N
NH2
(S)-HPMPC (S)-HPMPA
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N
N
O
NH2
OHO P(O)(OH)2
(S)-HPMPC: CIDOFOVIR, VISTIDETM
(Gilead Sciences)
• Synthesis: 1986 (A. Holý)• Approved by FDA: 1996 for the treatment of cytomegalovirus retinitis in AIDS patients • Intravenous application
Activity: all DNA viruses„Out of label“ used also for treatment of HSV infections (herpes genitalis), papilomavirus infections, progressive multifocal leukoencephalopathy, molluscum contagiosum, orf (and other poxvirus infections), adenovirus infections, Kaposi sarcoma
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2.PMP- DERIVATIVES (R)-2-(Phosphonomethoxy)propyl derivatives
N
N N
N
NH2
CH3
O P(O)(OH)2
N
N N
N
NH2
CH3
O
P OO
O
O
O
O
O
OO
PMPA – tenofovir Prodrug form: Bis-(POC)-PMPA: Tenofovir disoproxil
At present the best selling drug against AIDS.
The drug inhibits HIV multiplication. It cannot destroy the virusaltogether, but delays AIDS development in HIV-infected patients.
Newly approved for the treatment for Hepatitis B infections.
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Viread™ (tenofovir disoproxil)
approved 2001
Atripla™ (tenofovir disoproxil + emtricitabine + efavirenz)
approved 2006
Truvada™ (tenofovir disoproxil +emtricitabine) approved 2004
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Antiretroviral drugs – the present state: 28 Compounds and combinations available• Affecting diverse stages of virus development• Devided to several groups according to mechanism of action: Reverse transcriptase inhibitors Nucleoside: AZT, didanosine, zalcitabine,... Nucleotide: tenofovir (Viread), Non-nucleoside: efavirenz (Sustiva®)
HIV protease inhibitors (ritonavir, nelfinavir)
Fusion inhibitors block virus entry to the cell through the cell membrane Combined therapy – several compounds in 1 product (Atripla = efavirenz + tenofovir DF + emtricitabine) 1 tablet daily
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3. PME- DERIVATIVES 2-(Phosphonomethoxy)ethyl derivatives
O P(O)(OH)2
N
NN
N
NH2
O P(O)(OH)2
N
NN
N
NH2
NH2
O P(O)(OH)2
N
NN
N
NH
NH2
O P(O)(OH)2
NH
NH
N
N
O
NH2PMEA PMEG
PMEDAP cPrPMEDAP
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O P(O)(OH)2
N
NN
N
NH2
O
N
NN
N
NH2
PO
O
OO
O
OO
PMEA, 9-(2-Phosphonomethoxyethyl)adenine (adefovir)
Clinically used in a form of the prodrugAdefovir Dipivoxil (Bis-POM-PMEA)= bis(pivaloyloxymethyl) ester
HepseraTM
(Gilead Sciences)
Treatment of Hepatitis B
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GS-9219Compound developed in collaboration of IOCB (A.Holý) and Gilead Sciences
Clinical Phase I
O P(O)(OH)2
N
NN
N
NH
NH2
O P(O)(OH)2
NH
NH
N
N
O
NH2
GS-9219
O P
N
NN
N
NH
NH2O
HN
HNCOOEt
CH3H3C
COOEt
PMEG
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PMEG in cancer cell:• Phosphorylation
• Incorporation to the nucleic acid
• Completion of DNA replication
• Cancer cell death
GS-9219
Utilization of GS-9219: • non-Hodgkin lymphoma and chronic lymphatic leukemia
• High effectivity in vivo: 1 injection of GS-9219 caused a complete disappearance of tumors after 6 days (Beagle dogs)Present state: Clinical Phase I
Drug in the market: ??? 6-8 years
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N
N
NH2
O
OHO P(O)(OH)2
N
NN
N
NH2
O
O P(O)(OH)2
N
N
N
NH2
O
O P(O)(OH)2
N
N
NH2
O
OH
O P(O)(OH)2
N
N
N
NH2
O
O
N
P(O)(OH)2H
CH3
N
N
NH 2
O
OH
O
N
P(O)(OH)2
N
N
NH2
O
OHO
NH
P(O)(OH)2
low activity
low activitystrong activity against all DNA viruse
no activity inactive
low activity low activity
ACYCLIC NUCLEOSIDE PHOSPHONATES WITH A TRIAZINE BASE - antiviral activity
Krečmerová M., Holý A. et al. : J. Med. Chem. 2007, 50, 1069-1077.
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1-(S)-[3-Hydroxy-2-(phosphonomethoxypropyl]--5-azacytosine (HPMP-5azaC)
5-azacytosine analog of cidofovir
A selective activity against DNA viruses: adenovirus, poxviruses (vaccinia virus, cowpox virus, orf virus), herpesviruses (HSV-1, HSV-2, VZV, cytomegalovirus, HHV-6)
Comparison with cidofovir:• Similar activity (EC50): HSV-1, HSV-2, vaccinia• Higher activity (2-7 fold ): VZV, HCMV, Ad2, HHV-6• Lower toxicity (CC50)
2-12 fold higher selectivity index (i.e. ratio of CC50 to EC50 )
N
N N
O
NH2
OHO P(O)(OH)2
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N
N
N
O
OO P O
NH2
O(CH2)2 O-(CH2)15CH3
MK-612
The most active compound against cytomegalovirus:EC50 0.00026 nmol/mL(HCMV - Davis strain)• preclinical investigations finished • complicated metabolic profile
Lipophilic prodrug ofHPMP-5-azaC
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Discovery of a drug candidate, preclinical
tests
Phase I Phase II Phase III Approval Phase IV post-
marketing tests
6.5 years1.5
years2
years 3.5 years1.5
years
Clinical trials
Development of a new drug is Development of a new drug is a 15 years lasting process ...a 15 years lasting process ...
... and costs 800 million to 1 billion ... and costs 800 million to 1 billion $$
6000 active compounds 1 compound6-7 2-3
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Thank you for your attention !