Compound - Results

Hydrogen Peroxide

Java required.


Information Structure
Name Hydrogen peroxide
Synonyms
52%)
Albone
Albone 35
Albone 35CG
Albone 50
Albone 50CG
Albone 70
Albone 70CG
Albone DS
Caswell No. 486AAA
CCRIS 1060
Dihydrogen Dioxide
EINECS 231-765-0
Elawox
EPA Pesticide Chemical Code 000595
Hioxyl
HSDB 547
Hydrogen Dioxide
Hydrogen Dioxide Solution
Hydrogen Peroxide
Hydrogen Peroxide (H2O2)
Hydrogen Peroxide Solution (DOT)
Hydrogen Peroxide, 90%
Hydrogen Peroxide, Solution
Hydrogen Peroxide, Solution, 3%
Hydrogen Peroxide, Solution, 30%
Hydrogen Peroxide, Solution, 35%
Hydroperoxide
Inhibine
Interox
Kastone
Lensept
NSC 19892
Oxydol
Perhydrol
Perone
Perone 30
Perone 35
Perone 50
Perossido Di Idrogeno
Peroxaan
Peroxan
Peroxide
Peroxyde Dhydrogene
Superoxol
T-Stuff
UN 2014 (20%-52%)
UN 2984 (8%-20%)
Wasserstoffperoxid
Waterstofperoxyde
ATC A01AB02
D08AX01
S02AA06
CID 784
CAS 007722841
SMILES OO
Formula H2O2
Molweight 34.0147
Atoms 2
LogP 0.0174
Rotatable Bonds 0
H-Bond Donors 0
H-Bond Acceptors 2
CYP interactions
NameRelationsReferences
1B1Substrate 11074351
2D6Substrate 16987939
Phase2 interactions
NameReferences
GST 12063243,
20631055
Transporter
AC-No.NameReferences
P19634Sodium/hydrogen exchanger 1 16179939
Q86UG4Cancer/testis antigen 48 9439681
Chlorhexidine

Java required.


Information Structure
Name Chlorhexidine
Synonyms
1,1-Hexamethylenebis(5-(p-chlorophenyl)biguanide)
1,6-Bis(5-(p-chlorophenyl)biguandino)hexane
1,6-Bis(p-chlorophenyldiguanido)hexane
1,6-Di(4-chlorophenyldiguanido)hexane
2,4,11,13-Tetraazatetradecanediimidamide, N,N-bis(4-chlorophenyl)-3,12-diimino-
4-12-00-01201 (Beilstein Handbook Reference)
BRN 2826432
Chlorhexidin
Chlorhexidine
Chlorhexidinum
Cloresidina
Clorhexidina
EINECS 200-238-7
Fimeil
Hexadol
Nolvasan
Rotersept
Soretol
Sterilon
Tubulicid
ATC A01AB03
B05CA02
D08AC02
D09AA12
G04BX14
R02AA05
S01AX09
S02AA09
S03AA04
CID 9552079
CAS 000055561
TTD Drug ID DAP001326
SMILES ClC1=CC=C(NC(=N)NC(=N)NCCCCCCNC(=N)NC(=N)NC2=CC=C(Cl)C=C2)C=C1
Formula C22H30Cl2N10
Molweight 505.447
Atoms 34
LogP 6.2838
Rotatable Bonds 13
H-Bond Donors 6
H-Bond Acceptors 10
Phase2 interactions
NameReferences
MET 3337739
Transporter
AC-No.NameReferences
P19634Sodium/hydrogen exchanger 1 16179939
Q86UG4Cancer/testis antigen 48 9439681
Amphotericin B

Java required.


Information Structure
Name Amphotericin B
Synonyms
(1R-(1R*,3S*,5R*,6R*,9R*,11R*,15S*,16R*,17R*,18S*,19E,21E,23E,25E,27E,29E,31E,33R*,35S*,36R*,37S*))-33-((3-Amino-3,6-dideoxy-beta-D-mannopyranosyl)oxy
14,39-Dioxabicyclo(33.3.1)nonatriaconta-19,21,23,25,2 7,29,31-heptaene-36-carboxylic Acid, 33-((3-amino-3,6-dideoxy-beta-D-mannopyranosyl)oxy)-1,3,5,6
5-18-10-00525 (Beilstein Handbook Reference)
Abelcet
ABLC
AI3-26528
Ambisome
Amfotericina B
Ampho-Moronal
Amphocin
Amphomoronal
Amphotericin B
AmphotericinB
Amphotericine B
Amphotericinum B
Amphozone
BRN 0078342
BU2690300
CCRIS 5963
component Of Talsutin
DRG-0096
EINECS 215-742-2
Fungilin
Fungizone
HSDB 3008
IAB
Liposomal Amphotericin B
Mysteclin-F
NS 718
NSC 527017
Tegopen
ATC A01AB04
A07AA07
D01AA10
G01AA03
J02AA01
CID 14956
CAS 001397893
TTD Drug ID DAP001322
SMILES C[C@H]1O[C@@H](O[C@@H]2C[C@@H]3O[C@](O)(C[C@@H](O)C[C@@H](O)[C@H](O)CC[C@@H](O)C[C@@H](O)CC(=O)O[C@@H](C)[C@H](C)[C@H](O)[C@@H](C)C=CC=CC=CC=CC=CC=CC=C2)C[C@H](O)[C@H]3C(O)=O)[C@@H](O)[C@@H](N)[C@@H]1O
Formula C47H73NO17
Molweight 924.079
Atoms 83
LogP 1.412
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 18
Transporter
AC-No.NameReferences
P19634Sodium/hydrogen exchanger 1 16179939
Q86UG4Cancer/testis antigen 48 9439681
Extrarenal fraction 0.95
Elimination half-life 15 days
Polynoxylin

