Compound - Results

Allylestrenol

Java required.


Information Structure
Name Allylestrenol
Synonyms
17-(2-Propenyl)estr-4-en-17-ol
17-alpha-Allyl-17-beta-hydroxy-4-estrene
17-alpha-Allyl-17-beta-hydroxy-delta(sup 4)-estren
17-alpha-Allyl-3-deoxy-19-nortestosterone
17-alpha-Allyl-4-oestrene-17-beta-ol
17-alpha-Allylestr-4-en-17-beta-ol
17-alpha-Allylhydroxy-19-nor-4-androstene
17-Hydroxy-17-alpha-allyl-4-estrene
17alpha-Allyl-17beta-hydroxy-4-estrene
17alpha-Allyl-19-nor-delta-4-androstene-17beta-ol
17alpha-Allyl-3-deoxy-19-nortestosterone
17alpha-Allyl-4-destrene-17beta-ol
17alpha-Allyl-4-estren-17beta-ol
17alpha-Allyl-4-oestrene-17beta-ol
17alpha-Allylestrenol
19-Nor-17-alpha-preg-4-en-17-ol, 21-methylene-
21-Methylene-19-nor-17-alpha-preg-4-en-17-ol
3-Deoxy-17-alpha-allyl-19-nortestosterone
4-06-00-04143 (Beilstein Handbook Reference)
Alilestrenol
Allilestrenolo
Allylestrenol
Allylestrenolum
Allyloestrenol
Allyloestrenolum
BRN 3148038
EINECS 207-082-9
Estrenol, Allyl-
Gestanin
Gestanol
Gestanon
Gestanyn
NSC 37723
Orageston
Organon
Turinal
ATC G03DC01
CID 235905
CAS 000432600
Drugbank ID DB01431
SMILES C[C@@]12CC[C@@H]3[C@H](CCC4=CCCC[C@@H]34)[C@@H]1CC[C@@]2(O)CC=C
Formula C21H32O
Molweight 300.478
Atoms 26
LogP 5.2564
Rotatable Bonds 2
H-Bond Donors 0
H-Bond Acceptors 1
CYP interactions
NameRelationsReferences
3A4Substrate 11871398
Norethisterone

Java required.


