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MEDICINAL CHEMISTRY CHEM-E4220 chapter #5: steroid hormones Jan Deska Bioorganic Chemistry www.deskalab.com 16.11.2021

CHEM-E4220 MEDICINAL CHEMISTRY

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Page 1: CHEM-E4220 MEDICINAL CHEMISTRY

MEDICINAL CHEMISTRYCHEM-E4220

chapter #5: steroid hormones

Jan DeskaBioorganicChemistry

www.deskalab.com

16.11.2021

Page 2: CHEM-E4220 MEDICINAL CHEMISTRY

TODAY'S MENU

ü second lecture on steroid molecules

ü hormonal regulation influenceseverything from urine production tocancer growth

ü key ingredients in birth control

Jan DeskaBioorganicChemistry

Page 3: CHEM-E4220 MEDICINAL CHEMISTRY

INTENDED LEARNING OUTCOMES

ü to have a basic understanding of the functionof nuclear receptors

ü to distinguish the four basic steroid hormonefamilies

ü to explain the principle of contraceptive pills

Jan DeskaBioorganicChemistry

Page 4: CHEM-E4220 MEDICINAL CHEMISTRY

Hormone-control: Regulatory processes

Page 5: CHEM-E4220 MEDICINAL CHEMISTRY

Nuclear receptors

§ ligand-activated transcription factors

§ activate transcription of specificgenes

§ control the cellular production ofproteins and hence up- ordownregulate certain functions

Page 6: CHEM-E4220 MEDICINAL CHEMISTRY

Nuclear receptors

§ ligand-activated transcription factors

§ activate transcription of specificgenes

§ control the cellular production ofproteins and hence up- ordownregulate certain functions

§ consist of three domain:

ü coactivator recognition

ü DNA binding (shown right)

ü ligand binding

§ the human genom encodes for 48 nuclear receptors

Page 7: CHEM-E4220 MEDICINAL CHEMISTRY

nuclear receptor

hormone

coactivator RNA polymerase mRNA proteins

§ cytosolic nuclear receptors enter nucleusafter ligand binding (type 1)

Jan DeskaBioorganicChemistry

Nuclear Receptors

Page 8: CHEM-E4220 MEDICINAL CHEMISTRY

nuclear receptor

hormone

coactivator RNA polymerase mRNA proteins

§ cytosolic nuclear receptors enter nucleusafter ligand binding (type 1)

§ type 2, 3 and 4 nuclear receptors locatedinside the nucleus

Jan DeskaBioorganicChemistry

Nuclear Receptors

Page 9: CHEM-E4220 MEDICINAL CHEMISTRY

nuclear receptor

hormone

coactivator RNA polymerase mRNA proteins

§ cytosolic nuclear receptors enter nucleusafter ligand binding (type 1)

§ type 2, 3 and 4 nuclear receptors locatedinside the nucleus

§ agonistic binding triggers cascade:

• coactivator binding

• RNA polymerase association

• DNA reading and mRNA production

• mRNA translates to thecorresponding protein (via theribosome)

Jan DeskaBioorganicChemistry

Nuclear Receptors

Page 10: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

From Cholesterol to Steroid Hormones

adrenal glands: corticosteroids

testes: androgens

ovaries: estrogens

cholesterol

HO

H

H

cortisol

O OH

O OH

low-density

lipoprotein

Page 11: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

From Cholesterol to Steroid Hormones

adrenal glands: corticosteroids

H

R

OH

H

R = OH: testosterone COCH3: progesterone

testes: androgens

cholesterol

low-density

lipoprotein

HO

H

H

cortisol

O OH

O OH

Page 12: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

From Cholesterol to Steroid Hormones

adrenal glands: corticosteroids

H

OH

HOH

H

estradiol

H

R

OH

H

R = OH: testosterone COCH3: progesterone

testes: androgens

ovaries: estrogens

cholesterol

low-density

lipoprotein

HO

H

H

cortisol

O OH

O OH

Page 13: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Confused about all those Structures?

Counting carbons tells youwhat you're dealing with...

Page 14: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Confused about all those Structures?