Java required.


Information Structure
Name Polynoxylin
Synonyms
Formaldehyde, Urea Polymer
Gabrite
Hygromull
Karbamol
Karbamol B/M
Kauresin K244
Kaurit 285 FL
Kaurit 420
KM 2 (Polymer)
Pianizol
Piatherm
Piatherm D
Plastopal BT
Plyamine HD 1129A
Plyamine P 364BL
Polynoxylin
Ponoxylan
PR 703-78
Resamin 155F
Resamin HW 505
Resina X
S-Resin AER 20
Uformite 700
Uformite F 240N
Uloid 100
Uloid 22
ATC A01AB05
D01AE05
CID 62705
CAS 009011056
SMILES NC(N)=O
Transporter
AC-No.NameReferences
P19634Sodium/hydrogen exchanger 1 16179939
Q86UG4Cancer/testis antigen 48 9439681
Domiphen

Java required.


Information Structure
Name Domiphen
Synonyms
Domiphen
ATC A01AB06
CID 3149
CAS x006
SMILES CCCCCCCCCCCCN(C)(C)CCOC1=CC=CC=C1
Transporter
AC-No.NameReferences
P19634Sodium/hydrogen exchanger 1 16179939
Q86UG4Cancer/testis antigen 48 9439681
Oxyquinoline

Java required.


Information Structure
Name Oxyquinoline
Synonyms
1-Azanaphthalene-8-ol
5-21-03-00252 (Beilstein Handbook Reference)
8-Chinolinol
8-Hydroxy-chinolin
8-Hydroxychinolin
8-Hydroxyquinoline
8-OQ
8-Oxyquinoline
8-Quinol
8-Quinolinol
AI3-00483
Bioquin
BRN 0114512
Caswell No. 719
CCRIS 340
EINECS 205-711-1
EPA Pesticide Chemical Code 059803
Fennosan
Fennosan H 30
Fennosan HF-15
HSDB 4073
Hydroxybenzopyridine
NCI-C55298
NSC 2039
o-Oxychinolin
Oxin
Oxine
Oxybenzopyridine
Oxychinolin
Oxyquinoline
Phenopyridine
Quinoline, 8-hydroxy-
Quinophenol
Tumex
USAF EK-794
ATC A01AB07
D08AH03
G01AC30
R02AA14
CID 1923
CAS 000148243
SMILES OC1=CC=CC2=C1N=CC=C2
Formula C9H7NO
Molweight 145.158
Atoms 11
LogP 1.9404
Rotatable Bonds 0
H-Bond Donors 0
H-Bond Acceptors 2
Transporter
AC-No.NameReferences
P19634Sodium/hydrogen exchanger 1 16179939
Q86UG4Cancer/testis antigen 48 9439681
Neomycin

Java required.


Information Structure
Name Neomycin
Synonyms
Caswell No. 595
CCRIS 5462
EINECS 215-766-3
EPA Pesticide Chemical Code 006303
Fradiomycin
Fradiomycinum
HSDB 3242
Myacyne
Mycifradin
Neolate
Neomas
Neomcin
Neomicina
Neomin
Neomycin
Neomycine
Neomycinum
Nivemycin
Vonamycin Powder V
ATC A01AB08
A07AA01
B05CA09
D06AX04
G01AA14
J01GB05
R02AB01
S01AA03
S02AA07
S03AA01
CID 8378
CAS 001404042
Drugbank ID DB00994
TTD Drug ID DPR000037
SMILES NC[C@H]1O[C@H](O[C@@H]2[C@@H](N)C[C@@H](N)[C@H](O)[C@H]2O[C@@H]3O[C@H](CO)[C@@H](O[C@H]4O[C@@H](CN)[C@@H](O)[C@H](O)[C@H]4N)[C@H]3O)[C@H](N)[C@@H](O)[C@@H]1O
Formula C23H46N6O13
Molweight 614.644
Atoms 42
LogP -4.6935
Rotatable Bonds 9
H-Bond Donors 0
H-Bond Acceptors 19
Transporter
AC-No.NameReferences
P14672Solute carrier family 2, facilitated glucose transporter member 4 11500317
Extrarenal fraction 0.05
Elimination half-life 2h
Miconazole

Java required.