Information Structure
Name Norethisterone
Synonyms
(17-alpha)-17-Hydroxy-19-norpregn-4-en-20-yn-3-one
17-alpha-19-Norpregn-4-en-20-yn-3-one, 17-hydroxy-
17-alpha-Ethinyl-17-beta-hydroxy-delta(sup:4)-estren-3-one
17-alpha-Ethinylestra-4-en-17-beta-ol-3-one
17-alpha-Ethynyl-17-beta-hydroxy-19-norandrost-4-en-3-one
17-alpha-Ethynyl-17-hydroxy-4-estren-3-one
17-alpha-Ethynyl-19-norandrost-4-en-17-beta-ol-3-one
17-alpha-Ethynyl-19-nortestosterone
17-alpha-Ethynyl-4-estren-17-ol-3-one
17-beta-Hydroxy-19-norpregn-4-en-20-yn-3-one
17-Ethinyl-19-nortestosterone
17-Hydroxy-19-nor-17-alpha-pregn-4-en-20-yn-3-one
17-Hydroxy-19-nor-17alpha-pregn-4-en-20-yn-3-one
17alpha-Ethinyl-17beta-hydroxy-delta(sup:4)-estren-3-one
17alpha-Ethinyl-19-nortestosterone
17alpha-Ethinylestra-4-en-17beta-ol-3-one
17alpha-Ethynyl-17-hydroxy-4-estren-3-one
17alpha-Ethynyl-17beta-hydroxy-19-norandrost-4-en-3-one
17alpha-Ethynyl-19-norandrost-4-en-17beta-ol-3-one
17alpha-Ethynyl-19-nortestosterone
17alpha-Ethynyl-4-estren-17-ol-3-one
17beta-Hydroxy-19-norpregn-4-en-20-yn-3-one
19-Nor-17-alpha-ethynyl-17-beta-hydroxy-4-androsten-3-one
19-Nor-17-alpha-ethynylandrosten-17-beta-ol-3-one
19-Nor-17-alpha-ethynyltestosterone
19-Nor-17-ethinyl Testosterone
19-Nor-17-ethinyltestosterone
19-Nor-17alpa-ethynyltestosterone
19-nor-17alpha-Ethynyl-17beta-hydroxy-4-androsten-3-one
19-nor-17alpha-Ethynylandrosten-17beta-ol-3-one
19-nor-17alpha-Ethynyltestosterone
19-Nor-17alpha-pregn-4-en-20-yn-3-one, 17-hydroxy-
19-Nor-ethindrone
19-Nor-ethinyl--4,5-testosterone
19-Norethinyltestosterone
19-Norethisterone
19-Norpregn-4-en-20-yn-3-one, 17-hydroxy-, (17alpha)-
19-Nortestosterone, 17-ethynyl-
4-08-00-01221 (Beilstein Handbook Reference)
AI3-26422
Anhydrohydroxynorprogesterone
Anovulatorio
Anovule
Brevinor 21
Brevinor 28
Brevinor-1 21
Brevinor-1 28
BRN 1915671
CCRIS 484
Ciclovulan
Conludaf
Conludag
EINECS 200-681-6
Estr-4-en-3-one, 17alpha-ethynyl-17-hydroxy-
Estrinor
Ethinyl-19-nortestosterone
Ethinylnortestosterone
Ethynylmortestosterone
Ethynylnortestosterone
Gencept
Genora
Gestest
HSDB 3370
Jenest-28
Microneth
Micronett
Micronor
Micronovum
Milli
Mini-pe
Mini-pill
Minovlar
N.E.E.
Nelova
Nodiol
Nor-Q.D.
Noraethisteronum
Noralutin
Norcept-E
Norcolut
Noresthisterone
Norethadrone
Norethin
Norethindrone
Norethisteron
Norethisterone
Norethisteronum
Norethyndron
Norethynodron
Norethynodrone
Noretisterona
Noretisterone
Norfor
Norgestin
Noriday
Noriday 28
Norluten
Norlutin
Norluton
Norpregneninlone
Norpregneninotone
NSC-9564
Orlest
Ortho 1 35
Ortho 7 7 7
Ortho-Novum 1 35
Ortho-Novum 1 50
Ortho-Novum 7 7 7
Ovysmen 0.5 35
Ovysmen 1 35
Primolut-N
Proluteasi
SC 4640
Synphase
Synphasic 28
Triella
Trinovum 21
Utovlan
Utovlar
ATC G03AC01
G03DC02
CID 4536
CAS 000068224
Drugbank ID DB00717
SMILES C[C@]12CC[C@H]3[C@@H](CCC4=CC(=O)CC[C@H]34)[C@@H]1CC[C@@]2(O)C#C
Formula C20H26O2
Molweight 298.419
Atoms 22
LogP 3.4925
Rotatable Bonds 0
H-Bond Donors 0
H-Bond Acceptors 2
CYP interactions
NameRelationsReferences
2C19Inducer medicine.iupui.edu/flockhart
3A4Substrate 14663455
3A5Substrate 14663455
3A7Substrate 14663455
Lynestrenol

Java required.