HO

H

H

HO

H

H

cortisone

O OH

O OH

HO

H

HHO

O O OH

aldosterone

H

H

HOH

H

cholesterol

O

27 carbons

HO

H

H

O

progesterone17α-hydroxyprogesterone

OH

biosyntheticsidechaincleavage

biosyntheticsidechainoxygenation

H

OH

OH

H

H

O

OH

H

H

OH

HOH

H

estriol

H

OH

HOH

H

estradiol testosterone androdienone

biosyntheticretro-benzoin

OH

biosyntheticaromatisation

Counting carbons tells youwhat you're dealing with...

progestagens: 21 carbonsadrenal corticoids: 21 carbons + terminal OH

androgens: 19 carbonsestrogens: 18 carbons (and aromatic)

Page 15: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Transport of Steroid Hormones

unlike cholesterol, lipophilic steroidhormones are not transported fromthe glands to the target organs via lipoprotein vesicles

unspecific transport via albumins

+

task-specific globulines:

§ transcortin (corticosteroids)

§ sex hormone-binding globulin(antrogens and estrogens)

testosterone bound to albumin

Page 16: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Adrenal Hormones

Page 17: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Adrenal Hormones

Adrenal glands produce two types of steroid hormones

HO

H

HHO

O O OH

aldosteroneH

OH

H

O OH

deoxycorticosterone

§ mineralocorticoids

mainly responsible for water and electrolyte balance

Page 18: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Adrenal Hormones

Adrenal glands produce two types of steroid hormones

HO

H

HHO

O O OH

aldosteroneH

OH

H

O OH

deoxycorticosterone

synthetic mineralocorticoids used asdiuretics (= urine-producing effect), avoiding critical potassium loss

HO

H

H

spironolactone

O

O

SAc

§ mineralocorticoids

mainly responsible for water and electrolyte balance

Page 19: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Adrenal Hormones

Adrenal glands produce two types of steroid hormones

§ glucocorticoids

• regulate mechanisms of the immune system (upregulation of anti-inflammatoryproteins and down-regulation of pro-inflammatory proteins)

• metabolic functions such as gluconeogenesis and glucose uptake inhibition

• cognition function (memory and attention deficit disorders)

HO

H

H

cortisone

O OH

O OH

HO

H

HHO R

O OH

R = H: corticosteron OH: cortisol (= hydrocortisone)

Page 20: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Adrenal Hormones

Adrenal glands produce two types of steroid hormones

§ glucocorticoids

HO

H

H

cortisone

O OH

O OH

HO

H

HHO R

O OH

R = H: corticosterone OH: cortisol

cortisone (and adrenaline) as majorstress hormones

• elevates blood pressure and prepares for fight or flight response

• broad application as drug against allergies and inflammations, in autoimmune disorders and as immunosuppressant

Page 21: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Adrenal Hormones

Adrenal glands produce two types of steroid hormones

§ glucocorticoids

HO

H

H

cortisone

O OH

O OH

HO

H

HHO R

O OH

R = H: corticosterone OH: cortisol

cortisone (and adrenaline) as majorstress hormones

• elevates blood pressure and prepares for fight or flight response

• broad application as drug against allergies and inflammations, in autoimmune disorders and as immunosuppressant

• topical application in treatment of eczema and dermatitis

• inhalative treatment of bronchial asthma and sarcoidosis (inflammatorylumps in lung)

• direct injection into joints and ligaments (in case of inflammation, injury, rheumatoid arthritis,...)

