Interesting facts
Interesting Facts about 6-Phenylpteridine-2,4,7-triamine
6-Phenylpteridine-2,4,7-triamine, a fascinating compound in the realm of medicinal chemistry, belongs to a class of organic compounds known for their diverse applications. This particular compound can be characterized by the following features:
- Structural Diversity: The presence of the pteridine ring system combined with a phenyl group allows for a *unique molecular architecture* that can influence the compound's biological activity.
- Biological Significance: Compounds like 6-phenylpteridine-2,4,7-triamine have been studied for their potential role in treating various diseases, making them a vital interest in pharmaceutical research.
- Interdisciplinary Connections: This compound sits at the intersection of *organic chemistry, biochemistry,* and *pharmacology,* highlighting how different scientific disciplines can work together towards common goals in health and medicine.
- Synthetic Routes: The synthesis of this compound offers chemists the opportunity to explore various *reaction mechanisms* and *synthetic pathways*, furthering their understanding of complex organic synthesis.
As noted in the literature, “the potential for newly synthesized molecules to exhibit novel therapeutic properties is a captivating area of research.” Such compounds often serve as templates for the development of new drugs, inspiring chemists to innovate further.
In summary, 6-phenylpteridine-2,4,7-triamine is not just a compound of chemical interest; it symbolizes the *interplay between structure and function* in chemical biology. Its study can lead to breakthroughs in treatments for various ailments, showcasing the critical role of chemistry in healthcare.
Synonyms
triamterene
396-01-0
6-phenylpteridine-2,4,7-triamine
2,4,7-Triamino-6-phenylpteridine
Dyrenium
Diurene
Noridil
Pterofen
Pterophene
Taturil
Teridin
Triamteren
Triamteril
Triteren
Ademin
Dytac
Jatropur
Triampur
Ademine
Noridyl
Teriam
Diren
Ditak
Dyren
Tri-Span
Urocaudal
Trispan
6-Phenyl-2,4,7-pteridinetriamine
Diucelpin
Masuharmin
Triamizide
Triamthiazid
Amteren
Dinazide
Diutensat
Diuteren
Dyberzide
Dytenzide
Esiteren
Hidiurese
Hypertorr
Jenateren
Kalspare
Nephral
Renezide
Reviten
Tricilone
Triurene
Uretren
Anjal
Dazid
Diarol
Isobar
Trizid
Turfa
Apo-triazide
Thiazid Wolff
2,4,7-Pteridinetriamine, 6-phenyl-
Ademin(e)
SK&F 8542
Triamterenum
Triamterena
Fluss 40
SALI-PUREN
6-Phenyl-2,4,7-triaminopteridine
SKF 8542
Pteridine, 2,4,7-triamino-6-phenyl-
Triamterenum [INN-Latin]
Triamterena [INN-Spanish]
2,4,7-Triamino-6-fenilpteridina
NSC 77625
NSC-77625
Triamtereno
CCRIS 5872
SK-8542
BRN 0266723
HSDB 3405
NCI C56042
EINECS 206-904-3
UNII-WS821Z52LQ
SK&F-8542
NSC 639359
WS821Z52LQ
DTXSID6021373
AI3-60017
Triamterene (Standard)
NCI-C56042
NSC77625
MFCD00006708
NSC-639359
CHEBI:9671
DTXCID001373
Hydrene
5-26-17-00447 (Beilstein Handbook Reference)
DYAZIDE COMPONENT TRIAMTERENE
MAXZIDE COMPONENT TRIAMTERENE
NSC639359
Triamterene [USAN:USP:INN:BAN:JAN]
NCGC00016016-10
CAS-396-01-0
Triazide
TRIAMTERENE (IARC)
TRIAMTERENE [IARC]
Triamterenum (INN-Latin)
Triamterena (INN-Spanish)
TRIAMTERENE (MART.)
TRIAMTERENE [MART.]
