Compound - Results

Sulfaisodimidine

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Information Structure
Name Sulfaisodimidine
Synonyms
(p-Aminobenzolsulfonyl)-4-amino-2,6-dimethylpyrimidin
2,4-Dimethyl-6-sulfanilamidopyrimidine
2,6-Dimethyl-4-sulfanilamidopyrimidine
4-Sulfa-2,6-dimethylpyrimidine
4-Sulfanilamido-2,6-dimethylpyrimidine
5-25-10-00216 (Beilstein Handbook Reference)
6-(4-Aminobenzenesulfonamido)-2,4-dimethylpyrimidine
6-(p-Aminobenzenesulfonamido)-2,4-dimethylpyrimidine
6-(p-Aminobenzenesulfonyl)amino-2,4-dimethylpyrimidine
6-Sulfanilamido-2,4-dimethylpyrimidine
AI3-50168
Aristamid
Aristogyn
BRN 0261305
Domian
EINECS 208-204-3
Elcosine
Elkosil
Elkosin
Elkosine
Erycon
Mefenal
N(sup 1)-(2,6-Dimethyl-4-pyrimidinyl)sulfanilamide
Solfisomidina
Sulfadimetine
Sulfaisodimerazine
Sulfaisodimidine
Sulfaisodimidinum
Sulfaisomidine
Sulfamethin
Sulfasomidine
Sulfisomidin
Sulfisomidina
Sulfisomidine
Sulfisomidinum
Sulphasomidine
ATC J01EB01
CID 5343
CAS 000515640
SMILES CC1=NC(C)=NC(NS(=O)(=O)C2=CC=C(N)C=C2)=C1
Formula C12H14N4O2S
Molweight 278.33
Atoms 19
LogP 3.2114
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 6
Sulfamethizole

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Information Structure
Name Sulfamethizole
Synonyms
2-(p-Aminobenzenesulfonamido)-5-methylthiadiazole
2-Methyl-5-sulfanilamido-1,3,4-thiadiazole
2-Sulfanilamido-5-methyl-1,3,4-thiadiazole
4-Amino-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide
5-Methyl-2-sulfanilamido-1,3,4-thiadiazole
AI3-50149
Ayerlucil
Benzenesulfonamide, 4-amino-N-(5-methyl-1,3,4-thiadiazol-2-yl)-
CCRIS 756
EINECS 205-641-1
Famet
HSDB 4379
Lucosil
Methazol
Microsul
N(sup 1)-(5-Methyl-1,3,4-thiadiazol-2-yl)-sulfanilamide
N1-(5-Methyl-1,3,4-thiadiazol-2-yl)sulfanilamide
Renasul
RP 2145
Rufol
Salimol
Solfametizolo
Sulfa Gram
Sulfamethizol
Sulfamethizole
Sulfamethizolum
Sulfamethylthiadiazole
Sulfametizol
Sulfapyelon
Sulfstat
Sulfurine
Sulphamethizole
Tetracid
Thidicur
Thiosulfil
Thiosulfil Forte
Ultrasul
Urocydal
Urodiaton
Urolucosil
Urosulfin
Uroz
VK 53
ATC B05CA04
D06BA04
J01EB02
S01AB01
CID 5328
CAS 000144821
Drugbank ID DB00576
TTD Drug ID DAP001202
SMILES CC1=NN=C(NS(=O)(=O)C2=CC=C(N)C=C2)S1
Formula C9H10N4O2S2
Molweight 270.331
Atoms 17
LogP 2.9645
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 6
CYP interactions
NameRelationsReferences
2C9Inhibitor 10725317
10725317
Sulfadimidine

Java required.


