Compound - Results

Fusidic Acid

Java required.


Information Structure
Name Fusidic acid
Synonyms
3alpha,11alpha,16beta-Trihydroxy-29-nor-8alpha,9beta,13alpha,14beta-dammara-17(20),24-dien-21-oic Acid 16-acetate
Acide Fusidique
Acido Fusidico
Acidum Fusidicum
C.A.S. 62,602; Diethanolamine Fusidate
EINECS 230-256-0
Fucidic Acid
FUCIDIN
Fucidin Acid
Fusidic Acid
Fusidine
NSC 56192
Ramycin
SQ 16603
ATC D06AX01
D09AA02
J01XC01
S01AA13
CID 3000226
CAS 006990063
Drugbank ID DB02703
TTD Drug ID DAP001008
SMILES C[C@@H]1[C@H](O)CC[C@@]2(C)[C@H]1CC[C@@]3(C)[C@@H]2[C@H](O)C[C@H]4C([C@H](C[C@]34C)OC(C)=O)=C(/CCC=C(/C)C)C(O)=O
Formula C31H48O6
Molweight 516.709
Atoms 44
LogP 5.6661
Rotatable Bonds 6
H-Bond Donors 0
H-Bond Acceptors 6
Extrarenal fraction 1
Elimination half-life 6h
Chloramphenicol

Java required.


Information Structure
Name Chloramphenicol
Synonyms
4-13-00-02742 (Beilstein Handbook Reference)
AI3-25003
Alficetyn
Ambofen
Amphenicol
Amphicol
Amseclor
Anacetin
Aquamycetin
Austracil
Austracol
Biocetin
Biophenicol
BRN 2225532
CAF
CAF (pharmaceutical)
CAM
CAP
Catilan
CCRIS 3922
Chemicetin
Chemicetina
Chlomin
Chlomycol
Chlora-tabs
Chloramex
Chloramfenikol
Chloramficin
Chloramfilin
Chloramphenicol
Chloramphenicol Crystalline
Chloramphenicol, D-
Chloramphenicolum
Chloramsaar
Chlorasol
Chlorbiotic (Veterinary)
Chloricol
Chlornitromycin
Chloro-25 Vetag
Chloroamphenicol
Chlorocaps
Chlorocid
Chlorocid S
Chlorocide
Chlorocidin C
Chlorocidin C Tetran
Chlorocol
Chloroject L
Chloromax
Chloromycetin
Chloromycetny
Chloronitrin
Chloroptic
Chloroptic S.O.P.
Chlorovules
Cidocetine
Ciplamycetin
Cloramfenicol
Cloramfenicolo
Cloramficin
Cloramicol
Cloramidina
Cloroamfenicolo
Clorocyn
Cloromisan
Clorosintex
Comycetin
CPh
Cylphenicol
D-(-)-2,2-Dichloro-N-(beta-hydroxy-alpha-(hydroxymethyl)-p-nitrophenylethyl)acetamide
D-(-)-Chloramphenicol
D-(-)-threo-1-(4-Nitrophenyl)-2-dichloroacetamido-1,3-propanediol
D-(-)-threo-1-p-Nitrophenyl-2-dichloracetamido-1,3-propanediol
D-(-)-threo-1-p-Nitrophenyl-2-dichloroacetylamino-1,3-propanediol
D-(-)-threo-2-Dichloroacetamido-1-p-nitrophenyl-1,3-propanediol
D-(-)-threo-Chloramphenicol
D-Chloramphenicol
D-threo-(1R,2R)-1-p-Nitrophenyl-2-dichloroacetamido-1,3-propanediol
Desphen
Detreomycin
Detreomycine
Dextromycetin
Doctamicina
Econochlor
EINECS 200-287-4
Embacetin
Emetren
Enicol
Enteromycetin
Erbaplast
Ertilen
Farmicetina
Fenicol
Globenicol
Glorous
Halomycetin
Hortfenicol
HSDB 3027
I 337A
Intramycetin
Isicetin
Ismicetina
Isophenicol
Isopto Fenicol
Juvamycetin
Kamaver
Kemicetina
Kemicetine
Klorita
Klorocid S
Laevomycetinum
Leukomyan
Leukomycin
Levomicetina
Levomitsetin
Levomycetin
Loromisin
Mastiphen
Mediamycetine
Medichol
Micloretin
Micochlorine
Micoclorina
Microcetina
Mychel
Mychel-Vet
Mycinol
NCI-C55709
Normimycin V
Novochlorocap
Novomycetin
Novophenicol
NSC 3069
Oftalent
Oleomycetin
Opclor
Ophthochlor
Otachron
Otophen
Pantovernil
Paraxin
Pentamycetin
Quemicetina
Rivomycin
Romphenil
Ronphenil
Septicol
Sificetina
Sintomicetina
Sintomicetine R
Sno-Phenicol
Stanomycetin
Synthomycetin
U-6062
ATC D06AX02
D10AF03
G01AA05
J01BA01
S01AA01
S02AA01
S03AA08
CID 5959
CAS 000056757
SMILES OC[C@@H](NC(=O)C(Cl)Cl)[C@H](O)C1=CC=C(C=C1)[N+]([O-])=O
Formula C11H12Cl2N2O5
Molweight 323.129
Atoms 22
LogP 1.8231
Rotatable Bonds 7
H-Bond Donors 0
H-Bond Acceptors 6
CYP interactions
NameRelationsReferences
2C8Inhibitor umm
2C9Inhibitor umm
9469685
11996015
2C19Substrate Inhibitor 14576103
medicine.iupui.edu/flockhart
14576103
3A4Inhibitor 14576103
14576103
Extrarenal fraction 0.95
Elimination half-life 4h
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
Bacitracin

