Bromide

Bromide

SCHEMBL351809

Br.c1ccc(-c2nnnn2-c2ccccc2)cc1

nearest known ligand 0.74

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
ACHE known ✓ P22303 1/20 0.48
LMNA P02545 4/20 0.74
HSD17B10 Q99714 1/20 0.74
ALDH1A1 P00352 8/20 0.72
L3MBTL1 Q9Y468 3/20 0.72
PTGS2 P35354 3/20 0.64
SMN1; SMN2 Q16637 3/20 0.64
PKM P14618 1/20 0.64
TSHR P16473 6/20 0.63
MEN1 O00255 2/20 0.57
KMT2A Q03164 2/20 0.57
MAPK10 P53779 1/20 0.51
NPSR1 Q6W5P4 3/20 0.50
MAPT P10636 2/20 0.50
HTT P42858 2/20 0.50
HPGD P15428 1/20 0.50
CCR6 P51684 1/20 0.50
CACNA1B Q00975 1/20 0.50
APBA1 Q02410 1/20 0.50
TDP1 Q9NUW8 1/20 0.50

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 SCHEMBL28098177 1.00 LMNA (0.74) LMNAHSD17B10ALDH1A1L3MBTL1PTGS2
SCHEMBL890039 0.98 LMNA (0.77) LMNAHSD17B10ALDH1A1L3MBTL1PTGS2
Hydrochloric Acid SCHEMBL7981337 0.96 LMNA (0.74) LMNAHSD17B10ALDH1A1L3MBTL1PTGS2
SCHEMBL11531369 0.89 ALDH1A1 (0.70) LMNAHSD17B10ALDH1A1L3MBTL1PTGS2
Urea SCHEMBL28915393 0.88 PTGS2 (0.64) LMNAHSD17B10ALDH1A1L3MBTL1PTGS2
SCHEMBL11536760 0.87 ALDH1A1 (0.65) LMNAHSD17B10ALDH1A1L3MBTL1PTGS2
SCHEMBL15452507 0.87 ALDH1A1 (0.71) LMNAHSD17B10ALDH1A1L3MBTL1PTGS2
SCHEMBL8534360 0.85 LMNA (0.71) LMNAHSD17B10ALDH1A1L3MBTL1PTGS2
Hydrochloric Acid SCHEMBL5459649 0.85 L3MBTL1 (0.73) LMNAHSD17B10ALDH1A1L3MBTL1PTGS2
SCHEMBL15541266 0.85 ALDH1A1 (0.63) LMNAHSD17B10ALDH1A1L3MBTL1PTGS2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-108440433-A The method that copper lewis acid Surfactant-Catalyzed prepares chlorination -3- substitution -2,5- diphenyltetrazolium bromides 湖北佰智昂生物化工有限公司 2018-08-24 CN claimed
US-9354239-B2 BLID; protein domain for interaction with the Bcl-2 family of proteins WITTE-HOFFMANN CARLOS (US) 2016-05-31 US claimed
US-9346868-B2 BLID; a novel protein domain for interaction with the Bcl-2 family of proteins. Applications in oncology WITTE-HOFFMANN CARLOS (US) 2016-05-24 US claimed
EP-0720657-B1 BIOLOGICALLY RELEVANT METHODS FOR THE RAPID DETERMINATION OF STERILITY 3M INNOVATIVE PROPERTIES CO (US) 2007-08-15 EP claimed
EP-0720657-A4 BIOLOGICALLY RELEVANT METHODS FOR THE RAPID DETERMINATION OF STERILITY 3M INNOVATIVE PROPERTIES CO (US) 2004-08-04 EP claimed
EP-0720657-A1 BIOLOGICALLY RELEVANT METHODS FOR THE RAPID DETERMINATION OF STERILITY NORTH AMERICAN SCIENCE ASSOCIATES INCORPORATED (US) 1996-07-10 EP claimed
US-5486459-A Biologically relevant methods for the rapid determination of sterility MEDICAL COLLEGE OF OHIO (US) 1996-01-23 US claimed
WO-1995008639-A1 BIOLOGICALLY RELEVANT METHODS FOR THE RAPID DETERMINATION OF STERILITY NORTH AMERICAN SCIENCE ASSOCIATES, INC. (US) 1995-03-30 WO claimed
EP-4712993-A2 PHAGE THERAPY FOR ALCOHOL-ASSOCIATED HEPATITIS The Regents of the University of California (US) 2026-03-25 EP disclosed
US-20260001910-A1 PEPTIDES AND USES THEREOF PREVECEUTICAL MEDICAL INC (CA) 2026-01-01 US disclosed
WO-2025215115-A1 COMPOUNDS FOR USE THE TREATMENT OF CANCER, NEURODEGENERATIVE DISEASES, PSYCHIATRIC DISORDERS, INFLAMMATION, EPILEPSY AND SEIZURES B&A ONCOMEDICAL (FR) 2025-10-16 WO disclosed
CN-120136932-A Metal compound capable of improving stability and preparation method and application thereof 浙江海利得新材料股份有限公司 2025-06-13 CN disclosed
CN-120081885-A Substituted phenyl glycoside compound and preparation method and application thereof 浙江大学 2025-06-03 CN disclosed
CN-119950489-A Nanoparticle for inducing iron death as well as preparation method and application thereof 三亚中心医院(海南省第三人民医院、三亚中心医院医疗集团总院) 2025-05-09 CN disclosed
WO-1994014064-A1 METHODOLOGY FOR DEVELOPING A SUPERIOR LINE OF DOMESTICATED ANIMALS UNIVERSITY OF GUELPH (CA) 1994-06-23 WO disclosed
EP-0532636-A4 BIS-NAPHTHALIMIDES AS ANTICANCER AGENTS 1993-11-18 EP disclosed
EP-0532636-A1 BIS-NAPHTHALIMIDES AS ANTICANCER AGENTS THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1993-03-24 EP disclosed
WO-1991018884-A1 BIS-NAPHTHALIMIDES AS ANTICANCER AGENTS THE DU PONT MERCK PHARMACEUTICAL COMPANY (US) 1991-12-12 WO disclosed
EP-0426167-A2 Antitumor substance, process for preparing the same, and pharmaceutical composition containing the same MEIJI SEIKA KAISHA LTD. (JP) 1991-05-08 EP disclosed
EP-0418113-A2 Microbiological assay kit and method for detecting antibacterial compounds ORGENICS LIMITED (IL) 1991-03-20 EP 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 (1 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-20260001910-A1 PEPTIDES AND USES THEREOF MMP3, PEPD, MMP9 ACHE 2551/4885LMNA 1535/4885HSD17B10 2427/4885

“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.