Page 22: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Adrenal Hormones

Adrenal glands produce two types of steroid hormones

§ glucocorticoids

• but also: cortisone and hydrocortisone with impact on water and salt balance(glucocorticoid potency vs mineralocorticoid potency of cortisol = 1:1)

HO

H

HHO OH

O OH

cortisol

Page 23: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Adrenal Hormones

Adrenal glands produce two types of steroid hormones

§ glucocorticoids

• but also: cortisone and hydrocortisone with impact on water and salt balance(glucocorticoid potency vs mineralocorticoid potency of cortisol = 1:1)

synthetic analogues with reduced mineralocorticoid effects

HO

H

HHO

O OH

prednisoloneH

OCl

H

O OH

beclometasone

OHR

HO OH

HO

F

HHO

O OH

OH

dexamethasone

HO

H

HHO OH

O OH

cortisol

Page 24: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Adrenal Hormones

Adrenal glands produce two types of steroid hormones

§ glucocorticoids

• but also: cortisone and hydrocortisone with impact on water and salt balance(glucocorticoid potency vs mineralocorticoid potency of cortisol = 1:1)

synthetic analogues with reduced mineralocorticoid effects

mineralocorticoid potency:

anti-inflammatory potency:

cortisone cortisol prednisolone dexmethasone

0.8

0.8

1

1

0.6

4

<0.1

25

HO

H

HHO

O OH

prednisoloneH

OCl

H

O OH

beclometasone

OHR

HO OH

HO

F

HHO

O OH

OH

dexamethasone

HO

H

HHO OH

O OH

cortisol

Page 25: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Adrenal Hormones

Adrenal glands produce two types of steroid hormones

§ glucocorticoids

• but also: cortisone and hydrocortisone with impact on water and salt balance(glucocorticoid potency vs mineralocorticoid potency of cortisol = 1:1)

synthetic analogues with reduced mineralocorticoid effects

HO

H

HHO

O OH

prednisoloneH

OCl

H

O OH

beclometasone

OHR

HO OH

HO

F

HHO

O OH

OH

dexamethasone

HO

H

HHO OH

O OH

cortisol

despite no cross-talk with androgen receptors, use of glucocorticoids isbanned as doping by WADA (except some topical applications)

Page 26: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Glucocorticoids & COVID-19

Coronavirus disease 2019 (COVID-19)

§ caused by severe acute respiratory syndrome coronavirus 2

§ contagious viral infection that invades cells through binding of the viral spike proteins to the angiotensin-converting enzyme 2 (ACE2)

§ ACE2 is covering cell membranes, particularly:

• lung alveolar cells (type II)

• enterocytes of the small intestines

• endothelial cells of the blood vessels

• arterial smooth muscle cells

inflammation of upper (sinuses, throat) & lower respiratory tract (lungs)

impairment of gastrointestinal organs & kidneys

chronic damage of cardiovascular system

Page 27: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Glucocorticoids & COVID-19

P. Horby et al. New Engl. J. Med. 2020, DOI: 10.1056/NEJMoa2021436

§ dexamethasone established as treatment for severe cases of COVID-19

§ reduces inflammation, supports immune system

§ no direct anti-viral effect

§ benefitial only for hospitalized patients on oxygen therapy or on a ventilator

Page 28: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Glucocorticoids & COVID-19

P. Horby et al. New Engl. J. Med. 2020, DOI: 10.1056/NEJMoa2021436

§ dexamethasone established as treatment for severe cases of COVID-19

§ reduces inflammation, supports immune system

§ no direct anti-viral effect

§ benefitial only for hospitalized patients on oxygen therapy or on a ventilator

26%23%

discharged from hospital after 28 days:63.5% vs 67.2%

Page 29: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Glucocorticoids & COVID-19

https://www.covid19treatmentguidelines.nih.gov/management/clinical-management/hospitalized-adults--therapeutic-management/

accessed: 15.11.2021

Page 30: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Sex Hormones (gonadal steroids)

Page 31: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Sex Hormones

All sex hormones are found both in women and men, however, hormone levels anddistribution and concentration of receptors in particular tissues differ

§ responsible for development of secondary sex characteristics during puberty

§ produced by gonadal glands (ovaries and testes)

§ fertility and reproduction

§ various other regulating functions

Page 32: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Sex Hormones

All sex hormones are found both in women and men, however, hormone levels anddistribution and concentration of receptors in particular tissues differ

§ responsible for development of secondary sex characteristics during puberty

§ produced by gonadal glands (ovaries and testes)

