Compound - Results

Demeclocycline

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Information Structure
Name Demeclocycline
Synonyms
6-Demethyl-7-chlorotetracycline
6-Demethyl-7-chlortetracycline
6-Demethylchlorotetracycline
6-Demethylchlortetracycline
6-Demetil-7-clorotetraciclina
7-Chloro-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,6,10,12,12a-pentahydroxy-1,11-dioxo-2-naphthacenecarboxamide
7-Chloro-6-demethyltetracycline
Bioterciclin
Chlortetracycline, 6-demethyl-
Clortetrin
Deganol
Demeclociclina
Demeclocycline
Demeclocyclinum
Demeclor
Demethylchlorotetracycline
Demethylchlortetracyclin
Demethylchlortetracycline
Demethylchlortetracycline Base
Demethylchlortetracyclinum
Demetraclin
Diuciclin
DMCT
DMCT (antibiotic)
EINECS 204-834-8
Elkamicina
HSDB 3051
Ledermycin
Mexocine
Novotriclina
Perciclina
RP 10192
Sumaclina
Tetracycline, 7-chloro-6-demethyl-
Tri-demethylchlortetracycline
ATC D06AA01
J01AA01
CID 5311063
CAS 000127333
TTD Drug ID DAP000402
SMILES CN(C)[C@H]1[C@@H]2C[C@@H]3[C@H](O)C4=C(Cl)C=CC(O)=C4C(=O)C3=C(O)[C@]2(O)C(=O)C(C(N)=O)=C1O
Formula C21H21ClN2O8
Molweight 464.853
Atoms 36
LogP 0.8086
Rotatable Bonds 1
H-Bond Donors 0
H-Bond Acceptors 10
Extrarenal fraction 0.6
Elimination half-life 14h
Chlortetracycline

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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
Extrarenal fraction 0.8
Elimination half-life 6h
Oxytetracycline

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Information Structure
Name Oxytetracycline
Synonyms
2-Naphthacenecarboxamide, 4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,6,10,12,12a-hexahydroxy-6-methyl-1,11-dioxo-
4-14-00-02633 (Beilstein Handbook Reference)
5-Hydroxytetracycline
Adamycin
Antibiotic TM 25
Berkmycen
Biostat
Biostat PA
BRN 2714587
Dabicycline
EINECS 201-212-8
Fanterrin
Geomycin
Geomycin (Streptomyces Vimosus)
Geotilin
HSDB 3145
Imperacin
LA 200
Lenocycline
Liquamycin
Liquamycin LA 200
Macocyn
Mycoshield TMQTHC 20
NCI-C56473
NSC-9169
Oksisyklin
Ossitetraciclina
OTC
OTC (antibiotic)
Oxitetraciclina
Oxitetracyclin
Oxitetracyclinum
Oxy-kesso-tetra
Oxymycin
Oxymykoin
Oxypam
Oxysteclin
Oxyterracin
Oxyterracine
Oxyterracyne
Oxytetracyclin
Oxytetracycline
Oxytetracycline Amphoteric
Oxytetracycline Anhydrous
Oxytetracyclinum
Pennox 200
Proteroxyna
Riomitsin
Ryomycin
Solkaciclina
Stevacin
Tarocyn
Tarosin
Teravit
Terrafungine
Terramitsin
Terramycin
Terramycin Im
Terramycin Q50
Tetrachel
Tetracycline, 5-hydroxy-
Tetran
Ursocyclin
Ursocycline
Vendarcin
ATC D06AA03
G01AA07
J01AA06
S01AA04
CID 5280972
CAS 000079572
Drugbank ID DB00759
TTD Drug ID DAP000401
SMILES CN(C)[C@H]1[C@@H]2[C@@H](O)[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 C22H24N2O9
Molweight 460.434
Atoms 37
LogP -0.6999
Rotatable Bonds 1
H-Bond Donors 0
H-Bond Acceptors 11
Extrarenal fraction 0.2
Elimination half-life 9h
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 umm
9399990
9384469
9384469
Phase2 interactions
NameReferences
GST 11807801
Transporter
AC-No.NameReferences
Q86UG4Solute carrier family 21 member 1911807801
Extrarenal fraction 0.12
Elimination half-life 6h
Meclocyclin

Java required.


Information Structure
Name Meclocyclin
Synonyms
7-Chloro-4-(dimethylamino)-1,4,4a,5,5a,6,11,12a-octahydro-3,5,10,12,12a-pentahydroxy-6-methylene-1,11-dioxo-2-naphthacenecarboxamide
7-Chloro-6-methylene-5-oxytetracycline
7-Cloro-6-metilene-5-ossitetraciclina
EINECS 217-938-3
GS 2989
Meclociclina
Meclocyclin
Meclocycline
Meclocyclinum
NSC 78502
ATC D06AA05
D10AF04
CID 54676539
CAS 002013583
SMILES CN(C)[C@H]1[C@@H]2[C@@H](O)[C@@H]3C(=C)C4=C(Cl)C=CC(O)=C4C(=O)C3=C(O)[C@]2(O)C(=O)C(C(N)=O)=C1O
Transporter
AC-No.NameReferences
Q86UG4Solute carrier family 21 member 1911807801