Compound Summary
Compound Information
triamterene
Compound Name: | triamterene |
Compound CID: | 5546 |
Synonyms: | triamterene 396-01-0 6-phenylpteridine-2,4,7-triamine 2,4,7-Triamino-6-phenylpteridine Dyrenium More... |
Iupac Name: | 6-phenylpteridine-2,4,7-triamine |
InChI: | InChI=1S/C12H11N7/c13-9-7(6-4-2-1-3-5-6)16-8-10(14)18-12(15)19-11(8)17-9/h1-5H,(H6,13,14,15,17,18,19) |
InChIKey: | FNYLWPVRPXGIIP-UHFFFAOYSA-N |
Canonical Smiles: | C1=CC=C(C=C1)C2=NC3=C(N=C(N=C3N=C2N)N)N |
Isomeric Smiles: | C1=CC=C(C=C1)C2=NC3=C(N=C(N=C3N=C2N)N)N |
Molecular Weight: | 253.26 |
Molecular Formula: | C12H11N7 |
Compound Structure
2D Structure:
3D Structure:
Computed Properties
triamterene
Molecular Weight: | 253.26 |
Molecular Formula: | C12H11N7 |
Hydrogen Bond Donor Count: | 3 |
Hydrogen Bond Acceptor Count: | 7 |
Rotatable Bond Count: | 1 |
Heavy Atom Count: | 19 |
Complexity: | 307 |
Synonyms
triamterene
| triamterene | triamterene |
|---|---|
triamterene |
396-01-0 |
6-phenylpteridine-2,4,7-triamine |
2,4,7-Triamino-6-phenylpteridine |
Dyrenium |
Dytac |
Pterofen |
Pterophene |
Triamteren |
Triamteril |
Triteren |
Ademin |
Ademine |
Diurene |
Noridil |
Taturil |
Teridin |
Urocaudal |
Jatropur |
Noridyl |
Triampur |
Diren |
Ditak |
Dyren |
Teriam |
Tri-Span |
Triamteril complex |
Trispan |
6-Phenyl-2,4,7-pteridinetriamine |
2,4,7-Pteridinetriamine, 6-phenyl- |
SK&F 8542 |
6-Phenyl-2,4,7-triaminopteridine |
SKF 8542 |
Pteridine, 2,4,7-triamino-6-phenyl- |
2,4,7-Triamino-6-fenilpteridina |
C12H11N7 |
UNII-WS821Z52LQ |
BRN 0266723 |
Diucelpin |
NSC-77625 |
SK-8542 |
WS821Z52LQ |
Masuharmin |
Triamizide |
Triamthiazid |
Amteren |
Dinazide |
Diutensat |
Diuteren |
Dyberzide |
Dytenzide |
Esiteren |
Hidiurese |
Hydrene |
Hypertorr |
Jenateren |
Kalspare |
Nephral |
Renezide |
Reviten |
Tricilone |
Triurene |
Uretren |
Diarol |
Isobar |
Trizid |
Anjal |
Dazid |
Turfa |
Apo-triazide |
Thiazid Wolff |
NCI-C56042 |
NSC77625 |
Ademin(e) |
MFCD00006708 |
NCGC00016016-10 |
Triamterena |
Triamterenum |
CAS-396-01-0 |
Triazide |
Fluss 40 |
SALI-PUREN |
DSSTox_CID_1373 |
DSSTox_RID_76117 |
DSSTox_GSID_21373 |
Triamterenum INN-Latin |
Triamterena INN-Spanish |
Dyrenium (TN) |
CCRIS 5872 |
Pteridine deriv. 11 |
HSDB 3405 |
2,4,7-Triamino-6-fenilpteridina Italian |
NCI C56042 |
SR-01000002968 |
EINECS 206-904-3 |
NSC 77625 |
NSC 639359 |
AI3-60017 |
Prestwick_480 |
SK&F-8542 |
Dyazide (Salt/Mix) |
Triamterene USAN:USP:INN:BAN:JAN |
Spectrum_000508 |
Triamterene, >=99% |
Prestwick0_000034 |
Prestwick1_000034 |
Prestwick2_000034 |
Prestwick3_000034 |
Spectrum2_000938 |
Spectrum3_001372 |
Spectrum4_000366 |
Spectrum5_001034 |
Lopac-T-4143 |
ACMC-1CT1F |
CHEMBL585 |
T 4143 |
NCIOpen2_004741 |
Lopac0_001196 |
Oprea1_825704 |
SCHEMBL40707 |
BSPBio_000127 |
BSPBio_002924 |
KBioGR_000831 |
KBioSS_000988 |
5-26-17-00447 (Beilstein Handbook Reference) |
MLS000069431 |
