3,4-Dihydropyran is a heterocyclic compound with a six-membered ring containing one oxygen atom and a double bond. It is a colorless liquid that is used as a reagent in organic synthesis. It is particularly important in the synthesis of pyrans, which are important building blocks for many organic molecules. 3,4-dihydropyran can be synthesized by a variety of methods, including the Diels-Alder reaction and the ring-opening metathesis polymerization. It is studied due to its potential applications in pharmaceuticals, materials science, and agrochemicals. The compound exhibits a variety of biological activities, such as antimicrobial and anti-inflammatory effects, making it a promising lead compound for drug development.'
ID Source | ID |
---|---|
PubMed CID | 8080 |
CHEMBL ID | 3184439 |
MeSH ID | M0199454 |
Synonym |
---|
dihydro-2h-pyran |
2h-pyran, dihydro- |
3,4-dihydropyran |
2,3-dihydro-4h-pyran |
.delta.2-dihydropyran |
2h-3,4-dihydropyran |
nsc-57860 |
dihydropyran |
nsc57860 |
110-87-2 |
wln: t6o butj |
5,6-dihydro-4h-pyran |
pyran, 2,3-dihydro- |
.delta.(sup2)-dihydropyran |
nsc-73472 |
nsc73472 |
inchi=1/c5h8o/c1-2-4-6-5-3-1/h2,4h,1,3,5h |
3,4-dihydro-2h-pyran |
2h-pyran, 3,4-dihydro- |
3,4-dihydro-2h-pyran, 97% |
D0555 |
2,3-dihydropyran |
AKOS000121126 |
NCGC00248323-01 |
dihydropyrane |
2,3-dihydropyrane |
NCGC00255086-01 |
cas-110-87-2 |
dtxcid4021426 |
dtxsid6041426 , |
tox21_301188 |
3,4-dihydro-2h-pyrane |
STL146593 |
nsc 57860 |
einecs 203-810-4 |
ai3-16497 |
unii-t6v9n71ihx |
dihydropyran (van) |
2,3-dihydropyran [un2376] [flammable liquid] |
t6v9n71ihx , |
un2376 |
ec 203-810-4 |
delta2-dihydropyran |
BP-21473 |
3,4-dihdro-2h-pyrane |
3,4-dihydro-2 h-pyran |
2,3-dihydro-pyran |
3,4-dihydro-2-pyran |
3,4-dihydro-2-h-pyrane |
3,4-dihydropyrane |
3.4-dihydro-2h-pyran |
2,4-dihydropyran |
3,4- dihydro-2h-pyran |
dihyropyran |
2,3-dihydro-4-h-pyran |
3,4dihydro-2h-pyran |
3,4-dihyro-2h-pyran |
3,4 - dihydro-2h-pyran |
3,4-dihydro-pyran |
3,4-dihydro-2h -pyran |
dihyrdopyran |
3,4-dihydro 2h-pyran |
2,3dihydropyran |
3,4-dihydro-1h-pyran |
2,3-dihyropyran |
3,4-dihydro-[2h]-pyran |
3,4-dihydro-2-h-pyran |
3,4 dihydro-2h-pyran |
3, 4dihydro-2h-pyran |
3,4-dihydro-2h pyran |
2,3-dihydro-4h-pyrane |
4,5-dihydropyran |
3,4-dihydro(2h)pyran |
STR01188 |
CS-W013755 |
pyran, dihydro- |
2,3-dihydro-.gamma.-pyran |
2-pyran, 3,4-dihydro- |
1,2-pyran, 3,4-dihydro- |
dihydro-2h-pyran, 3,4- |
dihydropyran [mi] |
CHEMBL3184439 |
mfcd00006558 |
J-511179 |
F0001-0228 |
3,4-dihydro-2h-pyran, purum, >=95.0% (gc) |
Q419349 |
AMY39440 |
D78128 |
EN300-26571 |
Protein | Taxonomy | Measurement | Average (µ) | Min (ref.) | Avg (ref.) | Max (ref.) | Bioassay(s) |
---|---|---|---|---|---|---|---|
estrogen nuclear receptor alpha | Homo sapiens (human) | Potency | 14.2680 | 0.0002 | 29.3054 | 16,493.5996 | AID743075; AID743079 |
Cellular tumor antigen p53 | Homo sapiens (human) | Potency | 24.3365 | 0.0023 | 19.5956 | 74.0614 | AID651631 |
[prepared from compound, protein, and bioassay information from National Library of Medicine (NLM), extracted Dec-2023] |
Assay ID | Title | Year | Journal | Article |
---|---|---|---|---|
AID1133201 | Antimicrobial activity against Microsporum canis at 0.4 umol/mL by broth microdilution method | 1978 | Journal of medicinal chemistry, Dec, Volume: 21, Issue:12 | Synthesis and antiviral and enzymatic studies of certain 3-deazaguanines and their imidazolecarboxamide precursors. |
AID1133202 | Antimicrobial activity against Pseudomonas aeruginosa at 0.4 umol/mL by broth microdilution method | 1978 | Journal of medicinal chemistry, Dec, Volume: 21, Issue:12 | Synthesis and antiviral and enzymatic studies of certain 3-deazaguanines and their imidazolecarboxamide precursors. |
AID1133200 | Antimicrobial activity against Epidermophyton floccosum at 0.4 umol/mL by broth microdilution method | 1978 | Journal of medicinal chemistry, Dec, Volume: 21, Issue:12 | Synthesis and antiviral and enzymatic studies of certain 3-deazaguanines and their imidazolecarboxamide precursors. |
AID1133203 | Antimicrobial activity against Staphylococcus aureus at 0.4 umol/mL by broth microdilution method | 1978 | Journal of medicinal chemistry, Dec, Volume: 21, Issue:12 | Synthesis and antiviral and enzymatic studies of certain 3-deazaguanines and their imidazolecarboxamide precursors. |
AID1133198 | Antimicrobial activity against Candida albicans at 0.4 umol/mL by broth microdilution method | 1978 | Journal of medicinal chemistry, Dec, Volume: 21, Issue:12 | Synthesis and antiviral and enzymatic studies of certain 3-deazaguanines and their imidazolecarboxamide precursors. |
AID1133204 | Antimicrobial activity against Trichophyton mentagrophytes at 0.4 umol/mL by broth microdilution method | 1978 | Journal of medicinal chemistry, Dec, Volume: 21, Issue:12 | Synthesis and antiviral and enzymatic studies of certain 3-deazaguanines and their imidazolecarboxamide precursors. |
[information is prepared from bioassay data collected from National Library of Medicine (NLM), extracted Dec-2023] |
Timeframe | Studies, This Drug (%) | All Drugs % |
---|---|---|
pre-1990 | 1 (11.11) | 18.7374 |
1990's | 1 (11.11) | 18.2507 |
2000's | 1 (11.11) | 29.6817 |
2010's | 6 (66.67) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |
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.
| This Compound (28.43) All Compounds (24.57) |
Publication Type | This drug (%) | All Drugs (%) |
---|---|---|
Trials | 0 (0.00%) | 5.53% |
Reviews | 0 (0.00%) | 6.00% |
Case Studies | 0 (0.00%) | 4.05% |
Observational | 0 (0.00%) | 0.25% |
Other | 9 (100.00%) | 84.16% |
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023] |