Java required.


Information Structure
Name Bacitracin
Synonyms
AI3-50147-X
Ak-Tracin
Altracin
Ayfivin
Baci-Jel
Baciguent
Baciliquin
Bacitek Ointment
Bacitracin
Bacitracin-Neomycin-Polymyxin Ointment
Bacitracina
Bacitracine
Bacitracinum
Bactine Triple Antibiotic
Campho-Phenique Triple Plus Pain Reliever
EINECS 215-786-2
Fortracin
HSDB 6418
Mycitracin Plus Pain Reliever
Mycitracin Triple Antibiotic First Aid Ointment Maximum Strength
Parentracin
Penitracin
Septa
Spectrocin Plus
Topitracin
Topitrasin
USAF CB-7
Zutracin
ATC D06AX05
R02AB04
J01XX10
CID 2283
CAS 001405874
SMILES CC[C@H](C)[C@H](N)C1=N[C@@H](CS1)C(=O)N[C@@H](CC(C)C)C(=O)N[C@H](CCC(O)=O)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@H]2CCCCNC(=O)[C@H](CC(N)=O)NC(=O)[C@@H](CC(O)=O)NC(=O)[C@H](CC3=CNC=N3)NC(=O)[C@@H](CC4=CC=CC=C4)NC(=O)[C@@H](NC(=O)[C@@H](CCCN)NC2=O)[C@@H](C)CC
Formula C66H103N17O16S
Molweight 1422.69
Atoms 100
LogP 3.7241
Rotatable Bonds 39
H-Bond Donors 0
H-Bond Acceptors 33
Transporter
AC-No.NameReferences
Q8WWH1ATP-binding cassette transporter 21306428
Gentamicin

Java required.


Information Structure
Name Gentamicin
Synonyms
Cidomycin
EINECS 215-765-8
Garamycin
Garasol
Gentacycol
Gentamicin
Gentamicina
Gentamicine
Gentamicinum
Gentamycin
Gentamycin-creme
Gentamycinum
Gentavet
Gentocin
HSDB 3087
Refobacin
Refobacin TM
Uromycine
ATC D06AX07
J01GB03
S01AA11
S02AA14
S03AA06
CID 3467
CAS 001403663
Drugbank ID DB00798
TTD Drug ID DAP000116
SMILES CN[C@H](C)[C@@H]1CC[C@H](N)[C@H](O1)O[C@@H]2[C@@H](N)C[C@H](N)[C@H](O[C@H]3OC[C@](C)(O)[C@@H](NC)[C@@H]3O)[C@H]2O
Formula C21H43N5O7
Molweight 477.595
Atoms 33
LogP -0.4448
Rotatable Bonds 7
H-Bond Donors 0
H-Bond Acceptors 12
Transporter
AC-No.NameReferences
Q92887Canalicular multispecific organic anion transporter 116757538
Extrarenal fraction 0.02
Elimination half-life 3h
Tyrothricin

Java required.