ARONIS23836 |
BIDD:GT0534 |
DivK1c_000433 |
SPECTRUM1500589 |
SPBio_000876 |
SPBio_002048 |
BDBM6644 |
BPBio1_000141 |
CHEBI:9671 |
GTPL4329 |
Triamterene (JP17/USP/INN) |
2,7-Triamino-6-phenylpteridine |
6-Phenyl-2,7-triaminopteridine |
DTXSID6021373 |
HMS501F15 |
KBio1_000433 |
KBio2_000988 |
KBio2_003556 |
KBio2_006124 |
KBio3_002144 |
SKF8542 |
NINDS_000433 |
3-Bromobiphenyl-3-carboxylicacid |
HMS1568G09 |
HMS2092O17 |
HMS2095G09 |
HMS2232B04 |
HMS3259C08 |
HMS3263P13 |
HMS3371D10 |
HMS3652E10 |
HMS3712G09 |
Pharmakon1600-01500589 |
ZINC120286 |
2,7-Pteridinetriamine, 6-phenyl- |
Pteridine,4,7-triamino-6-phenyl- |
BCP28855 |
EBD44439 |
HY-B0575 |
2,4,7-triamino-6-phenyl-pteridine |
Tox21_110283 |
Tox21_202021 |
Tox21_302833 |
Tox21_501196 |
BBL023360 |
CCG-40090 |
NSC639359 |
NSC757367 |
s4080 |
SBB017574 |
STK300348 |
AKOS003790819 |
Tox21_110283_1 |
DB00384 |
LP01196 |
MCULE-5832721534 |
NC00544 |
NSC-639359 |
NSC-757367 |
SDCCGSBI-0051163.P004 |
IDI1_000433 |
SMP1_000147 |
NCGC00016016-01 |
NCGC00016016-02 |
NCGC00016016-03 |
NCGC00016016-04 |
NCGC00016016-05 |
NCGC00016016-06 |
NCGC00016016-07 |
NCGC00016016-08 |
NCGC00016016-09 |
NCGC00016016-11 |
NCGC00016016-12 |
NCGC00016016-13 |
NCGC00016016-14 |
NCGC00016016-15 |
NCGC00016016-16 |
NCGC00016016-18 |
NCGC00016016-28 |
NCGC00016016-29 |
NCGC00023458-03 |
NCGC00023458-04 |
NCGC00023458-05 |
NCGC00023458-06 |
NCGC00023458-07 |
NCGC00256495-01 |
NCGC00259570-01 |
NCGC00261881-01 |
AC-14066 |
AS-12471 |
SMR000059118 |
ST093702 |
SBI-0051163.P003 |
AB0011988 |
DB-049442 |
AB00052116 |
B2275 |
BB 0256885 |
EU-0101196 |
SW196688-3 |
T1288 |
Triamterene 1.0 mg/ml in Dimethyl Sulfoxide |
Dyrenium|||2,4,7-Triamino-6-phenylpteridine |
D00386 |
D95706 |
WLN: T66 BN DN GN JNJ CZ EZ HR& IZ |
AB00052116_13 |
AB00052116_14 |
396T010 |
A824641 |
Q221520 |
SR-01000002968-2 |
SR-01000002968-4 |
SR-01000002968-6 |
BRD-K92049597-001-05-9 |
BRD-K92049597-001-10-9 |
Z275128596 |
Triamterene, British Pharmacopoeia (BP) Reference Standard |
Triamterene, European Pharmacopoeia (EP) Reference Standard |
Triamterene, United States Pharmacopeia (USP) Reference Standard |
Triamterene, Pharmaceutical Secondary Standard; Certified Reference Material |
Experimental Data
triamterene
| Species | Dosage | Unit | CG Lifespan(AVG/MED days) | TG Lifespan(AVG/MED days) | Lifespan Change(AVG/MED%) | CG Lifespan(MAX days) | TG Lifespan(MAX days) | Lifespan Change(MAX%) | Significant | Strain | Gender | PubMed | Active Label |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Caenorhabditis elegans | 33 | umol/L | -2 | NS | N2 | 24134630 | Inactive |
Experimental Data Visualization
triamterene
Statistics Data
triamterene
| Species | Lifespan Change(AVG/MED%) | Lifespan Change(MAX%) | Count Reference | Count Data point |
|---|---|---|---|---|
| Caenorhabditis elegans | -2 | 1 | 1 |
Statistics Data Visualization
triamterene
