Bromide

Bromide

SCHEMBL653936

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

nearest known ligand 0.52

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 0.41
KDM4E B2RXH2 1/20 0.52
ALDH1A1 P00352 1/20 0.52
TDP1 Q9NUW8 1/20 0.52
CYP1A2 P05177 1/20 0.49
TP53 P04637 2/20 0.48
CHRNA7 P36544 6/20 0.47
CHRNB4 P30926 5/20 0.47
CHRNA3 P32297 5/20 0.47
DNM1 Q05193 2/20 0.44
MEN1 O00255 2/20 0.42
KMT2A Q03164 2/20 0.42
MAPK1 P28482 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42
CHRNB2 P17787 3/20 0.42
CHRNA4 P43681 3/20 0.42
HTT P42858 2/20 0.41
BCHE P06276 1/20 0.41
NPSR1 Q6W5P4 1/20 0.41

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 SCHEMBL28097171 1.00 KDM4E (0.52) KDM4EALDH1A1TDP1CYP1A2TP53
Bromide SCHEMBL28298659 0.98 KDM4E (0.50) KDM4EALDH1A1TDP1CYP1A2TP53
Bromide SCHEMBL27697911 0.98 KDM4E (0.50) KDM4EALDH1A1TDP1CYP1A2TP53
Bromide SCHEMBL28903213 0.98 KDM4E (0.50) KDM4EALDH1A1TDP1CYP1A2TP53
Bromide SCHEMBL653935 0.98 CHRNA7 (0.50) KDM4EALDH1A1TDP1CYP1A2TP53
Bromide SCHEMBL27715865 0.98 KDM4E (0.50) KDM4EALDH1A1TDP1CYP1A2TP53
Bromide SCHEMBL3641373 0.98 KDM4E (0.50) KDM4EALDH1A1TDP1CYP1A2TP53
SCHEMBL81238 0.97 KDM4E (0.54) KDM4EALDH1A1TDP1CYP1A2TP53
Hydrogen Sulfide SCHEMBL5998579 0.97 KDM4E (0.54) KDM4EALDH1A1TDP1CYP1A2TP53
Benzene SCHEMBL29130108 0.97 KDM4E (0.54) KDM4EALDH1A1TDP1CYP1A2TP53

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114166921-B Application of chloramine derivatization reagent in double bond position identification 中国科学院上海有机化学研究所 2024-04-26 CN claimed
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-112980046-B Special high-thermal-stability flame retardant for EPS/XPS and preparation method thereof 山东润科化工股份有限公司 2022-04-19 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-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-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-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
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 (2 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-20050014786-A1 Tetrahydroquinoline derivatives as cannabinoid receptor modulators CNR2, CNR1, OPRL1 ACHE 771/4885KDM4E 612/4885ALDH1A1 3577/4885
US-20070099950-A1 Pyridin-4-ylamine compounds useful in the treatment of neuropathic pain PER2, CNR2, OPRD1 ACHE 988/4885KDM4E 699/4885ALDH1A1 2085/4885

“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.