Information Structure
Name Sulfadimidine
Synonyms
(p-Aminobenzolsulfonyl)-2-amino-4,6-dimethylpyrimidin
2-(p-Aminobenzenesulfonamido)-4,6-dimethylpyrimidine
2-Sulfanilamido-4,6-dimethylpyrimidine
4,6-Dimethyl-2-sulfanilamidopyrimidine
4-Amino-N-(2,6-dimethyl-4-pyrimidinyl)benzenesulfonamide
5-25-10-00250 (Beilstein Handbook Reference)
6-(4-Aminobenzol-sulfonamido)-2,4-dimethylpyrimidin
A-502
AI3-26817
Azolmetazin
Benzenesulfonamide, 4-amino-N-(2,6-dimethyl-4-pyrimidinyl)-
Benzenesulfonamide, 4-amino-N-(4,6-dimethyl-2-pyrimidinyl)-
BN 2409
BRN 0261304
Calfspan Tablets
CCRIS 3701
Cremomethazine
Diazil
Diazil (the Sulfanilamide)
Diazyl
Diazyl (VAN)
Dimezathine
Dimidin-R
EINECS 200-346-4
Hava-Span
HSDB 4157
Intradine
Kelametazine
Mermeth
Metazin
N(1)-(4,6-Dimethyl-2-pyrimidinyl)sulfanilamide
N(1)-(4,6-Dimethyl-2-pyrimidyl)sulfanilamide
N(sup 1)-(4,6-Dimethyl-2-pyrimidinyl)sulfanilamide
N(sup 1)-(4,6-Dimethyl-2-pyrimidyl)sulfanilamide
N-(4,6-Dimethyl-2-pyrimidyl)sulfanilamide
NCI-C56600
Neasina
Neazina
NSC 67457
Pirmazin
SA III
Solfadimidina
Spanbolet
Sulfa-Isodimerazine
Sulfadimerazine
Sulfadimesin
Sulfadimesine
Sulfadimethyldiazine
Sulfadimethylpyrimidine
Sulfadimezin
Sulfadimezine
Sulfadimezinum
Sulfadimidin
Sulfadimidina
Sulfadimidine
Sulfadimidinum
Sulfadine
Sulfametazina
Sulfametazyny
Sulfamethazine
Sulfamethiazine
Sulfamezathine
Sulfanilamide, N(1)-(4,6-dimethyl-2-pyrimidinyl)-
Sulfanilamide, N(sup1)-(2,6-dimethyl-4-pyrimidinyl)-
Sulfanilamide, N(sup1)-(4,6-dimethyl-2-pyrimidinyl)-
SulfaSURE SR Bolus
Sulfodimesin
Sulfodimezine
Sulka S Boluses
Sulphadimethylpyrimidine
Sulphadimidine
Sulphamethasine
Sulphamethazine
Sulphamezathine
Sulphamidine
Sulphodimezine
Superseptil
Superseptyl
Vertolan
ATC J01EB03
CID 5327
CAS 000057681
Drugbank ID DB01582
TTD Drug ID DAP001241
SMILES CC1=CC(C)=NC(NS(=O)(=O)C2=CC=C(N)C=C2)=N1
Formula C12H14N4O2S
Molweight 278.33
Atoms 19
LogP 3.2114
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 6
CYP interactions
NameRelationsReferences
2C9Inhibitor 9293615
9293615
3A4Inducer 11996015
Transporter
AC-No.NameReferences
Q99624Sodium-coupled neutral amino acid transporter 316507510
Sulfapyridine

Java required.


Information Structure
Name Sulfapyridine
Synonyms
2-(p-Aminobenzenesulphonamido)pyridine
2-Sulfanilamidopyridin
2-Sulfanilamidopyridine
2-Sulfanilyl Aminopyridine
2-Sulfanilylaminopyridine
2-Sulfapyridine
A-499
Adiplon
AI3-01049
Coccoclase
Dagenan
EINECS 205-642-7
Eubasin
Eubasinum
Haptocil
M + B 693
M&B 693
M+B 693
N(sup 1)-2-Pyridylsulfanilamide
N1-2-Pyridylsulfanilamide
NSC 41791
Piridazol
Plurazol
Pyriamid
Pyridazol
Relbapiridina
Ronin
Septipulmon
Solfapiridina
Streptosilpyridine
Sulfanilamide, N(sup 1)-2-pyridyl-
Sulfapiridina
Sulfapyridine
Sulfapyridinum
Sulfidin
Sulfidine
Sulphapyridine
Thioseptal
Trianon
ATC J01EB04
CID 5336
CAS 000144832
Drugbank ID DB00891
TTD Drug ID DAP001200
SMILES NC1=CC=C(C=C1)S(=O)(=O)NC2=CC=CC=N2
Formula C11H11N3O2S
Molweight 249.289
Atoms 17
LogP 3.1996
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 5
CYP interactions
NameRelationsReferences
2C9Inhibitor 10725317
10725317
Phase2 interactions
NameReferences
NAT 12795783,
12135032,
10030449,
12186410,
11642327,
19560446
Transporter
AC-No.NameReferences
Q99624Sodium-coupled neutral amino acid transporter 316507510
Sulfafurazole

Java required.