Information Structure
Name tyrothricin
Synonyms
-d-leu-trp-d-leu-trp-d-leu-trp-nhch2ch2oh) Gramicidin A
1404-88-2
3-[(3r,6s,9s,12s,15s,17s,20s,22r,25s,28s)-20-(2-amino-2-oxoethyl)-9-(3-aminopropyl)-3,22,25-tribenzyl-15-[(4-hydroxyphenyl)methyl]-6-(2-methylpropyl)-
ac1l9qdm
an Antibacterial Substance Produced By The Growth Of Bacillus Brevis Dubos (fam. Bacteriaceae)
bactratycin
biothricin
caswell No. 900a
chembl577736
cid452550
coltirot
cyclic (-val-orn-leu-d-phe-pro-phe-d-phe-asn-glu-tyr-) Tyrocidine A & (hco-val-gly-ala-d-leu-ala-d-val-val-d-val-trp-d-leu-trp-d-leu-trp-d-leu-trp-nhc
dermotricine
dubos Crude Crystals
einecs 215-771-0
epa Pesticide Chemical Code 006311
ginotricina
gramicidin A & Tyrocidine A
hydrotricine
intraderm Tyrothricin
ls-158334
martricin
mixture Name
otalgine
pharothricetten
rinotricina
solutricine
tirotricina
tirotricina [inn-spanish]
triciderm
tyrex
tyri 10
tyroderm
tyrosur
tyrothricin
tyrothricin [inn:ban]
tyrothricine
tyrothricine [inn-french]
tyrothricinum
tyrothricinum [inn-latin]
tyrozets
ATC D06AX08
R02AB02
S01AA05
CID 452550
CAS cid452550
Drugbank ID DB00741
Formula C21H43N5O7
Molweight 477.595
Atoms 33
LogP -0.4448
Rotatable Bonds 7
H-Bond Donors 0
H-Bond Acceptors 12
Transporter
AC-No.NameReferences
Q92887Canalicular multispecific organic anion transporter 116757538
Mupirocin

Java required.


Information Structure
Name Mupirocin
Synonyms
(E)-(2S,3R,4R,5S)-5-((2S,3S,4S,5S)-2,3-Epoxy-5-hydroxy-4-methylhexyl)tetrahydro-3,4-dihydroxy-beta-methyl-2H-pyran-2-crotonic Acid, Ester With 9-hydro
8-Carboxyoctyl (E)-4-(2S,3R,4R,5S)-5-((2S,3S,4S,5S)-2,3-epoxy-5-hydroxy-4-methylhexyl)-3,4-dihydroxytetrahydro-2H-pyran-2-yl)-3-methylcrotonat
Bactroban
BRL 4910A
Mupirocin
Mupirocina
Mupirocine
Mupirocinum
Plasimine
Pseudomonic Acid
Pseudomonic Acid A
ATC D06AX09
R01AX06
CID 446596
CAS 012650690
Drugbank ID DB00410
TTD Drug ID DAP000711
SMILES C[C@H](O)[C@H](C)[C@@H]1O[C@H]1C[C@H]2CO[C@@H](CC(C)=CC(=O)OCCCCCCCCC(O)=O)[C@H](O)[C@@H]2O
Formula C26H44O9
Molweight 500.622
Atoms 44
LogP 2.5925
Rotatable Bonds 17
H-Bond Donors 0
H-Bond Acceptors 9
Transporter
AC-No.NameReferences
Q92887Canalicular multispecific organic anion transporter 116757538
Virginiamycin

Java required.


Information Structure
Name Virginiamycin
Synonyms
A Mixture Of Two Principal Antibiotic Components, Virginiamycin M1 (Factor M1) And Virginiamycin S1 (Factor S). Virginiamycin
Antibiotic No. 899
EINECS 234-244-6
Eskalin 500
Eskalin V
HSDB 7033
Micamicina
Mikamycin
Mikamycine
Mikamycinum
Ostreogricina
Ostreogrycin
Ostreogrycine
Ostreogrycinum
Patricin
Pristinamicina
Pristinamycin
Pristinamycine
Pristinamycinum
Pyostacine
RP7293
SKF 7988
Stafac
Stafac 500
Staphylomycin
Stapyocine
Streptogramin
Vernamycin
Virgimycin
Virginiamicina
Virginiamycin
Virginiamycina
Virginiamycine
Virginiamycinum
ATC D06AX10
J01FG01
CID 122731
CAS 011006761
SMILES C[C@@H]1OC(=O)[C@H](NC(=O)[C@H]2CC(=O)CCN2C(=O)[C@H](CC3=CC=C(C=C3)N(C)C)N(C)C(=O)[C@H]4CCCN4C(=O)[C@H](C)NC(=O)[C@@H]1NC(=O)C5=C(O)C=CC=N5)C6=CC=CC=C6
Formula C43H49N7O10
Molweight 823.89
Atoms 60
LogP 2.0662
Rotatable Bonds 7
H-Bond Donors 0
H-Bond Acceptors 14
CYP interactions
NameRelationsReferences
3A4Inhibitor Inducer 11130220
10651391
8849485
11996015
Transporter
AC-No.NameReferences
Q92887Canalicular multispecific organic anion transporter 116757538
Rifaximin