Information Structure
Name Miconazole
Synonyms
1-(2,4-Dichloro-beta-((2,4-dichlorobenzyl)oxy)phenethyl)imidazole
5-23-04-00320 (Beilstein Handbook Reference)
BRN 0965511
CCRIS 7924
Daktarin IV
EINECS 245-324-5
Miconazol
Miconazole
Miconazolo
Miconazolum
MJR 1762
Monistat IV
NSC 170986
R 18134
ATC A01AB09
A07AC01
D01AC02
G01AF04
J02AB01
S02AA13
CID 4189
CAS 022916478
Drugbank ID DB01110
TTD Drug ID DAP000154
SMILES ClC1=CC=C(CO[C@H](CN2C=CN=C2)C3=CC=C(Cl)C=C3Cl)C(Cl)=C1
Formula C18H14Cl4N2O
Molweight 416.129
Atoms 25
LogP 6.4548
Rotatable Bonds 6
H-Bond Donors 0
H-Bond Acceptors 2
CYP interactions
NameRelationsReferences
1A2Inhibitor 16141569
16141569
2A6Inhibitor 9143352
2B6Inhibitor 11854151
2C9Inhibitor 16141567
10945865
10709776
16141567
2C19Inhibitor 16141567
11854151
16141567
2D6Inhibitor 16141569
11854151
16141569
2E1Inhibitor 16141569
16141569
3A4Substrate Inhibitor 15135088
11996015
11B1Inhibitor 7663533
19AInhibitor 15554355
Transporter
AC-No.NameReferences
P14672Solute carrier family 2, facilitated glucose transporter member 4 11500317
Extrarenal fraction 1
Elimination half-life 24h
Natamycin

Java required.


Information Structure
Name Natamycin
Synonyms
16-(3-Amino-3,6-didesoxy-beta-D-mannopyranosyloxy)-5,6-epoxy-8,12,14-trihydroxy-26-methyl-2,10-dioxo-1-oxacyclohexacosa-3,17,19,21,23-pentaen-13-carbo
Antibiotic A-5283
CL 12,625
CL 12625
Delvocid
Delvolan
Delvopos
EINECS 231-683-5
Mycophyt
Myprozine
Natacyn
Natafucin
Natamicina
Natamycin
Natamycine
Natamycinum
Pimafucin
Pimaricine
Pimarizin
Stereoisomer Of 22-((3-amino-3,6-dideoxy-beta-D-mannopyranosyl)oxy)-1,3,26-trihydroxy-12-methyl-10-oxo-6,11,28-trioxatricyclo(22.3.1.0(sup 5,7))octaco
Synogil
Tennecetin
ATC A07AA03
D01AA02
G01AA02
S01AA10
A01AB10
CID 5281099
CAS 007681938
Drugbank ID DB00826
TTD Drug ID DAP001331
SMILES C[C@@H]1CC=CC=CC=CC=C[C@H](C[C@H]2O[C@](O)(C[C@@H](O)C[C@H]3O[C@@H]3C=CC(=O)O1)C[C@H](O)[C@@H]2C(O)=O)O[C@@H]4O[C@@H](C)[C@@H](O)[C@H](N)[C@@H]4O
Formula C33H47NO13
Molweight 665.725
Atoms 70
LogP 0.82
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 14
Transporter
AC-No.NameReferences
P14672Solute carrier family 2, facilitated glucose transporter member 4 11500317
Hexetidine

Java required.


Information Structure
Name Hexetidine
Synonyms
1,3-Bis(2-ethylhexyl)hexahydro-5-methyl-5-pyrimidiamine
5-Amino-1,3-bis(2-ethylhexyl)-5-methyl-hexhydropyrimidine
5-Amino-1,3-bis(2-ethylhexyl)-5-methylhexahydropyrimidine
5-Pyrimidinamine, 1,3-bis(2-ethylhexyl)hexahydro-5-methyl-
AI3-15546
Caswell No. 033BB
Collu Hextril
Duranil Aerosol
EINECS 205-513-5
Elsix
Glypesin
Hexetidin
Hexetidina
Hexetidine
Hexetidinum
Hexoral
Hextril
NSC 17764
Oraldene
P 252
Steri/Sol (VAN)
Sterilate
Sterisil
Triocil
Triscol
ATC A01AB12
G01AX22
R02AA28
CID 3607
CAS 000141946
SMILES CCCC[C@@H](CC)CN1CN(C[C@H](CC)CCCC)C[C@](C)(N)C1
Formula C21H45N3
Molweight 339.602
Atoms 24
LogP 5.2878
Rotatable Bonds 12
H-Bond Donors 0
H-Bond Acceptors 3
Transporter
AC-No.NameReferences
P14672Solute carrier family 2, facilitated glucose transporter member 4 11500317
Tetracycline

Java required.


