Bromide

Bromide

SCHEMBL653935

Br.Br.CC[N+](CC)(CC)Cc1ccccc1.[Br-]

nearest known ligand 0.50

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 19)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 1/20 0.43
CHRNA7 P36544 6/20 0.50
CHRNB4 P30926 5/20 0.50
CHRNA3 P32297 5/20 0.50
KDM4E B2RXH2 1/20 0.50
ALDH1A1 P00352 1/20 0.50
TDP1 Q9NUW8 1/20 0.50
CYP1A2 P05177 1/20 0.47
TP53 P04637 2/20 0.46
DNM1 Q05193 2/20 0.46
NPSR1 Q6W5P4 1/20 0.44
BCHE P06276 1/20 0.43
MEN1 O00255 2/20 0.41
KMT2A Q03164 2/20 0.41
MAPK1 P28482 1/20 0.41
SMN1; SMN2 Q16637 1/20 0.41
CHRNB2 P17787 3/20 0.41
CHRNA4 P43681 3/20 0.41
HTT P42858 2/20 0.40

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
Bromide SCHEMBL27755088 0.98 CHRNA7 (0.49) CHRNA7CHRNB4CHRNA3KDM4EALDH1A1
Bromide SCHEMBL28298658 0.98 CHRNA7 (0.49) CHRNA7CHRNB4CHRNA3KDM4EALDH1A1
Bromide SCHEMBL117943 0.98 KDM4E (0.52) CHRNA7CHRNB4CHRNA3KDM4EALDH1A1
Bromide SCHEMBL653934 0.98 KDM4E (0.52) CHRNA7CHRNB4CHRNA3KDM4EALDH1A1
Bromide SCHEMBL28097171 0.98 KDM4E (0.52) CHRNA7CHRNB4CHRNA3KDM4EALDH1A1
Bromide SCHEMBL653936 0.98 KDM4E (0.52) CHRNA7CHRNB4CHRNA3KDM4EALDH1A1
Water SCHEMBL3646710 0.95 CHRNA7 (0.50) CHRNA7CHRNB4CHRNA3KDM4EALDH1A1
Bromide SCHEMBL3641371 0.95 KDM4E (0.56) CHRNA7CHRNB4CHRNA3KDM4EALDH1A1
Bromide SCHEMBL28903213 0.95 KDM4E (0.50) CHRNA7CHRNB4CHRNA3KDM4EALDH1A1
Hydrochloric Acid SCHEMBL3641370 0.95 CHRNA7 (0.50) CHRNA7CHRNB4CHRNA3KDM4EALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-109836425-B Preparation process of synthetic pemetrexed 江苏创诺制药有限公司 2023-01-24 CN claimed
CN-109836425-B Preparation process of synthetic pemetrexed 江苏创诺制药有限公司 2023-01-24 CN disclosed
CN-107785179-B Preparation method of bromide capacitor positive plate 横店集团东磁股份有限公司 2020-09-29 CN disclosed
CN-107785177-B Bromide capacitor positive electrode slurry and preparation method thereof 横店集团东磁股份有限公司 2020-09-22 CN disclosed
CN-107799768-B Bromide cylindrical battery and assembling method thereof 横店集团东磁股份有限公司 2020-07-31 CN disclosed
CN-107799766-B Bromide soft package battery and assembling method thereof 横店集团东磁股份有限公司 2020-07-28 CN disclosed
CN-107785572-B Bromide square battery and assembling method thereof 横店集团东磁股份有限公司 2020-07-28 CN disclosed
CN-107666008-B Bromide battery positive plate and preparation method thereof 横店集团东磁股份有限公司 2020-07-17 CN disclosed
US-8119808-B2 Tetrahydroquinoline derivatives as cannabinoid receptor modulators BRISTOL-MYERS SQUIBB COMPANY (US) 2012-02-21 US disclosed
US-20110104315-A1 TETRAHYDROQUINOLINE DERIVATIVES AS CANNABINOID RECEPTOR MODULATORS BRISTOL-MYERS SQUIBB COMPANY 2011-05-05 US disclosed
CN-101228146-A Benzofuran derivatives with therapeutic activities PHARMOS CORP (US) 2008-07-23 CN disclosed
EP-1644335-A4 TETRAHYDROQUINOLINE DERIVATIVES AS CANNABINOID RECEPTOR MODULATORS BRISTOL MYERS SQUIBB CO (US) 2008-06-04 EP disclosed
EP-1885709-A2 BENZOFURAN DERIVATIVES WITH THERAPEUTIC ACTIVITIES Pharmos Corporation (US) 2008-02-13 EP disclosed
US-20070099950-A1 Pyridin-4-ylamine compounds useful in the treatment of neuropathic pain AGT SCIENCE LIMITED (GB) 2007-05-03 US disclosed
WO-2006129318-A2 BENZOFURAN DERIVATIVES WITH THERAPEUTIC ACTIVITIES PHARMOS CORPORATION (US) 2006-12-07 WO disclosed
EP-1687275-A1 PYRIDIN-4-YLAMINE COMPOUNDS USEFUL IN THE TREATMENT OF NEUROPATHIC PAIN Merck & Co., Inc. (US) 2006-08-09 EP disclosed
EP-1644335-A1 TETRAHYDROQUINOLINE DERIVATIVES AS CANNABINOID RECEPTOR MODULATORS Bristol-Myers Squibb Company (US) 2006-04-12 EP disclosed
WO-2005051915-A1 PYRIDIN-4-YLAMINE COMPOUNDS USEFUL IN THE TREATMENT OF NEUROPATHIC PAIN MERCK & CO., INC. (US) 2005-06-09 WO disclosed
WO-2005007628-A1 TETRAHYDROQUINOLINE DERIVATIVES AS CANNABINOID RECEPTOR MODULATORS BRISTOL-MYERS SQUIBB COMPANY (US) 2005-01-27 WO disclosed
US-20050014786-A1 Tetrahydroquinoline derivatives as cannabinoid receptor modulators BRISTOL-MYERS SQUIBB COMPANY 2005-01-20 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 (3 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-20110104315-A1 TETRAHYDROQUINOLINE DERIVATIVES AS CANNABINOID RECEPTOR MODULATORS CNR2, CNR1, OPRL1 ACHE 771/4885CHRNA7 169/4885CHRNB4 469/4885
US-20050014786-A1 Tetrahydroquinoline derivatives as cannabinoid receptor modulators CNR2, CNR1, OPRL1 ACHE 771/4885CHRNA7 169/4885CHRNB4 469/4885
US-20070099950-A1 Pyridin-4-ylamine compounds useful in the treatment of neuropathic pain PER2, CNR2, OPRD1 ACHE 988/4885CHRNA7 41/4885CHRNB4 29/4885

“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.