TRIAMTERENE (USP-RS)
TRIAMTERENE [USP-RS]
TRIAMTERENE (EP MONOGRAPH)
TRIAMTERENE (USP IMPURITY)
TRIAMTERENE [EP MONOGRAPH]
TRIAMTERENE [USP IMPURITY]
TRIAMTERENE (USP MONOGRAPH)
TRIAMTERENE [USP MONOGRAPH]
Triamterene (USAN:USP:INN:BAN:JAN)
Dyrenium (TN)
Pteridine deriv. 11
2,4,7-Triamino-6-fenilpteridina [Italian]
SR-01000002968
Triamterene?
Prestwick_480
Triamterene Capsules
Dyazide (Salt/Mix)
Triamterenum (Latin)
Spectrum_000508
Triamterene, >=99%
TRIAMTERENE [MI]
Prestwick0_000034
Prestwick1_000034
Prestwick2_000034
Prestwick3_000034
Spectrum2_000938
Spectrum3_001372
Spectrum4_000366
Spectrum5_001034
Lopac-T-4143
TRIAMTERENE [INN]
TRIAMTERENE [JAN]
TRIAMTERENE [HSDB]
TRIAMTERENE [USAN]
CHEMBL585
T 4143
TRIAMTERENE [VANDF]
NCIOpen2_004741
Lopac0_001196
Oprea1_825704
SCHEMBL40707
BSPBio_000127
BSPBio_002924
KBioGR_000831
KBioSS_000988
TRIAMTERENE [WHO-DD]
MLS000069431
BIDD:GT0534
DivK1c_000433
SPECTRUM1500589
SPBio_000876
SPBio_002048
BDBM6644
BPBio1_000141
GTPL4329
Triamterene (JP18/USP/INN)
2,7-Triamino-6-phenylpteridine
6-Phenyl-2,7-triaminopteridine
HMS501F15
HY-B0575R
KBio1_000433
KBio2_000988
KBio2_003556
KBio2_006124
KBio3_002144
C03DB02
TRIAMTERENE [ORANGE BOOK]
NINDS_000433
HMS1568G09
HMS2092O17
HMS2095G09
HMS2232B04
HMS3259C08
HMS3263P13
HMS3371D10
HMS3652E10
HMS3712G09
Pharmakon1600-01500589
2,7-Pteridinetriamine, 6-phenyl-
Pteridine,4,7-triamino-6-phenyl-
BCP28855
HY-B0575
Tox21_110283
Tox21_202021
Tox21_302833
Tox21_501196
CCG-40090
NSC757367
s4080
STK300348
AKOS003790819
Tox21_110283_1
DB00384
FT28388
LP01196
NC00544
NSC-757367
SDCCGSBI-0051163.P004
TRIAMTERENE COMPONENT OF DYAZIDE
TRIAMTERENE COMPONENT OF MAXZIDE
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
SBI-0051163.P003
DB-049442
AB00052116
CS-0695001
EU-0101196
NS00010256
SW196688-3
T1288
Triamterene 1.0 mg/ml in Dimethyl Sulfoxide
D00386
D95706
EN300-119540
WLN: T66 BN DN GN JNJ CZ EZ HR& IZ
2,4-DIAMINO-6-PHENYL-7-PTERIDINYLAMINE
AB00052116_13
AB00052116_14
A824641
Q221520
SR-01000002968-2
SR-01000002968-4
SR-01000002968-6
BRD-K92049597-001-05-9
BRD-K92049597-001-10-9
BRD-K92049597-001-19-0
BRD-K92049597-001-20-8
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
206-904-3
Solubility of 6-phenylpteridine-2,4,7-triamine (C20H17N7)
The solubility of 6-phenylpteridine-2,4,7-triamine is an intriguing aspect to consider, particularly due to its unique structural characteristics. This compound exhibits moderate solubility in various solvents, influenced by its organic nature and nitrogen content. Below are some key points regarding its solubility:
In summary, understanding the solubility of 6-phenylpteridine-2,4,7-triamine can inform its practical applications, such as in pharmaceuticals or material sciences, highlighting the importance of solvent choice in experimental protocols.