Compounds > t 1982
Page last updated: 2024-12-07

t 1982

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

1,3,4,6,7,8-hexahydro-2H-pyrimido(1,2-a)pyrimidine: structure in first source [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID79873
CHEBI ID94622
SCHEMBL ID51453
MeSH IDM0109884

Synonyms (43)

Synonym
1,3,4,6,7,8-hexahydro-2h-pyrimido(1,2-a)pyrimidine
1,3,4,6,7,8-hexahydro-2h-pyrimido[1,2-a]pyrimidine
2h-pyrimido[1,2-a]pyrimidine, 1,3,4,6,7,8-hexahydro-
1,5,7-triazabicyclo[4.4.0]dec-5-ene, 98%
hhpp
FT-0690905
3,4,6,7,8,9-hexahydro-2h-pyrimido[1,2-a]pyrimidine
A831720
unii-kaf7gn82tm
2h-pyrimido(1,2-a)pyrimidine, 1,3,4,6,7,8-hexahydro-
einecs 227-367-1
kaf7gn82tm ,
5807-14-7
1,5,7-triazabicyclo[4.4.0]dec-5-ene
T1982
AKOS006222316
triazabicyclodecene
2,3,4,6,7,8-hexahydro-1h-pyrimido[1,2-a]pyrimidine
BRD-K45542213-001-01-4
CS-B0736
SCHEMBL51453
1,5,7-triazabicyclo[4.4.0]deca-5-ene
1,3,4,6,7,8,-hexahydro-2h-pyrimido(1,2-a)pyrimidine
1,5,7-triazabicyclo[4,4,0] dec-5-ene
1,5,7-triazabicyclo[4,4,0]dec-5-ene
1,5,7-triazabicyclo [4.4.0]dec-5-ene
1,5,7-triazabicyclo(4.4.0)dec-5-ene
DTXSID10206793
mfcd00043003
J-509567
1,5,7-triazabicyclo[4.4.0]dec-5-ene, purum, >=98.0% (t)
CHEBI:94622
1,5,7-triazabicylo[4.4.0]dec-5-ene
DS-15178
BCP09211
Q7840264
A930606
SY013446
PB43106
1h,2h,3h,4h,6h,7h,8h-[1,3]diazino[1,2-a]pyrimidine
EN300-267515
PD053640
HY-59156
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
pyrimidinesAny compound having a pyrimidine as part of its structure.
[compound class information is derived from Chemical Entities of Biological Interest (ChEBI), Hastings J, Owen G, Dekker A, Ennis M, Kale N, Muthukrishnan V, Turner S, Swainston N, Mendes P, Steinbeck C. (2016). ChEBI in 2016: Improved services and an expanding collection of metabolites. Nucleic Acids Res]

Research

Studies (19)

TimeframeStudies, This Drug (%)All Drugs %
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's3 (15.79)29.6817
2010's16 (84.21)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 20.70

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be moderate demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index20.70 (24.57)
Research Supply Index3.00 (2.92)
Research Growth Index4.88 (4.65)
Search Engine Demand Index13.88 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (20.70)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other19 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
pyridine
azine : An organonitrogen compound of general structure RCH=N-N=CHR or RR'C=N-N=CRR'.		2.0410azaarene;
mancude organic heteromonocyclic parent;
monocyclic heteroarene;
pyridines		environmental contaminant;
NMR chemical shift reference compound
guanidine
Guanidine: A strong organic base existing primarily as guanidium ions at physiological pH. It is found in the urine as a normal product of protein metabolism. It is also used in laboratory research as a protein denaturant. (From Martindale, the Extra Pharmacopoeia, 30th ed and Merck Index, 12th ed) It is also used in the treatment of myasthenia and as a fluorescent probe in HPLC.. guanidine : An aminocarboxamidine, the parent compound of the guanidines.		2.4920carboxamidine;
guanidines;
one-carbon compound
4-butyrolactone
4-Butyrolactone: One of the FURANS with a carbonyl thereby forming a cyclic lactone. It is an endogenous compound made from gamma-aminobutyrate and is the precursor of gamma-hydroxybutyrate. It is also used as a pharmacological agent and solvent.. tetrahydrofuranone : Any oxolane having an oxo- substituent at any position on the tetrahydrofuran ring.. gamma-butyrolactone : A butan-4-olide that is tetrahydrofuran substituted by an oxo group at position 2.		2.0710butan-4-olidemetabolite;
neurotoxin
3-hydroxybutanal
[no description available]		2.0610
melamine
melamine: RN given refers to parent cpd; structure. melamine : A trimer of cyanamide, with a 1,3,5-triazine skeleton.		2.1110triamino-1,3,5-triazinexenobiotic metabolite
dipicrylamine
dipicrylamine: RN given refers to parent cpd; structure		2.0610
beta-butyrolactone
beta-butyrolactone: structure		2.0710beta-lactone
carbonates
Carbonates: Salts or ions of the theoretical carbonic acid, containing the radical CO2(3-). Carbonates are readily decomposed by acids. The carbonates of the alkali metals are water-soluble; all others are insoluble. (From Grant & Hackh's Chemical Dictionary, 5th ed). carbonates : Organooxygen compounds that are salts or esters of carbonic acid, H2CO3.		2.1310carbon oxoanion
zirconium
Zirconium: A rather rare metallic element with atomic number 40, atomic weight 91.224, and symbol Zr.		2.1110titanium group element atom
cupric chloride
cupric chloride: RN given refers to unlabeled parent cpd. copper(II) chloride : An inorganic chloride of copper in which the metal is in the +2 oxidation state.		2.0510copper molecular entity;
inorganic chloride		EC 5.3.3.5 (cholestenol Delta-isomerase) inhibitor
phenyl acetate
phenyl acetate: The ester formed between phenol and acetic acid. Don't confuse with phenylacetic acid derivatives listed under PHENYLACETATES.. phenyl acetate : An acetate ester obtained by the formal condensation of phenol with acetic acid.		2.1310benzenes;
phenyl acetates
1,8-diazabicyclo(5.4.0)undec-7-ene
[no description available]		2.0710
proline
Proline: A non-essential amino acid that is synthesized from GLUTAMIC ACID. It is an essential component of COLLAGEN and is important for proper functioning of joints and tendons.. proline : An alpha-amino acid that is pyrrolidine bearing a carboxy substituent at position 2.		2.4620amino acid zwitterion;
glutamine family amino acid;
L-alpha-amino acid;
proline;
proteinogenic amino acid		algal metabolite;
compatible osmolytes;
Escherichia coli metabolite;
micronutrient;
mouse metabolite;
nutraceutical;
Saccharomyces cerevisiae metabolite
morpholine-2,5-dione
morpholine-2,5-dione: structure in first source		2.1710
bemp phosphazene
BEMP phosphazene: structure in first source		2.0710
ConditionIndicatedRelationship StrengthStudiesTrials