Information Structure
Name Tetracycline
Synonyms
(4S,4aS,5aS,12aS)-4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide
2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-6-methyl-1,11-dioxo-
4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,1 0,12,12a-pentahydroxy-6-methyl-1,11-dioxo-2-naphthacenecarboxamide
6-Methyl-1,11-dioxy-2-naphthacenecarboxamide
Abramycin
Abricycline
Achromycin
Achromycin (naphthacene Derivative)
Agromicina
Ambramicina
Ambramycin
Amycin
Bio-tetra
Biocycline
Cefracycline
Cefracycline Suspension
Centet (base)
Ciclibion
Copharlan
Criseociclina
Cyclomycin
Cyclopar
Democracin
Deschlorobiomycin
EINECS 200-481-9
Hostacyclin
HSDB 3188
Lexacycline
Limecycline
Liquamycin (Veterinary)
Mericycline
Micycline
Neocycline
NSC 108579
Omegamycin
Orlycycline
Panmycin
Piracaps (base)
Polycycline
Polycycline (antibiotic)
Polycycline (VAN)
Polyotic
Purocyclina
Robitet
Roviciclina
SK-Tetracycline
Solvocin
Sumycin
Sumycin Syrup
T-125
Tetra-co
Tetrabon
Tetraciclina
Tetracycl
Tetracyclin
Tetracycline
Tetracycline I
Tetracycline II
Tetracyclinum
Tetracyn
Tetradecin
Tetrafil
Tetraverine
Tsiklomistsin
Tsiklomitsin
Veracin
Vetacyclinum
Vetquamycin-324 (free Base)
ATC A01AB13
D06AA04
D10AF05
J01AA07
S01AA09
S02AA08
S03AA02
CID 5280962
CAS 000060548
Drugbank ID DB00759
TTD Drug ID DAP001527
SMILES CN(C)[C@H]1[C@@H]2C[C@@H]3C(=C(O)[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)C4=C(O)C=CC=C4[C@@]3(C)O
Formula C22H24N2O8
Molweight 444.435
Atoms 32
LogP 0.3293
Rotatable Bonds 1
H-Bond Donors 6
H-Bond Acceptors 10
CYP interactions
NameRelationsReferences
3A4Substrate Inhibitor 9384469
umm
9399990
9384469
Phase2 interactions
NameReferences
GST 11807801
Transporter
AC-No.NameReferences
Q86UG4SLCO6A1 11807801
Extrarenal fraction 0.12
Elimination half-life 6h
Benzoxonium Chloride

Java required.


Information Structure
Name Benzoxonium chloride
Synonyms
Absonal
Absonal V
Bactofen
Beloran
Benzoxonii Chloridum
Benzoxonium Chloride
Benzylbis(2-hydroxyethyl)dodecyl Ammonium Chloride
Benzyldodecylbis(2-hydroxyethyl)ammonium Chloride
Benzyldodecyldiethanolammonium Chloride
Bialcol
Bis(2-hydroxyethyl)benzyl-n-dodecylammonium Chloride
Bis(2-hydroxyethyl)benzyldodecylammonium Chloride
Bradophen
Caswell No. 416A
Chlorure De Benzoxonium
Cloruro De Benzoxonio
Cohortan
D 301
D301
Di(2-hydroxyethyl)benzyldodecylammonium Chloride
Dodecyl Di(2-hydroxyethyl) Benzyl Ammonium Chloride
Dodecyl(benzyl)diethanolammonium Chloride
Dodecyl(dioxyethyl)benzylammonium Chloride
Dodecyl-di(beta-oxyaethyl)-benzyl-ammoniumchlorid
Dodecylbis(2-hydroxyethyl)benzylammonium Chloride
Dodecylbis(beta-hydroxyethyl)benzylammonium Chloride
Dodecyldi(2-hydroxyethyl)benzylammonium Chloride
Dodecyldi(beta-hydroxyethyl)benzylammonium Chloride
EINECS 243-008-1
EPA Pesticide Chemical Code 069181
Katanol C12
Laurylbis(2-hydroxyethyl)benzylammonium Chloride
Lomades
N-Dodecyl-N,N-bis(2-hydroxyethyl)benzenemethanaminium Chloride
NSC 141905
Orofar
ZY 15021
ATC A01AB14
D08AJ05
CID 29563
CAS 019379909
SMILES CCCCCCCCCCCC[N+](CCO)(CCO)CC1=CC=CC=C1
Formula C23H42ClNO2
Molweight 400.038
Atoms 27
LogP 1.9129
Rotatable Bonds 17
H-Bond Donors 0
H-Bond Acceptors 2
Transporter
AC-No.NameReferences
Q86UG4SLCO6A1 11807801
Tibezonium Iodide

Java required.


