Bromide

Bromide

SCHEMBL221448

Br.NC(=O)C(CO)c1ccccc1

nearest known ligand 0.63

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHEADRA1AADRA1BADRA1DADRA2AADRA2BADRA2CADRB1ADRB2ADRB3APH1AAPH1BCHRM2CHRM3EZH2GRIN2AHTR1AHTR1BHTR1DHTR1FHTR3ANCSTNP2RY12PSEN1PSEN2PSENENSIGMAR1SLC6A2SLC6A3SLC6A4

The experimentally established mechanism targets of Bromide. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SLC6A3 known ✓ Q01959 3/20 0.43
CHRM2 known ✓ P08172 1/20 0.41
ADRA2C known ✓ P18825 1/20 0.41
CHRM3 known ✓ P20309 1/20 0.41
ADRA1A known ✓ P35348 1/20 0.41
EPHX1 P07099 1/20 0.63
CYP2C19 P33261 3/20 0.44
CYP2D6 P10635 2/20 0.44
CYP1A2 P05177 1/20 0.44
PKM P14618 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
NPSR1 Q6W5P4 1/20 0.44
CES2 O00748 1/20 0.43
CES1 P23141 1/20 0.43
DRD3 P35462 2/20 0.43
LMNA P02545 2/20 0.43
ADORA3 P0DMS8 1/20 0.43
EDNRB P24530 1/20 0.43
MAPK1 P28482 1/20 0.43
MC4R P32245 1/20 0.43

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
SCHEMBL6359024 0.98 EPHX1 (0.66) EPHX1CYP2C19CYP2D6CYP1A2PKM
SCHEMBL23977 0.98 EPHX1 (0.66) EPHX1CYP2C19CYP2D6CYP1A2PKM
SCHEMBL27689551 0.98 EPHX1 (0.66) EPHX1CYP2C19CYP2D6CYP1A2PKM
SCHEMBL16881947 0.98 EPHX1 (0.66) EPHX1CYP2C19CYP2D6CYP1A2PKM
Hydrochloric Acid SCHEMBL222654 0.96 EPHX1 (0.63) EPHX1CYP2C19CYP2D6CYP1A2PKM
Lactic Acid SCHEMBL27998199 0.87 EPHX1 (0.54) EPHX1CYP2C19CYP2D6CYP1A2LMNA
Ethylbenzene SCHEMBL27718807 0.86 EPHX1 (0.62) EPHX1CYP2C19CYP1A2LMNAMEN1
Paraben SCHEMBL10942097 0.83 LMNA (0.53) EPHX1CES2CES1LMNAMEN1
Bromide SCHEMBL30809291 0.83 CYP2C19 (0.57) EPHX1CYP2C19CYP2D6SMN1; SMN2LMNA
SCHEMBL7909103 0.82 EPHX1 (0.61) EPHX1CYP2C19CYP2D6CYP1A2PKM

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10123996-B2 Macrocyclic lactone compounds and methods for their use ELIXIR MEDICAL CORPORATION (US) 2018-11-13 US claimed
US-20170119741-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION 2017-05-04 US claimed
CN-105380947-A Macrolide compound and use method thereof ELIXIR MEDICAL CORP 2016-03-09 CN claimed
US-20150352089-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION 2015-12-10 US claimed
US-20130230571-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2013-09-05 US claimed
EP-2624834-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE Elixir Medical Corporation (US) 2013-08-14 EP claimed
EP-1480677-B8 COMPOSITION FOR STABILIZING HYALURONIC ACID CARL ZEISS MEDITEC SAS (FR) 2012-05-23 EP claimed
WO-2012047813-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2012-04-12 WO claimed
EP-1480677-B1 COMPOSITION FOR STABILIZING HYALURONIC ACID IOLTECH (FR) 2012-02-29 EP claimed
US-8088789-B2 Administering hemiketal ring and seco-macrocyclic lactones; immunosuppressive, anti-proliferative, anti-fungal and anti-tumor ELIXIR MEDICAL CORPORATION (US) 2012-01-03 US claimed
US-20100130544-A1 USE OF PARASYMPATHOLYTIC SUBSTANCES TO ENHANCE AND ACCELERATE STEM CELL DIFFERENTIATION, RELATED METHODS AND COMPOSITIONS UNIVERSITA' DEGLI STUDI DI TORINO (IT) 2010-05-27 US claimed
US-20100086579-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2010-04-08 US claimed
WO-2010040064-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2010-04-08 WO claimed
WO-2009114010-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2009-09-17 WO claimed
EP-2026807-A1 USE OF PARASYMPATHOLYTIC SUBSTANCES TO ENHANCE AND ACCELERATE STEM CELL DIFFERENTIATION, RELATED METHOD AND COMPOSITIONS Universita' Degli Studi di Torino (IT) 2009-02-25 EP claimed
US-20080234309-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE ELIXIR MEDICAL CORPORATION (US) 2008-09-25 US claimed
WO-2007135574-A1 USE OF PARASYMPATHOLYTIC SUBSTANCES TO ENHANCE AND ACCELERATE STEM CELL DIFFERENTIATION, RELATED METHOD AND COMPOSITIONS UNIVERSITA' DEGLI STUDI DI TORINO (IT) 2007-11-29 WO claimed
EP-1480677-A2 COMPOSITION FOR STABILIZING HYALURONIC ACID IOLTECH (FR) 2004-12-01 EP claimed
US-20030133986-A1 Compositions for stabilizing poly (carboxylic acids) TSAO FU-PAO (US) 2003-07-17 US claimed
WO-2003043660-A2 COMPOSITION FOR STABILIZING HYALURONIC ACID NOVARTIS AG (CH) 2003-05-30 WO claimed

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

For each of this compound's patents that has machine-readable text (5 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-10123996-B2 Macrocyclic lactone compounds and methods for their use CHRM2, CHRM1, CHRM5 SLC6A3 4136/4885CHRM2 1/4885ADRA2C 1406/4885
US-20170119741-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE CHRM2, CHRM1, CHRM5 SLC6A3 3439/4885CHRM2 1/4885ADRA2C 1405/4885
US-20150352089-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE CHRM2, CHRM1, CHRM5 SLC6A3 3482/4885CHRM2 1/4885ADRA2C 1422/4885
US-20080234309-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE CHRM2, CHRM1, CHRM5 SLC6A3 3439/4885CHRM2 1/4885ADRA2C 1405/4885
US-20100086579-A1 MACROCYCLIC LACTONE COMPOUNDS AND METHODS FOR THEIR USE VIP, MIF, MYLK SLC6A3 4881/4885CHRM2 1578/4885ADRA2C 3549/4885

“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.