§ fertility and reproduction

§ various other regulating functions

"male sex hormones": androgens

"female sex hormones": estrogens and progestogens

non-steroidal hormones: follicle-stimulating hormone, gonadotropin-releasinghormone,... (= glycoprotein hormones)

Page 33: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Sturctural Comparison between the Sex Hormones

H

OH

HOH

H

estradiolH

OH

OH

H

testosterone

nuclear receptors show very high affinities (down to 50 pM) with no crosstalk

flat phenol region

H-bond donor

additional methyl and half boat conformation

H-bond acceptor

Page 34: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Sturctural Comparison between the Sex Hormones

estradiol binding to its receptor

His524Arg394

Glu353

H2O

Leu387

Leu384

Page 35: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Sturctural Comparison between the Sex Hormones

testosterone binding to its receptor

Arg766

Gln725

Met759

Met756

Page 36: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Sturctural Comparison between the Sex Hormones

testosterone binding to its receptor

Arg766

Gln725

Met759

Met756

Page 37: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Female-"specific" Hormone Pharmaceuticals

Page 38: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Estrogen and progesterone receptors as target

DNA-bindingdomain

DNA hinge region ligandligand-binding domain

Page 39: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Estrogen and progesterone receptors as target

both estrogenic and anti-estrogenic effects can be exploited

estradiol binds agonistic

blue helix fillsout the groove

coactivator canassociate to thedimericactivatedreceptor

H

OH

HOH

H

estradiol

Page 40: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Estrogen and progesterone receptors as target

both estrogenic and anti-estrogenic effects can be exploited

tamoxifens bindsantagonistic

blue helix isrepelled by toobulky binder

coactivator incapableto coordinate andbind RNA polymerase

HO

O

4-hydroxytamoxifen

N

Page 41: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Hormone Contraceptives

Menstrual Cycle

ovulationmenses

1 2 3 4 285 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27

days of menstrual cycle

hormonelevels

ovariancycle

uterinecycle

egg developing follicle corpus luteum

§ combination ofestrogen andprogestogen modulateovarian cycle

§ estrogen supportsripening of egg andformation of follicles

§ progestogen supportsthe structure of theuterine lining(endometrium) andformation of thecervical mucus

estrogenprogestogen

FSHLH

ovary

uterus

cervix

H

OH

HOH

H

estradiolH

OH

H

progesterone

O

H

OH

HOH

H

estradiolH

OH

H

progesterone

O

Page 42: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Hormone Contraceptives

Menstrual Cycle

ovulationmenses

1 2 3 4 285 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27

days of menstrual cycle

hormonelevels

ovariancycle

uterinecycle

egg developing follicle corpus luteum

indirect effects

§ estrogen andprogestogen givenegative feedback tohypothalamus, modulating secretion ofgonadotropin-releasinghormone

§ GnRH lack decreasessecretion of follicle-secreting hormone(FSH) and luteinizinghormone (LH)

estrogenprogestogen

FSHLH

H

OH

HOH

H

estradiolH

OH

H

progesterone

O

ovary

uterus

cervix

H

OH

HOH

H

estradiolH

OH

H

progesterone

O

Page 43: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Hormone Contraceptives

The "father of the pill"

Carl Djerassi (1923 – 2015)

§ chemist, novelist, playwriter

§ early steroid studies, e.g. conversion oftestosterone to estrone (aromatase-like reaction)

§ development of first oral contraceptive based on norethisterone (1956)

H

OH

OH

HH3C oxidation

– CO2H

OH

HOH

H

H

OH

OH

H

Page 44: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Hormone Contraceptives

menses

1 2 3 4 285 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24 25 26 27

days of menstrual cycle

hormonelevels

ovariancycle

uterinecycle

egg ... no follicle formation and ripening

Birth Control Pills

§ prevents ovulation

§ progestogen(gestagene) inhibitsimplantation of egg into uterine wall

§ additional effect ofprogestogens: thickening ofcervical mucus toprevent spermentering the uterus

§ combined administration of estrogen & progestogene or progestogen-only pills

Page 45: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Hormone Contraceptives

Birth control pill

modern combined oral contraceptives based on synthetic analogues

estrogens progestins (= artificial progestogens)