Information Structure
Name Tibezonium iodide
Synonyms
2-(beta-(N-Diethylamino)ethylthio)-4-(p-phenylthio)phenyl-3H-1,5-benzodiazepine Methiodide
EINECS 259-284-1
Iodure De Tibezonium
Ioduro De Tibezonio
NSC 308905
REC-15/0691
Thiabenzazonium
Thiabenzazonium Iodide
Tibenzonio Ioduro
Tibenzonium Iodide
Tibezonii Iodidum
Tibezonium Iodide
ATC A01AB15
CID 6918582
CAS 054663477
SMILES CC[N+](C)(CC)CCSC1=CC(=NC2=C(N1)C=CC=C2)C3=CC=C(SC4=CC=CC=C4)C=C3
Formula C28H32IN3S2
Molweight 601.608
Atoms 34
LogP 3.4871
Rotatable Bonds 9
H-Bond Donors 0
H-Bond Acceptors 2
Transporter
AC-No.NameReferences
Q86UG4SLCO6A1 11807801
Mepartricin

Java required.


Information Structure
Name Mepartricin
Synonyms
Ipertrofan
Mepartricin
Mepartricina
Mepartricine
Mepartricinum
Methylpartricin
Orofungin
SN654
Spa-S-160
Tricandil
Tricangine
ATC A01AB16
D01AA06
G01AA09
G04CX03
CID 56842231
CAS 011121327
SMILES COC(=O)[C@H]1[C@@H](O)C[C@@]2(O)C[C@@H](O)C[C@@H](O)C[C@H](O)C[C@@H](O)CC(=O)C[C@@H](O)CC(=O)O[C@@H]([C@H](C)CC[C@H](O)CC(=O)C3=CC=C(N)C=C3)[C@@H](C)C=CC=CC=CC=CC=CC=CC=C[C@@H](C[C@@H]1O2)O[C@@H]4O[C@H](C)[C@@H](O)[C@H](N)[C@@H]4O
Transporter
AC-No.NameReferences
Q86UG4SLCO6A1 11807801
Metronidazole

Java required.


Information Structure
Name Metronidazole
Synonyms
1-(2-Hydroxy-1-ethyl)-2-methyl-5-nitroimidazole
1-(2-Hydroxyethyl)-2-methyl-5-nitroimidazole
1-(beta-Ethylol)-2-methyl-5-nitro-3-azapyrrole
1-(beta-Hydroxyethyl)-2-methyl-5-nitroimidazole
1-(beta-Oxyethyl)-2-methyl-5-nitroimidazole
2-Methyl-1-(2-hydroxyethyl)-5-nitroimidazole
2-Methyl-3-(2-hydroxyethyl)-4-nitroimidazole
2-Methyl-5-nitroimidazole-1-ethanol
5-23-05-00063 (Beilstein Handbook Reference)
Acromona
Anagiardil
Arilin
Atrivyl
Bayer 5360
Bexon
BRN 0611683
Caswell No. 579AA
CCRIS 410
Clont
CONT
Danizol
Deflamon
Deflamon-wirkstoff
Efloran
EINECS 207-136-1
Elyzol
Entizol
EPA Pesticide Chemical Code 120401
Eumin
Flagemona
Flagesol
Flagil
Flagyl
Fossyol
Giatricol
Gineflavir
HSDB 3129
Klion
Klont
Meronidal
Metro Gel
Metro I.V.
Metronidaz
Metronidazol
Metronidazole
Metronidazolo
Metronidazolum
Mexibol
Mexibol Silanes
Monagyl
Monasin
Nalox
Neo-tric
NIDA
Noritate
Novonidazol
NSC-50364
Orvagil
Protostat
RP 8823
Sanatrichom
Satric
SC 10295
Takimetol
Trichazol
Trichex
Trichocide
Trichomol
Trichomonacid Pharmachim
Trichopol
Tricocet
Tricom
Tricowas B
Trikacide
Trikamon
Trikojol
Trikozol
Trimeks
Trivazol
Vagilen
Vagimid
Vertisal
Wagitran
ATC A01AB17
D06BX01
G01AF01
J01XD01
P01AB01
CID 4173
CAS 000443481
Drugbank ID DB00916
TTD Drug ID DAP000534
SMILES CC1=NC=C(N1CCO)[N+]([O-])=O
Formula C6H9N3O3
Molweight 171.154
Atoms 12
LogP 0.6152
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 4
CYP interactions
NameRelationsReferences
2C8Inhibitor umm
2C9Substrate Inhibitor 15038460
umm
11996015
3A4Substrate Inhibitor 15038460
umm
11151744
8877250
9469685
17374625
Transporter
AC-No.NameReferences
Q86UG4SLCO6A1 11807801
Extrarenal fraction 0.85
Elimination half-life 7h
Clotrimazole

Java required.


