| Nome |
# |
|
N-Acylbenzenesulfonamide dihydro-1,3,4-oxadiazole hybrids: seeking selectivity toward carbonic anhydrase isoforms, file e2f56ed6-c93d-3eaf-e053-3a05fe0a5d97
|
635
|
|
Investigating the Anticancer Activity of Isatin/Dihydropyrazole Hybrids, file e2f56ed8-0acd-3eaf-e053-3a05fe0a5d97
|
525
|
|
Isatin thiazoline hybrids as dual inhibitors of HIV-1 reverse transcriptase, file e2f56ed6-c1d3-3eaf-e053-3a05fe0a5d97
|
138
|
|
Exploring new structural features of the 4-[(3-methyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzenesulphonamide scaffold for the inhibition of human carbonic anhydrases, file e2f56ed8-8409-3eaf-e053-3a05fe0a5d97
|
133
|
|
Limonoids from Melia azedarach fruits as inhibitors of flaviviruses and mycobacterium tubercolosis, file e2f56ed5-734b-3eaf-e053-3a05fe0a5d97
|
117
|
|
Coumarins from Magydaris pastinacea as inhibitors of the tumour-associated carbonic anhydrases IX and XII: isolation, biological studies and in silico evaluation, file e2f56ed8-d9af-3eaf-e053-3a05fe0a5d97
|
106
|
|
New Dihydrothiazole Benzensulfonamides: Looking for Selectivity toward Carbonic Anhydrase Isoforms I, II, IX, and XII, file e2f56ed9-cafd-3eaf-e053-3a05fe0a5d97
|
83
|
|
Natural product-inspired esters and amides of ferulic and caffeic acid as dual inhibitors of HIV-1 reverse transcriptase, file 6ab46032-462e-47f0-bffe-1cded7d2e748
|
67
|
|
Exploring new scaffolds for the dual inhibition of HIV-1 RT polymerase and ribonuclease associated functions, file e2f56eda-222c-3eaf-e053-3a05fe0a5d97
|
60
|
|
(3Z)-3-(2-[4-(aryl)-1,3-thiazol-2-yl]hydrazin-1-ylidene)-2,3-dihydro- 1H -indol-2-one derivatives as dual inhibitors of HIV-1 reverse transcriptase, file e04e01a7-d295-4712-b05a-1faf6cc4ad84
|
54
|
|
Phenylpropenoids from Bupleurum fruticosum as Anti-Human Rhinovirus Species A Selective Capsid Binders, file aff2fd12-4dcd-4a95-a61d-85e67eb8517d
|
41
|
|
Effects of docosanyl ferulate, a constituent of Withania somnifera, on ethanol- and morphine-elicited conditioned place preference and ERK phosphorylation in the accumbens shell of CD1 mice, file e2f56eda-3ef0-3eaf-e053-3a05fe0a5d97
|
31
|
|
Flavonoids and Acid-Hydrolysis derivatives of Neo-Clerodane diterpenes from Teucrium flavum subsp. glaucum as inhibitors of the HIV-1 reverse transcriptase–associated RNase H function, file e2f56eda-0989-3eaf-e053-3a05fe0a5d97
|
30
|
|
Targeting tumor associated carbonic anhydrase IX and XII: Highly isozyme selective coumarin and psoralen inhibitors, file 52a060e5-f0f7-41cf-874f-b412c75f203f
|
26
|
|
Selective inhibition of carbonic anhydrase IX and XII by coumarin and psoralen derivatives, file e2f56eda-2aa3-3eaf-e053-3a05fe0a5d97
|
26
|
|
Natural product-inspired esters and amides of ferulic and caffeic acid as dual inhibitors of HIV-1 reverse transcriptase, file e2f56ed6-52ca-3eaf-e053-3a05fe0a5d97
|
17
|
|
5-Nitro-3-(2-(4-phenylthiazol-2-yl)hydrazineylidene)indolin-2-one derivatives inhibit HIV-1 replication by a multitarget mechanism of action, file 8362faad-16eb-4d5f-8845-2fa29ef1697b
|
14
|
|
Design, synthesis, and biological evaluation of 1,3-diarylpropenones as dual inhibitors of HIV-1 reverse transcriptase, file e2f56ed3-8eb6-3eaf-e053-3a05fe0a5d97
|
12
|
|
Exploring the thiazole scaffold for the identification of new agents for the treatment of fluconazole resistant Candida, file e2f56ed4-f856-3eaf-e053-3a05fe0a5d97
|
9
|
|
Formulation and In Vitro Efficacy Assessment of Teucrium marum Extract Loading Hyalurosomes Enriched with Tween 80 and Glycerol, file e2f56eda-d0d0-3eaf-e053-3a05fe0a5d97
|
9
|
|
Floral markers of strawberry tree (Arbutus unedo L.) honey, file e2f56ed3-be98-3eaf-e053-3a05fe0a5d97
|
8
|
|
Drug design, synthesis, in vitro and in silico evaluation of selective monoaminoxidase B inhibitors based on 3-acetyl-2-dichlorophenyl-5-aryl-2,3-dihydro-1,3,4-oxadiazole chemical scaffold, file e2f56ed5-9d6f-3eaf-e053-3a05fe0a5d97