H

O

HOH

H

estradiol cypionate

O

HHO

H

H

ethynylestradiol

OH

H

OH

OH

H

norethisterone

HO

H

H

drospirenone

O

O

Page 46: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Hormone Contraceptives

Oral contraceptive pill vs. IUS (intruterine system)

hormone IUS copper IUS

Page 47: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Hormone Contraceptives

Emergency contraceptives ("morning-after-pills")

H

OH

OH

H

levonorgestrel

H

progestin-type drugs

§ inhibit implantation of egg in endometrium(uterine lining)

Page 48: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Hormone Contraceptives

Emergency contraceptives ("morning-after-pills")

H

OH

OH

H

levonorgestrel

H

progestin-type drugs

§ inhibit implantation of egg in endometrium(uterine lining)

Page 49: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Hormone Contraceptives

Emergency contraceptives ("morning-after-pills")

H

OH

OH

H

levonorgestrel

H

HO

H

ulipristal acetate

O

O

O

N

progestin-type drugs

§ inhibit implantation of egg in endometrium(uterine lining)

antiprogestin-type drugs

§ progestogene receptor antagonists

§ (ulipristal acetate or mifepristone)

§ induce detachement of endometrium

Page 50: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Anti-progestins in Medical Abortion

Combination of anti-progestin and synthetic prostaglandins

mifepristoneH

OH

O

H

N

+

HO

OOMe

O

OH

misoprostol

HO

OOMe

O

gemeprostHO

§ weakening of uterine lining

§ myometrial contraction (uterine smooth muscle) to expulse tissue

Page 51: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Hormone Replacement Therapy

Treatment of menopause-related lack of estrogens by medication withestrogen receptor agonists

§ estrogen has multiple targets apart fromdirect reproductive organs

§ HRT reduces risk of coronary heartdiseases

§ HRT prevents bone loss andosteoporotic fractures

§ but: estradiol and first-generation estrogen mimics increase risk of breastcancer and endometrial tumors

H

OH

HOH

H

estradiol

diethylstilberolHO

OH

Page 52: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Hormone Replacement Therapy

Selective estrogen receptor modulators (SERMs)

§ SERMs act as selective agonist in bonebut exhibit (partial) antagonistic activityin breast and/or uterus endometrialtissue

§ resistances found in stilbene-type anti-estrogens due to upregulation ofestrogen receptor phosphorylation

§ third-generation: fulvestrant

O

tamoxifen

N

S

O

OH

Oraloxifen

N

H

OH

HOH

H

SO O F F

F

FF

5

fulvestrant

Page 53: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Aromatase Inhibitors

§ in pre-menopause, estrogen production occurs mainly in ovaries

§ post-menopause estrogen arises from aromatization of androgens in peripheraltissue, with little transport across the body

§ breast and ovarian cancer requires estradiol to grow

Page 54: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Aromatase Inhibitors

§ in pre-menopause, estrogen production occurs mainly in ovaries

§ post-menopause estrogen arises from aromatization of androgens in peripheraltissue, with little transport across the body

§ breast and ovarian cancer requires estradiol to grow

§ aromatase inhibitors (AI's) limit supply of estrogens of the fast-growing tissues

H

O

OH

H

exemestane

(steroidal AI's)

OH

H

testolactone

O OCNCN

NNN

N

CN

CN

NN

anastrozole

(non-steroidal AI's)

letrozole

Page 55: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Aromatase Inhibitors

§ in pre-menopause, estrogen production occurs mainly in ovaries

§ post-menopause estrogen arises from aromatization of androgens in peripheraltissue, with little transport across the body

§ breast and ovarian cancer requires estradiol to grow

§ aromatase inhibitors (AI's) limit supply of estrogens of the fast-growing tissues

§ in addition: used in treatment of male gynecomastia (benign growth of breast)

H

O

OH

H

exemestane

(steroidal AI's)

OH

H

testolactone

O OCNCN

NNN

N

CN

CN

NN

anastrozole

(non-steroidal AI's)

letrozole

Page 56: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Aromatase Inhibitors