Information Structure
Name Clotrimazole
Synonyms
(2-Chlorophenyl)diphenyl-1-imidazolylmethane
(Chlorotrityl)imidazole
1-((2-Chlorophenyl)diphenylmethyl)-1H-imidazole
1-((o-Chloro-phenyl)diphenylmethyl)imidazole
1-(alpha-(2-Chlorophenyl)benzhydryl)imidazole
1-(o-Chloro-alpha,alpha-diphenylbenzyl)imidazole
1-(o-Chlorophenyldiphenylmethyl)imidazole
1-(o-Chlorotrityl)imidazole
1H-Imidazole, 1-((2-chlorophenyl)diphenylmethyl)-
5-23-04-00291 (Beilstein Handbook Reference)
B 5097
BAY 5097
BAY B 5097
Bay-B 5097
Bis-fenil-(2-clorofenil)-1-imidazolil-metano
Bis-phenyl-(2-chlorophenyl)(1-imidazoyl)methane
Bisphenyl-(2-chlorphenyl)-1-imidazolyl-methan
BRN 0622318
Canesten
Canestine
CCRIS 6245
Chlotrimazole
Clotrimazol
Clotrimazole
Clotrimazolum
Desamix F
Diphenyl(2-chlorophenyl)(1-imidazolyl)methane
Diphenyl-(2-chlorophenyl)-1-imidazolylmethane
DRG-0072
EINECS 245-764-8
Empecid
FB 5097
Fem Care
Gyne Lotrimin
Gyne-Lotrimin
HSDB 3266
Lotrimin
Lotrimin AF Cream
Lotrimin AF Jock-Itch Cream
Lotrimin AF Solution
Methane, Bis-phenyl-(2-chlorophenyl)-1-imidazolyl-
Mycelex
Mycelex 7
Mycelex G
Mycelex OTC
Mycelex Troches
Mycosporin
Mykosporin
NSC 257473
Trimysten
Veltrim
ATC A01AB18
D01AC01
G01AF02
CID 2812
CAS 023593751
Drugbank ID DB00257
TTD Drug ID DAP000138
SMILES ClC1=C(C=CC=C1)C(N2C=CN=C2)(C3=CC=CC=C3)C4=CC=CC=C4
Formula C22H17ClN2
Molweight 344.837
Atoms 25
LogP 5.3767
Rotatable Bonds 4
H-Bond Donors 0
H-Bond Acceptors 1
CYP interactions
NameRelationsReferences
1A2Inhibitor umm
2A6Inhibitor Inducer 1472091
umm
9143352
2B6Inhibitor Inducer umm
14977870
2C8Inhibitor 11136296
11136296
15601807
2C9Inhibitor 11996015
2C19Inhibitor umm
2D6Inhibitor umm
2E1Inhibitor 9574817
15135088
umm
3A4Inhibitor Inducer 12867495
umm
12538830
15135088
3A7Inducer 12673034
11B1Inhibitor 7663533
19AInhibitor 15554355
Transporter
AC-No.NameReferences
P33527Multidrug resistance-associated protein 111737211
Q92887Canalicular multispecific organic anion transporter 111836020
Sodium Perborate

Java required.


Information Structure
Name Sodium perborate
Synonyms
Dexol
EINECS 231-556-4
HSDB 1676
Perboric Acid (HBO(O2)), Sodium Salt
Perboric Acid (HBO3), Sodium Salt
Perboric Acid, Sodium Salt
Sodium Perborate
Sodium Perborate (BaBO3)
Sodium Peroxoborate
ATC A01AB19
CID 517072
CAS 007632044
SMILES [O-]OB=O
Formula BHNaO3
Molweight 82.8069
Atoms 5
LogP -0.9545
Rotatable Bonds 1
H-Bond Donors 0
H-Bond Acceptors 3
Transporter
AC-No.NameReferences
P33527Multidrug resistance-associated protein 111737211
Q92887Canalicular multispecific organic anion transporter 111836020
Chlortetracycline

Java required.


Information Structure
Name Chlortetracycline
Synonyms
7-Chlorotetracycline
Acronize
Aureocina
Aureomycin
Aureomycin A-377
Aureomykoin
Biomitsin
Biomycin
Biomycin A
Caswell No. 219B
Chlortetracycline
Chlortetracyclinum
Chrysomykine
Clortetraciclina
CTC
CTC (abtibiotic)
Duomycin
EINECS 200-341-7
EPA Pesticide Chemical Code 006301
Flamycin
Tri-chlortetracycline
Uromycin
ATC A01AB21
D06AA02
J01AA03
S01AA02
CID 5280963
CAS 000057625
TTD Drug ID DAP000881
SMILES CN(C)[C@H]1[C@@H]2C[C@@H]3C(=C(O)[C@]2(O)C(=O)C(C(N)=O)=C1O)C(=O)C4=C(O)C=CC(Cl)=C4[C@@]3(C)O
Formula C22H23ClN2O8
Molweight 478.88
Atoms 36
LogP 0.9827
Rotatable Bonds 1
H-Bond Donors 0
H-Bond Acceptors 10
Transporter
AC-No.NameReferences
P33527Multidrug resistance-associated protein 111737211
Q92887Canalicular multispecific organic anion transporter 111836020
Extrarenal fraction 0.8
Elimination half-life 6h
Doxycycline

Java required.