Information Structure
Name Lynestrenol
Synonyms
(17-alpha)-19-Norpregn-4-en-20-yn-17-ol
17-alpha-Ethinyl-17-beta-hydroxyestr-4-ene
17-alpha-Ethinyl-17-beta-hydroxyoestr-4-ene
17-alpha-Ethynil-delta-4-estrene-17-beta-ol
17-alpha-Ethynylestr-4-en-17-beta-ol
17-alpha-Ethynylestrenol
17-alpha-Ethynyloestr-4-en-17-beta-ol
17-alpha-Ethynyloestrenol
17alpha-Ethynylestrenol
19-Nor-17alpha-pregn-4-en-20-yn-17-ol
3-Desoxynorlutin
delta(sup 4)-17-alpha-Ethinylestren-17-beta-ol
delta(sup 4)-17-alpha-Ethinyloestren-17-beta-ol
delta4-17alpha-Ethinylestren-17beta-ol
EINECS 200-151-4
Endometril
Estr-4-en-17beta-ol, 17-ethynyl-
Ethinyl Oestrenol
Ethinylestrenol
Ethinyloestranol
Ethynloestrenol
Ethynylestrenol
Exluten
Exlution
Exluton
Exlutona
IND 1006
Linestrenol
Linestrenolo
Lynenol
Lynestrenol
Lynestrenolum
Lynoestrenol
Lynstranol
NSC-37725
ORG 485-50
Orgametil
Orgametril
Orgametrol
ATC G03AC02
G03DC03
CID 5857
CAS 000052766
SMILES C[C@]12CC[C@H]3[C@@H](CCC4=CCCC[C@H]34)[C@@H]1CC[C@@]2(O)C#C
Formula C20H28O
Molweight 284.436
Atoms 25
LogP 4.3135
Rotatable Bonds 0
H-Bond Donors 0
H-Bond Acceptors 1
CYP interactions
NameRelationsReferences
2C9Inducer 18356043
2C19Substrate Inducer 18356043
3A4Substrate 18356043
Ethisterone

Java required.


Information Structure
Name Ethisterone
Synonyms
17-alpha-Ethynyltestosterone
17-beta-Hydroxy-17-alpha-ethynyl-4-androsten-3-one
17-Ethinyl Testosterone
17-Ethinyltestosterone
17-Hydroxy-17-alpha-pregn-4-en-20-yn-3-one
17alpha-Ethinyl Testosterone
17alpha-Ethinyltestosterone
17alpha-Ethynyltestosterone
4-08-00-01225 (Beilstein Handbook Reference)
Aethisteron
Aethisteronum
AI3-26421
Androst-4-en-3-one, 17alpha-ethynyl-17-hydroxy-
Anhydrohydroxyprogesterone
Anhydroxyprogesterone
BRN 1889895
Colutoid
EINECS 207-096-5
Ethinone
Ethinyl Testosterone
Ethinyltestosterone
Ethisterone
Ethisterone Anhydrohydroxyprogesterone
Ethisteronum
Ethynyltestosterone
Etisterona
Etisterone
Gestoral
Lucorteum Oral
Lutidon Oral
Lutocylol
Nalutoral
NSC 9565
Nugestoral
Ora-Lutin
Praegninum
Pranone
Pregneninolone
Pregnin
Primolut C
Prodoxan
Prodroxan
Produxan
Progestab
Progestin P
Progestolets
Progestoral
Prolutol
Proluton C
Prone
Syngestrotabs
Testosterone, 17-ethynyl-
Trosinone
ATC G03DC04
CID 2754191
CAS 000434037
SMILES C[C@@]12CCC(=O)C=C1CC[C@H]3[C@H]2CC[C@]4(C)[C@H]3CC[C@@]4(O)C#C
Formula C21H28O2
Molweight 312.446
Atoms 26
LogP 3.8826
Rotatable Bonds 0
H-Bond Donors 0
H-Bond Acceptors 2
Tibolone

Java required.