§ in pre-menopause, estrogen production occurs mainly in ovaries

§ post-menopause estrogen arises from aromatization of androgens in peripheraltissue, with little transport across the body

§ breast and ovarian cancer requires estradiol to grow

§ aromatase inhibitors (AI's) limit supply of estrogens of the fast-growing tissues

§ in addition: used in treatment of male gynecomastia (benign growth of breast)

H

O

OH

H

exemestane

(steroidal AI's)

OH

H

testolactone

O OCNCN

NNN

N

CN

CN

NN

anastrozole

(non-steroidal AI's)

letrozole

Page 57: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Male-"specific" Hormone Pharmaceuticals

Page 58: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Progesterone receptor in male contraception

Combination of progestogen and androgen can significantly suppress spermatogensis

§ native role of progesterone in malesunknown (other than source of testosterone

§ however, progestogen receptors found in male hypothalamus

§ negative feedback suppression ofgonadotropins reduces also follicle-stimulating hormone

§ low FSH levels suppress spermatogenesisproteins in Sertoli cells in the testes

Wang et al., J. Clin. Endocrinol. Metab. 2008, 93, 1774-1783.Page, Amory, Bremner, Endocrin. Rev. 2008, 29, 465-493.

HO

H

H

medroxyprogesterone acetate

O

O

O

H

OH

OH

HH

etonogestrel

Page 59: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Androgen receptors as Pharma Targets

Agonistic binding of androgenic hormones (testosterone & dihydrotestosterone)

§ development of male sexual characteristics and regulation ofspermatogenesis

§ androgens support gain and maintenance of bone structure and skeletalmuscles

§ influence hair growth but likewise associated to pattern hair loss

H

OH

OH

H

testosteroneH

OH

OH

H

dihydrotestosteroneH

Page 60: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Androgen receptors as Pharma Targets

Agonistic binding of androgenic hormones (testosterone & dihydrotestosterone)

§ development of male sexual characteristics and regulation ofspermatogenesis

§ androgens support gain and maintenance of bone structure and skeletalmuscles

§ influence hair growth but likewise associated to pattern hair loss

§ also: essential factor in normal female fertility (regulates ovulation)

H

OH

OH

H

testosteroneH

OH

OH

H

dihydrotestosteroneH

Page 61: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Androgen receptors as Pharma Targets

Anabolic steroids as muscle and bone growth agent

§ synthetic androgens in the treatment ofgrowth failure diseases

§ bone marrow stimulation H

OH

OH

H

nandrolone

H

H

OH

OH

H

dianabol

H

OH

OH

H

drostanoloneH

Page 62: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Androgen receptors as Pharma Targets

Anabolic steroids as muscle and bone growth agent

§ synthetic androgens in the treatment ofgrowth failure diseases

§ bone marrow stimulation

but also

§ performance enhancing drugs

• often illegal and not properly controlled

• neuropsychiatic effects (mood disorders, aggression, dependence)

• development of female sexual characteristics (conversion to estrogensby aromatase)

• liver and kidney failure

H

OH

OH

H

nandrolone

H

H

OH

OH

H

dianabol

H

OH

OH

H

drostanoloneH

Page 63: CHEM-E4220 MEDICINAL CHEMISTRY

Jan DeskaBioorganicChemistry

Androgen receptors as Pharma Targets

Androgen receptor antagonists

§ anti-androgens in treatment of prostate cancer

• side effects: reduced sexual activity (chemical castration)

HO

H

H

cyproterone acetateCl

O

O

O

NH

HO

H

H

finasterideH

ONH

§ anti-androgens in treatment of breast cancer

• over-expression of androgen receptors in malign breast tissue

• similar to SERMs, also female androgenic receptors can beaddressed to decrease tumor risk

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SUMMARY

§ steroid hormone therapies as part of themost transformative developments formodern society

§ high specificity allows for nuclear receptorsto distinguish strikingly similar steroids withhigh fidelity

§ but: steroid metabolism can also changestructures and switch specificity from onereceptor to another

Jan DeskaBioorganicChemistry