Information Structure
Name Doxycycline
Synonyms
2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methyl,1,11-dioxo-, (4S-(4alpha,4aalpha,5alpha
4-(Dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy- 6-methyl-1,11-dioxo-2-naphthacenecarboxamide Monohydrate
5-Hydroxy-alpha-6-deoxytetracycline
5-Hydroxy-alpha-6-deoxytetracycline Monohydrate
6-alpha-Deoxy-5-oxytetracycline
6-Deoxyoxytetracycline
6-Deoxytetracycline
6alpha-Deoxy-5-oxytetracycline
alpha-6-Deoxy-5-hydroxytetracycline
alpha-6-Deoxyoxytetracycline
alpha-6-Deoxyoxytetracycline Monohydrate
alpha-6-Tetracycline Monohydrate
alpha-Doxycycline
Azudoxat
Deoxymykoin
Dossiciclina
Doxiciclina
Doxitard
Doxivetin
Doxy-Caps
Doxy-Puren
Doxy-Tabs
Doxycen
Doxycycline
Doxycycline Anhydrous
Doxycyclinum
Doxytetracycline
EINECS 209-271-1
GS 3065
GS-3065
HSDB 3071
Investin
Liviatin
Monodox
Nordox
Oxytetracycline, 6-deoxy-
Ronaxan
Spanor
Vibra-Tabs
Vibramycin
Vibramycine
Vibravenos
ATC A01AB22
J01AA02
CID 5281011
CAS 000564250
Drugbank ID DB00254
TTD Drug ID DAP000399
SMILES C[C@@H]1[C@H]2[C@H](O)[C@H]3[C@H](N(C)C)C(O)=C(C(N)=O)C(=O)[C@@]3(O)C(O)=C2C(=O)C4=C(O)C=CC=C14
Formula C22H24N2O8
Molweight 444.435
Atoms 37
LogP 0.1961
Rotatable Bonds 1
H-Bond Donors 0
H-Bond Acceptors 10
CYP interactions
NameRelationsReferences
1B1Inhibitor 17365149
3A4Substrate Inhibitor umm
9384469
9399990
Transporter
AC-No.NameReferences
C9J2P6SLC41A216984228
C9JQG1SLC26A421965328
P55851UCP 2 17131143
Q9UNQ0ATP-binding cassette sub-family G member 218820913
Elimination half-life 16h
Minocycline

Java required.


Information Structure
Name Minocycline
Synonyms
2-Naphthacenecarboxamide, 4,7-bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-, (4S-(4alpha,4aalpha,5aalpha,12aa
4,7-Bis(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,10,12,12a-tetrahydroxy-1,11-dioxo-2-naphthacenecarboxamide
7-Dimethylamino-6-demethyl-6-deoxytetracycline
BRN 3077644
CL 59806
HSDB 3130
Minociclina
Minocyclin
Minocycline
Minocyclinum
ATC J01AA08
A01AB23
CID 5281021
CAS 010118908
TTD Drug ID DAP000405
SMILES CN(C)[C@H]1[C@@H]2C[C@@H]3CC4=C(C=CC(O)=C4C(=O)C3=C(O)[C@]2(O)C(=O)C(C(N)=O)=C1O)N(C)C
Formula C23H27N3O7
Molweight 457.476
Atoms 36
LogP 0.7303
Rotatable Bonds 2
H-Bond Donors 0
H-Bond Acceptors 9
Transporter
AC-No.NameReferences
C9J2P6SLC41A216984228
C9JQG1SLC26A421965328
P55851UCP 2 17131143
Q9UNQ0ATP-binding cassette sub-family G member 218820913
Extrarenal fraction 0.85
Elimination half-life 17h
Aluminiumchlorid

Java required.


Information Structure
Name Aluminiumchlorid
Synonyms
AI3-01917
Alluminio(cloruro Di)
Aluminium Chloride
Aluminium Trichloride
Aluminium, (chlorure D)
Aluminiumchlorid
Aluminum Chloride
Aluminum Chloride (1:3)
Aluminum Chloride Anhydrous
Aluminum Trichloride
Aluminum, (chlorure D)
Caswell No. 029
CCRIS 6871
Chlorure Daluminium
EINECS 231-208-1
EPA Pesticide Chemical Code 013901
HSDB 607
NSC 143015
NSC 143016
Pearsall
TK Flock
Trichloroaluminum
ATC A01AB26
D10AX01
CID 24012
CAS 007446700
SMILES Cl[Al](Cl)Cl
Transporter
AC-No.NameReferences
C9J2P6SLC41A216984228
C9JQG1SLC26A421965328
P55851UCP 2 17131143
Q9UNQ0ATP-binding cassette sub-family G member 218820913
Ethacridinlactat

Java required.


