Bromoenol Lactone

Bromoenol Lactone

SCHEMBL2060001

O=C1O/C(=C/Br)CCC1c1cccc2ccccc12

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
PLA2G6 O60733 4/20 1.00
MAPK1 P28482 3/20 1.00
ALDH1A1 P00352 2/20 1.00
MAPT P10636 2/20 1.00
HPGD P15428 2/20 1.00
BLM P54132 2/20 1.00
NPSR1 Q6W5P4 2/20 1.00
FAAH O00519 1/20 1.00
NPC1 O15118 1/20 1.00
GMNN O75496 1/20 1.00
LMNA P02545 1/20 1.00
MTOR P42345 1/20 1.00
RAB9A P51151 1/20 1.00
SMN1; SMN2 Q16637 1/20 1.00
TRPC5 Q9UL62 1/20 1.00
TRPC6 Q9Y210 1/20 1.00
TP53 P04637 1/20 1.00
CYP3A4 P08684 1/20 1.00
PKM P14618 1/20 1.00
ALOX15 P16050 1/20 1.00

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Bromoenol Lactone SCHEMBL2060074 1.00 PLA2G6 (1.00) PLA2G6MAPK1ALDH1A1MAPTHPGD
(S)-Bromoenol Lactone SCHEMBL3298296 1.00 PLA2G6 (1.00) PLA2G6MAPK1ALDH1A1MAPTHPGD
(S)-Bromoenol Lactone SCHEMBL29693289 1.00 PLA2G6 (1.00) PLA2G6MAPK1ALDH1A1MAPTHPGD
Bromoenol Lactone SCHEMBL29370529 1.00 PLA2G6 (1.00) PLA2G6MAPK1ALDH1A1MAPTHPGD
Bromoenol Lactone SCHEMBL3302140 1.00 PLA2G6 (1.00) PLA2G6MAPK1ALDH1A1MAPTHPGD
Bromoenol Lactone SCHEMBL2060073 1.00 PLA2G6 (1.00) PLA2G6MAPK1ALDH1A1MAPTHPGD
Bromoenol Lactone SCHEMBL3302144 1.00 PLA2G6 (1.00) PLA2G6MAPK1ALDH1A1MAPTHPGD
SCHEMBL3296491 0.89 PLA2G6 (1.00) PLA2G6MAPK1ALDH1A1MAPTHPGD
SCHEMBL3296494 0.89 PLA2G6 (1.00) PLA2G6MAPK1ALDH1A1MAPTHPGD
SCHEMBL3296498 0.89 PLA2G6 (1.00) PLA2G6MAPK1ALDH1A1MAPTHPGD

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 99 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20210236500-A1 INHIBITION OF AUTOPHAGY USING PHOSPHOLIPASE A2 INHIBITORS OREGON HEALTH & SCIENCE UNIVERSITY (US) 2021-08-05 US claimed
US-20190142835-A1 INHIBITION OF AUTOPHAGY USING PHOSPHOLIPASE A2 INHIBITORS OREGON HEALTH & SCIENCE UNIVERSITY (US) 2019-05-16 US claimed
US-8597893-B2 Human phospholipase A2 epsilon WASHINGTON UNIVERSITY IN ST. LOUIS (US) 2013-12-03 US claimed
EP-0954303-B1 METHODS OF TREATING MENTAL DISEASES, INFLAMMATION AND PAIN NEUROSCIENCES RES FOUND (US) 2011-09-21 EP claimed
US-20100183626-A1 HUMAN PHOSPHOLIPASE A2 EPSILON WASHINGTON UNIVERSITY IN ST. LOUIS (US) 2010-07-22 US claimed
US-20070082946-A1 Methods of treating mental diseases, inflammation and pain PIOMELLI DANIELE 2007-04-12 US claimed
US-20060079574-A1 Methods of treating mental diseases, inflammation and pain PIOMELLI DANIELE 2006-04-13 US claimed
US-20050113445-A1 Methods of treating mental diseases, inflammation and pain PIOMELLI DANIELE (US) 2005-05-26 US claimed
US-20030134894-A1 Methods of treating mental diseases, inflammation and pain PIOMELLI DANIELE (US) 2003-07-17 US claimed
US-6525090-B1 Inhibiting the enzyme anandamide amidohydrolase with a haloenol lactone such as 6-(bromomethylene)tetrahydro-3-(1-naphthalenyl)-2H-pyrane-2-one NEUROSCIENCES RESEARCH FOUNDATION, INC. 2003-02-25 US claimed
EP-0954303-A4 METHODS OF TREATING MENTAL DISEASES, INFLAMMATION AND PAIN NEUROSCIENCES RES FOUNDATION (US) 2002-09-18 EP claimed
EP-0954303-A2 METHODS OF TREATING MENTAL DISEASES, INFLAMMATION AND PAIN NEUROSCIENCES RESEARCH FOUNDATION (US) 1999-11-10 EP claimed
US-5925672-A Methods of treating mental diseases, inflammation and pain NEUROSCIENCES RESEARCH FOUNDATION, INC. (US) 1999-07-20 US claimed
WO-1998024396-A2 METHODS OF TREATING MENTAL DISEASES, INFLAMMATION AND PAIN NEUROSCIENCES RESEARCH FOUNDATION, INC. (US) 1998-06-11 WO claimed
US-20230190662-A1 Efficacy of a Gastro-Retentive Bile Acid Sequestrant Dosage Form IRONWOOD PHARMACEUTICALS, INC. 2023-06-22 US disclosed
US-20220370367-A1 Gastro-Retentive Sustained-Release Oral Dosage Form of a Bile Acid Sequestrant IRONWOOD PHARMACEUTICALS INC (US) 2022-11-24 US disclosed
CN-114767646-A Effects of gastric retentive bile acid sequestrant formulation 铁木医药有限公司 2022-07-22 CN disclosed
WO-1998024396-A2 METHODS OF TREATING MENTAL DISEASES, INFLAMMATION AND PAIN NEUROSCIENCES RESEARCH FOUNDATION, INC. (US) 1998-06-11 WO disclosed
US-5707821-A Identification of phospholipase A2 inhibitors in Aβ peptide-mediated neurodegenerative disease ATHENA NEUROSCIENCES, INC. (US) 1998-01-13 US disclosed
US-5208244-A Administering substituted enol lactones WASHINGTON UNIVERSITY (US) 1993-05-04 US disclosed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (4 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20030134894-A1 Methods of treating mental diseases, inflammation and pain APEH, NAAA, FAAH2 PLA2G6 1646/4885MAPK1 2550/4885ALDH1A1 566/4885
US-20060079574-A1 Methods of treating mental diseases, inflammation and pain APEH, FAAH2, NAAA PLA2G6 1840/4885MAPK1 2993/4885ALDH1A1 738/4885
US-20070082946-A1 Methods of treating mental diseases, inflammation and pain APEH, FAAH2, NAAA PLA2G6 1840/4885MAPK1 2993/4885ALDH1A1 738/4885
US-20050113445-A1 Methods of treating mental diseases, inflammation and pain APEH, FAAH2, NAAA PLA2G6 1840/4885MAPK1 2993/4885ALDH1A1 738/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.