Information Structure
Name Sulfafurazole
Synonyms
3,4-Dimethyl-5-sulfanilamidoisoxazole
3,4-Dimethyl-5-sulfonamidoisoxazole
3,4-Dimethyl-5-sulphanilamidoisoxazole
3,4-Dimethyl-5-sulphonamidoisoxazole
3,4-Dimethylisoxazole-5-sulfanilamide
3,4-Dimethylisoxazole-5-sulphanilamide
4-27-00-04747 (Beilstein Handbook Reference)
4-Amino-N-(3,4-dimethyl-5-isoxazolyl)benzenesulphonamide
5-(4-Aminophenylsulfonamido)-3,4-dimethylisoxazole
5-(p-Aminobenzenesulfonamido)-3,4-dimethylisoxazole
5-(p-Aminobenzenesulphonamido)-3,4-dimethylisoxazole
5-Sulfanilamido-3,4-dimethylisoxazole
5-Sulphanilamido-3,4-dimethyl-isoxazole
Accuzole
AI3-24003
Alphazole
Amidoxal
Azo Gantrisin
Benzenesulfonamide, 4-amino-N-(3,4-dimethyl-5-isoxazolyl)-
BRN 0263871
CCRIS 568
Chemouag
Cosoxazole
Dorsulfan
Dorsulfan Warthausen
EINECS 204-858-9
Entusil
Entusul
Gantrisin
Gantrisine
Gantrisona
Gantrosan
HSDB 797
Isoxamin
J-Sul
Koro-sulf
N(sup 1)-(3,4-Dimethyl-5-isoxazolyl)sulfanilamide
N(sup 1)-(3,4-Dimethyl-5-isoxazolyl)sulphanilamide
N(sup1)-(3,4-Dimethyl-5-isoxazolyl)sulfanilamide
N-(3,4)Dimethylisoxazol-5-yl-sulphanilamide
N1-(3,4-Dimethyl-5-isoxazolyl)sulfanilamide
NCI-C50022
Neazolin
Neoxazol
Norilgan-S
Novazolo
Novosaxazole
NSC 13120
NU 445
Pancid
Renosulfan
Roxosul
Roxosul Tablets
Saxosozine
sk-Soxazole
Sodizole
Solfafurazolo
Sosol
Soxamide
Soxisol
Soxitabs
Soxo
Soxomide
Stansin
Sulbio
Sulfadimethylisoxazole
Sulfafurazol
Sulfafurazole
Sulfafurazolum
Sulfagan
Sulfaisoxazole
Sulfalar
Sulfapolar
Sulfasol
Sulfazin
Sulfazin (VAN)
Sulfisin
Sulfisoxasole
Sulfisoxazol
Sulfisoxazole
Sulfisoxazole Dialamine
Sulfisoxazolum
Sulfizin
Sulfizol
Sulfizole
Sulfofurazole
Sulfoxol
Sulphadimethylisoxazole
Sulphafurazole
Sulphafurazolum
Sulphaisoxazole
Sulsoxin
Thiasin
TL-Azole
U.S.-67
Unisulf
Urisoxin
Uritrisin
Urogan
V-Sul
Vagilia
ATC J01EB05
S01AB02
CID 5344
CAS 000127695
Drugbank ID DB00263
TTD Drug ID DAP001203
SMILES CC1=NOC(NS(=O)(=O)C2=CC=C(N)C=C2)=C1C
Formula C11H13N3O3S
Molweight 267.304
Atoms 18
LogP 3.4094
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 6
CYP interactions
NameRelationsReferences
2C8Substrate Inhibitor umm
2C9Substrate Inhibitor umm
10725317
Transporter
AC-No.NameReferences
Q99624Sodium-coupled neutral amino acid transporter 316507510
Extrarenal fraction 0.5
Elimination half-life 8h
Sulfanilamide

Java required.


Information Structure
Name Sulfanilamide
Synonyms
1162 F
4-14-00-02658 (Beilstein Handbook Reference)
4-Aminobenzenesulfonamide
4-Aminophenylsulfonamide
4-Sulfamoylaniline
A-349
AI3-00952
Albexan
Albosal
Ambeside
Aniline-p-sulfonic Amide
Antistrept
Astreptine
Astrocid
Bacteramid
Bactesid
Benzenesulfonamide, 4-amino-
Benzenesulfonamide, P-amino-
BRN 0511852
Caswell No. 809A
CCRIS 764
Collomide
Colsulanyde
Copticide
Deseptyl
Dipron
EINECS 200-563-4
EPA Pesticide Chemical Code 077902
Ergaseptine
Erysipan
Estreptocida
Exoseptoplix
F 1162
F-1162
Fourneau 1162
Gerison
Gombardol
HSDB 223
Infepan
Lusil
Lysococcine
Neococcyl
NSC 7618
Orgaseptine
p-Aminobenzenesulfamide
p-Aminobenzenesulfonamide
p-Aminobenzenesulfonylamide
p-Aminophenylsulfonamide
p-Anilinesulfonamide
p-Sulfamidoaniline
p-Sulfamoylaniline
PABS
Prontalbin
Prontosil Album
Prontosil I
Prontosil White
Prontylin
Pronzin Album
Proseptal
Proseptine
Proseptol
Pysococcine
Rubiazol A
Sanamid
Septamide Album
Septanilam
Septinal
Septolix
Septoplex
Septoplix
Solfanilamide
Stopton Album
Stramid
Strepamide
Strepsan
Streptagol
Streptamid
Streptamin
Streptasol
Streptocid
Streptocid Album
Streptocide (VAN)
Streptocide White
Streptocidum
Streptoclase
Streptocom
Streptol
Strepton
Streptopan
Streptosil
Streptozol
Streptozone
Streptrocide
Sulfamidyl
Sulfamine
Sulfana
Sulfanalone
Sulfanidyl
Sulfanil
Sulfanilamida
Sulfanilamide
Sulfanilamide Vaginal Cream
Sulfanilamidum
Sulfanilimidic Acid
Sulfocidin
Sulfocidine
Sulfonamide
Sulfonamide P
Sulfonylamide
Sulphanilamide
Sulphonamide
Therapol
Tolder
White Streptocide
ATC J01EB06
D06BA05
CID 5333
CAS 000063741
Drugbank ID DB00259
TTD Drug ID DAP001193
SMILES NC1=CC=C(C=C1)S(N)(=O)=O
Formula C6H8N2O2S
Molweight 172.205
Atoms 11
LogP 2.2785
Rotatable Bonds 1
H-Bond Donors 0
H-Bond Acceptors 4
CYP interactions
NameRelationsReferences
2C9Inhibitor 14739663
2C19Inhibitor 14739663
2D6Inhibitor 14739663
2E1Inhibitor 14739663
3A4Inhibitor 14739663
Transporter
AC-No.NameReferences
Q99624Sodium-coupled neutral amino acid transporter 316507510
Sulfathiazole