|
8
|
|
null, file e2f56ed3-c949-3eaf-e053-3a05fe0a5d97
|
7
|
|
Withania somnifera prevents acquisition and expression of morphine-elicited conditioned place preference, file e2f56ed5-1c48-3eaf-e053-3a05fe0a5d97
|
7
|
|
Phenylpropenoids from Bupleurum fruticosum as Anti-Human Rhinovirus Species A Selective Capsid Binders, file e2f56ed7-0026-3eaf-e053-3a05fe0a5d97
|
7
|
|
Suppression of lipopolysaccharide-induced COX-2 expression via p38MAPK, JNK, and C/EBPβ phosphorylation inhibition by furomagydarin A, a benzofuran glycoside from Magydaris pastinacea, file aeb61d46-b980-4f88-863c-75ccc0bc3ff8
|
5
|
|
New 4-[(3-cyclohexyl-4-aryl-2,3-dihydro-1,3-thiazol-2-ylidene)amino]benzene-1-sulfonamides, synthesis and inhibitory activity toward carbonic anhydrase I, II, IX, XII, file e2f56ed5-734a-3eaf-e053-3a05fe0a5d97
|
5
|
|
Tuning the Dual Inhibition of Carbonic Anhydrase and Cyclooxygenase by Dihydrothiazole Benzensulfonamides, file e2f56ed7-889b-3eaf-e053-3a05fe0a5d97
|
5
|
|
2H-chromene and 7H-furo-chromene derivatives selectively inhibit tumour associated human carbonic anhydrase IX and XII isoforms, file 7091c921-6623-4325-9501-876b1b7d2391
|
4
|
|
Lumichrome and Phenyllactic Acid as Chemical Markers of Thistle (Galactites tomentosa Moench) Honey, file e2f56ed3-c8b4-3eaf-e053-3a05fe0a5d97
|
4
|
|
Cytotoxic phloroglucinols from the leaves of Myrtus communis, file e2f56ed5-eb04-3eaf-e053-3a05fe0a5d97
|
4
|
|
null, file e2f56ed3-bb5c-3eaf-e053-3a05fe0a5d97
|
3
|
|
Withania somnifera root extract prolongs analgesia and suppresses hyperalgesia in mice treated with morphine, file e2f56ed3-bdb6-3eaf-e053-3a05fe0a5d97
|
3
|
|
Phenolic constituents from Ephedra nebrodensis, file e2f56ed3-bf23-3eaf-e053-3a05fe0a5d97
|
3
|
|
Ungeremine effectively targets mammalian as well as bacterial type I and type II
topoisomerases, file e2f56ed3-d8b0-3eaf-e053-3a05fe0a5d97
|
3
|
|
N-Alkyl dien- and trienamides from the roots of Otanthus maritimus with binding affinity for opioid and cannabinoid receptors, file e2f56ed4-dfe3-3eaf-e053-3a05fe0a5d97
|
3
|
|
Through scaffold modification to 3,5-diaryl-4,5-dihydroisoxazoles: new potent and selective inhibitors of monoamine oxidase B, file e2f56ed6-bf4f-3eaf-e053-3a05fe0a5d97
|
3
|
|
Multi-target activity of Hemidesmus indicus decoction against innovative HIV-1 drug targets and characterization of Lupeol mode of action, file e2f56ed6-d1cc-3eaf-e053-3a05fe0a5d97
|
3
|
|
Ferulic Acid Esters and Withanolides: in Search of Withania somnifera GABAA Receptor Modulators, file e2f56ed8-7a68-3eaf-e053-3a05fe0a5d97
|
3
|
|
The biologically active compound of Withania somnifera (L.) Dunal, docosanyl ferulate, is endowed with potent anxiolytic properties but devoid of typical benzodiazepine-like side effects, file e2f56ed9-d44e-3eaf-e053-3a05fe0a5d97
|
3
|
|
null, file e2f56ed3-c616-3eaf-e053-3a05fe0a5d97
|
2
|
|
null, file e2f56ed4-61e0-3eaf-e053-3a05fe0a5d97
|
2
|
|
A chromone from Seseli praecox (Apiaceae), file e2f56ed4-8879-3eaf-e053-3a05fe0a5d97
|
2
|
|
Methoxyflavones from Stachys glutinosa with binding affinity to opioid receptors: in silico, in vitro, and in vivo studies, file e2f56ed5-e9f3-3eaf-e053-3a05fe0a5d97
|
2
|
|
NEW CHROMANONE ACIDS WITH ANTIBACTERIAL ACTIVITY FROM CALOPHYLLUM BRASILIENSE, file e2f56ed3-c905-3eaf-e053-3a05fe0a5d97
|
1
|
|
Antioxidant activity of extracts from plants growing in Sardinia, file e2f56ed5-2a0b-3eaf-e053-3a05fe0a5d97
|
1
|
|
Falcarinol is a covalent cannabinoid CB1 receptor antagonist and induces pro-allergic effects in skin, file e2f56ed5-ed16-3eaf-e053-3a05fe0a5d97
|
1
|
|
Isatin: a privileged scaffold for the design of carbonic anhydrase inhibitors, file e2f56ed6-c774-3eaf-e053-3a05fe0a5d97
|
1
|
| Totale |
2.236 |