Page last updated: 2024-11-04

1,2-cyclohexanediamine

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

Description

1,2-cyclohexanediamine is a cyclic diamine with the formula C6H12(NH2)2. It is a colorless liquid that is soluble in water. 1,2-cyclohexanediamine is used as a monomer in the production of polyamides, such as nylon. It is also used as a catalyst in the synthesis of other organic compounds. 1,2-cyclohexanediamine is studied because of its potential applications in a variety of fields, including materials science, pharmaceuticals, and agriculture. 1,2-cyclohexanediamine is a versatile molecule with a wide range of potential applications. It is also a relatively inexpensive and readily available chemical. These factors make it an attractive candidate for further research and development.'

1,2-cyclohexanediamine: RN given refers to cpd without isomeric designation [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID4610
CHEMBL ID1356279
CHEBI ID93778
SCHEMBL ID687020
SCHEMBL ID29457
MeSH IDM0096264

Synonyms (72)

Synonym
EN300-19626
dach
1,2-diaminocyclohexane
(+)-s,s-1,2-diaminocyclohexane
1,2-cyclohexanediamine
694-83-7
cyclohexane-1,2-diamine
einecs 211-776-7
1,2-cylohexanediamine
cyclohex-1,2-ylenediamine
brn 0506142
hsdb 5748
trans-1,2-cyclohexaneiamine
nsc-362640
nsc362641
nsc-362641
nsc362640
NCGC00166039-01
D0277
L000760
AKOS000119859
NCGC00166039-02
dtxcid707301
tox21_303220
dtxsid0027301 ,
NCGC00257130-01
cas-694-83-7
tox21_201883
NCGC00259432-01
0-13-00-00001 (beilstein handbook reference)
c82tx76bhh ,
ec 211-776-7
unii-c82tx76bhh
FT-0606333
FT-0604536
FT-0623876
FT-0647969
FT-0604562
STL372729
AM20070551
SCHEMBL687020
BBL027344
SCHEMBL29457
cyclohexane 1,2-diamine
1,2-diamino cyclohexane
rac-(1r,2r)-cyclohexane-1,2-diamine
mfcd00062985
SY001269
dch-99
cyclohexanediamine1,2-cyclohexanediamine
1,2-diaminocyclohexane,c&t
CHEMBL1356279
AKOS016842498
W-104620
(1r,2r)-(-)-1,2-diamino cyclohexane
mfcd00001491
CHEBI:93778
BCP22662
(1r,2r)-cyclohexane-1,2-diamine;(1r,2r)-(-)-1,2-cyclohexanediamine
BCP04075
Q27165475
6-methoxypyridine-2-carboxylicacidhydrazide
VS-08529
(1r,2s)-1,2-diaminocyclohexane; (r)(s)-1,2-diaminocyclohexane; (+/-)-cis-cyclohexane-1,2-diamine; cis-(1s,2r)-1,2-diaminocyclohexane; cis-1,2-cyclohexanediamine; cis-1,2-diaminocyclohexane
pyridoxal, 5-(dihydrogen phosphate), calcium salt (1:1) (8ci)
(rel)-oxaliplatin
pyridoxal phosphate (calcium salt)
disperseorange37
SB44188
SY004140
PB47571
Z104474510

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" However, the optimal regimen regarding frequency and dosing as well as combination and maintenance therapy is not well established."( The optimal use of chlormethine gel for mycosis fungoides: An expert consensus from Germany, Austria and Switzerland (DACH region).
Assaf, C; Booken, N; Dippel, E; Guenova, E; Jonak, C; Klemke, CD; Nicolay, JP; Schlaak, M; Trautinger, F; Wobser, M, 2022
)
0.72
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Drug Classes (1)

ClassDescription
primary aliphatic amine
[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]

Protein Targets (5)

Potency Measurements

ProteinTaxonomyMeasurementAverage (µ)Min (ref.)Avg (ref.)Max (ref.)Bioassay(s)
acetylcholinesteraseHomo sapiens (human)Potency53.92960.002541.796015,848.9004AID1347395; AID1347398
AR proteinHomo sapiens (human)Potency1.24470.000221.22318,912.5098AID743036
estrogen-related nuclear receptor alphaHomo sapiens (human)Potency34.76110.001530.607315,848.9004AID1224841
peroxisome proliferator activated receptor gammaHomo sapiens (human)Potency19.49620.001019.414170.9645AID743094
thyroid hormone receptor beta isoform 2Rattus norvegicus (Norway rat)Potency0.55090.000323.4451159.6830AID743065
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (120)

TimeframeStudies, This Drug (%)All Drugs %
pre-19904 (3.33)18.7374
1990's17 (14.17)18.2507
2000's38 (31.67)29.6817
2010's46 (38.33)24.3611
2020's15 (12.50)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 30.28

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 Index30.28 (24.57)
Research Supply Index4.83 (2.92)
Research Growth Index5.16 (4.65)
Search Engine Demand Index36.91 (26.88)
Search Engine Supply Index2.00 (0.95)

This Compound (30.28)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews6 (4.84%)6.00%
Case Studies1 (0.81%)4.05%
Observational0 (0.00%)0.25%
Other117 (94.35%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]