Java required.


Information Structure
Name Sulfathiazole
Synonyms
2-(p-Aminobenzenesulfonamido)thiazole
2-(p-Aminobenzenesulphonamido)thiazole
2-(Sulfanilylamino)thiazole
2-Sulfanilamidothiazol
2-Sulfanilamidothiazole
2-Sulfonamidothiazole
2090 R.P.
2090 Rp
4-Amino-N-2-thiazolylbenzenesulfonamide
AI3-01050
Azoquimiol
Azoseptale
Benzenesulfonamide, 4-amino-N-2-thiazolyl-
Caswell No. 809B
CCRIS 765
Cerazol (suspension)
Cerazole
Chemosept
Ciba 3714
Cibazol
Coco-Thiazole
Duatok
Dulana
EINECS 200-771-5
Eleudron
EPA Pesticide Chemical Code 077903
Estafilol
Formosulfathiazole
HSDB 4380
M&B 760
M+B 760
N(1)-2-Thiazolylsulfanilamide
N(sup 1)-2-Thiazolylsulfanilamide
Neostrepsan
Norsulfasol
Norsulfazol
Norsulfazole
Norsulfazolum
NSC 31812
Planomide
Poliseptil
RP 2090
Sanotiazol
Septozol
Solfatiazolo
Streptosilthiazole
Sulfamul
Sulfanilamide, N(1)-2-thiazolyl-
Sulfanilamide, N(sup 1)-2-thiazolyl-
Sulfanilamidothiazole
Sulfathiazol
Sulfathiazole
Sulfathiazolum
Sulfatiazol
Sulfocerol
Sulphathiazole
Sulzol
Thiacoccine
Thiasulfol
Thiazamide
Thiozamide
USAF SN-9
Wintrazole
ATC J01EB07
D06BA02
CID 5340
CAS 000072140
SMILES NC1=CC=C(C=C1)S(=O)(=O)NC2=NC=CS2
Formula C9H9N3O2S2
Molweight 255.317
Atoms 16
LogP 3.2611
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 5
Transporter
AC-No.NameReferences
Q99624Sodium-coupled neutral amino acid transporter 316507510
Sulfathiourea

Java required.


Information Structure
Name Sulfathiourea
Synonyms
2-Sulfanilamidothiokarbamid
4-14-00-02671 (Beilstein Handbook Reference)
4-Amino-N-(aminothioxomethyl)benzenesulfonamide
Badional
Baldinol
BRN 2696478
EINECS 208-201-7
Fontamide
NSC 108228
p-Aminobenzenesulfonylthiourea
p-Aminophenylsulfonylthiourea
R.P. 2255
RP 2255
Salvoseptyl
Solfatiourea
Solufontamide
Sulfanilamide, N(sup1)-(thiocarbamoyl)-
Sulfanilthiocarbamide
Sulfanilthiourea
Sulfathiocarbamid
Sulfathiocarbamide
Sulfathiocarbamidum
Sulfathiourea
Sulfathiouree
Sulfatiourea
Sulphathiourea
ATC J01EB08
CID 3000579
CAS 000515491
SMILES NC(=S)NS(=O)(=O)C1=CC=C(N)C=C1
Formula C7H9N3O2S2
Molweight 231.295
Atoms 14
LogP 2.5439
Rotatable Bonds 3
H-Bond Donors 0
H-Bond Acceptors 5
Transporter
AC-No.NameReferences
Q99624Sodium-coupled neutral amino acid transporter 316507510