Information Structure
Name Ethacridinlactat
Synonyms
2,5-Diamino-7-ethoxyacridine Lactate
2-Aethoxy-6,9-diaminoacridinlactat
2-Ethoxy-6,9-diaminoacridine Lactate
2-Ethoxy-6,9-diaminoacridinium Lactate
2-Hydroxypropanoic Acid, Compd. With 7-ethoxy-3,9-acridinediamine (1:1)
3,9-Diamino-7-ethoxyacridinium Lactate
6,9-Acridinediamine, 2-ethoxy-, 2-hydroxypropanoate (1:1)
6,9-Diamino-2-ethoxyacridine Lactate
Acridine, 6,9-diamino-2-ethoxy-, Compd. With Lactic Acid (1:1)
Acridine, 6,9-diamino-2-ethoxy-, Lactate
Acridine, 6,9-diamino-2-ethoxy-, Monolactate
Acrinol
Acrinolum
Acrolactine
Akron
Amoebin
Antidiar 200
CCRIS 5165
EINECS 217-408-1
Ethacridine Lactate
Ethacridinlactat
Ethodin
Flavitrol
Hectalin
Metifex
NSC 36333
Rimaon
Rivanol
Rivinol
Vucine
ATC A01AB27
A07AX07
B05CA08
D08AA01
CID 2017
CAS 001837576
SMILES CCOC1=CC=C2N=C3C=C(N)C=CC3=C(N)C2=C1
Formula C15H15N3O
Molweight 253.299
Atoms 19
LogP 4.1135
Rotatable Bonds 2
H-Bond Donors 0
H-Bond Acceptors 4
Transporter
AC-No.NameReferences
C9J2P6SLC41A216984228
C9JQG1SLC26A421965328
P55851UCP 2 17131143
Q9UNQ0ATP-binding cassette sub-family G member 218820913
Natriumhypochlorit

Java required.


Information Structure
Name Natriumhypochlorit
Synonyms
AD Gel
Antiformin
B-K Liquid
Carrel-dakin Solution
Caswell No. 776
CCRIS 708
Chloros
Chlorox
Cloralex
Cloropool
Clorox
Clorox Liquid Bleach
Dakins Solution
Deosan
Deosan Green Label Steriliser
Dispatch
EINECS 231-668-3
EPA Pesticide Chemical Code 014703
Hospital Milton
Household Bleach
HSDB 748
Hyclorite
Hypochlorite Sodium
Hyposan And Voxsan
Hypure
Hypure N
Javel Water
Javelle Water
Javex
Klorocin
Milton
Milton Crystals
Modified Dakins Solution
Natriumhypochlorit
Neo-cleaner
Neoseptal CL
Parozone
Purin B
Sodium Hypochlorite
Sodium Hypochlorite (NaClO)
Sodium Hypochlorite (NaOCl)
Sodium Oxychloride
Solutions, Dakins
Sunnysol 150
Surchlor
UN 1791
XY 12
Youxiaolin
ATC A01AB31
D08AX07
CID 23665760
CAS 007681529
SMILES [O-]Cl
Formula ClNaO
Molweight 74.4422
Atoms 3
LogP 0.5707
Rotatable Bonds 0
H-Bond Donors 0
H-Bond Acceptors 1
Transporter
AC-No.NameReferences
C9J2P6SLC41A216984228
C9JQG1SLC26A421965328
P55851UCP 2 17131143
Q9UNQ0ATP-binding cassette sub-family G member 218820913
Nystatin

Java required.


Information Structure
Name Nystatin
Synonyms
AI3-26526
Biofanal
Candex Lotion
Candio-hermal
Caswell No. 607B
Diastatin
DRG-0064
EINECS 215-749-0
EPA Pesticide Chemical Code 202800
Fungicidin
Herniocid
HSDB 3138
Korostatin
Moronal
Moronal (antibiotic)
Myconystatin
Mycostatin
Mycostatin 20
Mycostatin Pastilles
Mykostatyna
Nilstat
Nistatin
Nistatina
Nyotran
Nystan
Nystatin
Nystatin A1, A2, A3 Complex
Nystatin LF (liposome)
Nystatine
Nystatinum
Nystatyna
Nystavescent
Nystex
O-V Statin
Stamycin
Zydin E
ATC A01AB33
A07AA02
D01AA01
G01AA01
CID 11953884
CAS 001400619
Drugbank ID DB00646
TTD Drug ID DAP000879
SMILES C[C@@H]1OC(=O)C[C@H](O)C[C@H](O)C[C@@H](O)CC[C@H](O)[C@H](O)C[C@]2(O)C[C@H](O)[C@H]([C@H](C[C@H](O[C@H]3O[C@H](C)[C@@H](O)[C@H](N)[C@@H]3O)C=CC=CC=CC=CCCC=CC=C[C@H](C)[C@@H](O)[C@H]1C)O2)C(O)=O
Formula C47H75NO17
Molweight 926.095
Atoms 95
LogP 1.4786
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 18
Transporter
AC-No.NameReferences
C9J2P6SLC41A216984228
C9JQG1SLC26A421965328
P55851UCP 2 17131143
Q9UNQ0ATP-binding cassette sub-family G member 218820913