Java required.


Information Structure
Name Rifaximin
Synonyms
(2S,16Z,18E,20S,21S,22R,23R,24R,25S,26S,27S,28E)-5,6,21,23,25 Pentahydroxy-27-methoxy-2,4,11,16,20,22,24,26-octamethyl-2,7-(epoxypentadeca(1,11,13)tri
4-Deoxy-4-methylpyrido(1,2-1,2)imidazo(5,4-c)rifamycin SV
BRN 3584528
Fatroximin
L 105
L 105 (Ansamacrolide Antibiotic)
L 105SV
Normix
Rifacol
Rifamixin
Rifamycin L 105
Rifamycin L 105SV
Rifaxidin
Rifaximin
Rifaximina
Rifaximine
Rifaximinum
Ritacol
ATC A07AA11
D06AX11
CID 6436173
CAS 080621814
Drugbank ID DB01220
TTD Drug ID DAP001006
SMILES CO[C@H]1C=CO[C@@]2(C)OC3=C(C2=O)C4=C(C(O)=C3C)C(O)=C(NC(=O)C(C)=CC=C[C@H](C)[C@H](O)[C@@H](C)[C@@H](O)[C@@H](C)[C@H](OC(C)=O)[C@@H]1C)C5=C4N=C6C=C(C)C=CN56
Formula C43H51N3O11
Molweight 785.879
Atoms 57
LogP 6.2958
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 13
CYP interactions
NameRelationsReferences
3A4Inducer 17284510
Transporter
AC-No.NameReferences
Q92887Canalicular multispecific organic anion transporter 116757538
Amikacin

Java required.


Information Structure
Name Amikacin
Synonyms
1-N-(L(-)-gamma-Amino-alpha-hydroxybutyryl)kanamycin A
Amicacin
Amiglyde-V
Amikacin
Amikacina
Amikacine
Amikacinum
Amikavet
Antibiotic BB-K 8
BB-K 8
EINECS 253-538-5
HSDB 3583
Kaminax
Lukadin
Mikavir
O-3-Amino-3-deoxy-alpha-D-glucopyranosyl-(1-4)-O-(6-amino-6-deoxy-alpha-D-glucopyranosyl-(1-6))-N(sup 3)-(4-amino-L-2-hydroxybutyryl)-2-deoxy-L-strept
Pierami
ATC D06AX12
J01GB06
S01AA21
CID 2142
CAS 037517285
SMILES NCC[C@H](O)C(=O)N[C@@H]1C[C@H](N)[C@@H](O[C@H]2O[C@H](CN)[C@@H](O)[C@H](O)[C@H]2O)[C@H](O)[C@H]1O[C@H]3O[C@H](CO)[C@@H](O)[C@H](N)[C@H]3O
Formula C22H43N5O13
Molweight 585.603
Atoms 40
LogP -4.7827
Rotatable Bonds 10
H-Bond Donors 0
H-Bond Acceptors 18
Transporter
AC-No.NameReferences
Q92887Canalicular multispecific organic anion transporter 116757538
Extrarenal fraction 0.02
Elimination half-life 2.3h
Framycetin

Java required.


Information Structure
Name Framycetin
Synonyms
4-18-00-07476 (Beilstein Handbook Reference)
Actilin
Actiline
Antibiotique
BRN 0101621
EINECS 204-292-2
Enterfram
Framicetina
Framycetin
Framycetine
Framycetinum
Framygen
Neomycin B
Soframycin
Soframycine
ATC D06AX13
D09AA01
R01AX08
S01AA07
CID 8378
CAS 000119040
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
Transporter
AC-No.NameReferences
Q92887Canalicular multispecific organic anion transporter 116757538