Information Structure
Name Tibolone
Synonyms
(17r)-17-hydroxy-7alpha-methyl-19-norpregn-5(10)-en-20-yn-3-one
(7alpha,17alpha)-17-hydroxy-7-methyl-19-norpregn-5(10)-en-20-yn-3-one
(7alpha,17beta)-17-ethynyl-17-hydroxy-7-methylestr-5(10)en-3-one
(7beta,8xi,9beta,13alpha,14beta,17alpha)-17-ethynyl-17-hydroxy-7-methylestr-5(10)-en-3-one
(7r,8r,9s,13s,14s,17r)-17-ethynyl-17-hydroxy-7,13-dimethyl-1,2,4,6,7,8,9,11,12,14,15,16-dodecahydrocyclopenta[a]phenanthren-3-one
17-Hydroxy-7alpha-methyl-19-nor-17alpha-pregn-5(10)-en-20-yn-3-one
17alpha-ethynyl-17beta-hydroxy-7alpha-methylestr-5(10)-en-3-one
5630-53-5
ac-20036
ac1l9fjg
ambap5630-53-5
boltin
chebi:32223
cid444008
cpd000469219
d01639
EINECS 227-069-1
hms2052k21
hms2090b10
kb-889
livial
liviella
mls001424234
org-od14
sam001246801
smr000469219
Tibolona
Tibolone
tibolone (jan/usan/inn)
Tibolonum
tl8003648
xyvion
zinc03812889
ATC G03DC05
G03CX01
CID 444008
CAS 005630535
SMILES C[C@@H]1CC2=C(CCC(=O)C2)[C@H]3CC[C@@]4(C)[C@@H](CC[C@@]4(O)C#C)[C@H]13
Formula C21H28O2
Molweight 312.446
Atoms 27
LogP 3.8826
Rotatable Bonds 0
H-Bond Donors 0
H-Bond Acceptors 2
CYP interactions
NameRelationsReferences
1A2Inhibitor 11792677
2C9Inhibitor 11792677
2E1Inhibitor 11792677
3A4Inhibitor 11792677
19AInhibitor 17467267
Phase2 interactions
NameReferences
SUL 16360722,
15145448,
16879988,
16857224
Etynodiol

Java required.


Information Structure
Name Etynodiol
Synonyms
(3-beta,17-alpha)-19-Norpregn-4-en-20-yne-3,17-diol
17-alpha-Ethynyl-19-norandrost-4-ene-3-beta,17-beta-diol
Aethynodiolum
EINECS 214-971-5
Ethinodiol
Ethynodiol
Etinodiol
Etinodiolo
Etynodiol
Etynodiolum
ATC G03DC06
CID 9270
CAS 001231932
Drugbank ID DB00823
TTD Drug ID DAP000856
SMILES C[C@]12CC[C@H]3[C@@H](CCC4=C[C@@H](O)CC[C@H]34)[C@@H]1CC[C@@]2(O)C#C
Formula C24H32O4
Molweight 384.508
Atoms 28
LogP 4.4259
Rotatable Bonds 4
H-Bond Donors 0
H-Bond Acceptors 4
Methylestrenolone

Java required.


Information Structure
Name Methylestrenolone
Synonyms
17-alpha-Methyl-17-beta-hydroxy-4-estren-3-one
17-beta-Hydroxy-17-methylestr-4-en-3-one
17-Methyl-19-nortestosterone
17alpha-Methyl-17beta-hydroxy-19-nor-4-androsten-3-one
17alpha-Methyl-19-nortestosterone
17alpha-Methylestrenolone
19-Nor-17-alpha-methyltestosterone
19-Nortestosterone, 17-methyl-
4-08-00-01001 (Beilstein Handbook Reference)
AI3-52808
BRN 2622263
EINECS 208-183-0
Lutenin
Matronal
Metalutin
Methalutin
Methylestrenolone
Methylnortestosterone
Methyloestrenolone
Normetandrone
Normethandrolone
Normethandrone
Normethanedrolone
NSC 10039
Orgasteron
ATC G03DC31
CID 5284597
CAS 000514614
SMILES C[C@]1(O)CC[C@H]2[C@H]3CCC4=CC(=O)CC[C@H]4[C@@H]3CC[C@@]12C
Formula C19H28O2
Molweight 288.424
Atoms 25
LogP 3.8792
Rotatable Bonds 0
H-Bond Donors 0
H-Bond Acceptors 2