Bromide

Bromide

SCHEMBL393564

Br.Br.Br.CN(C)c1ccncc1.CN(C)c1ccncc1.CN(C)c1ccncc1

nearest known ligand 0.94

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
CHRM5 P08912 1/20 0.94
CHKA P35790 1/20 0.94
MAPT P10636 4/20 0.68
SMN1; SMN2 Q16637 3/20 0.68
ALOX15 P16050 3/20 0.60
MEN1 O00255 2/20 0.60
KMT2A Q03164 2/20 0.60
NPC1 O15118 1/20 0.60
CASP1 P29466 1/20 0.60
RAB9A P51151 1/20 0.60
HBB P68871 1/20 0.60
ALDH1A1 P00352 7/20 0.56
TSHR P16473 4/20 0.56
HSD17B10 Q99714 2/20 0.56
MAPK1 P28482 3/20 0.43
CYP3A4 P08684 2/20 0.43
TDP1 Q9NUW8 2/20 0.43
TP53 P04637 2/20 0.43
KDM4E B2RXH2 2/20 0.41
GFER P55789 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 SCHEMBL393565 1.00 CHRM5 (0.94) CHRM5CHKAMAPTSMN1; SMN2ALOX15
Bromide SCHEMBL1542160 1.00 CHRM5 (0.94) CHRM5CHKAMAPTSMN1; SMN2ALOX15
Ethane SCHEMBL10432502 0.97 CHRM5 (0.89) CHRM5CHKAMAPTSMN1; SMN2ALOX15
SCHEMBL189 0.97
SCHEMBL8664726 0.97 CHRM5 (1.00) CHRM5CHKAMAPTSMN1; SMN2ALOX15
Bromide SCHEMBL29466744 0.95 CHRM5 (0.84) CHRM5CHKAMAPTSMN1; SMN2ALOX15
Phosphine SCHEMBL23270013 0.94 CHRM5 (0.94) CHRM5CHKAMAPTSMN1; SMN2ALOX15
Hydrochloric Acid SCHEMBL9013636 0.94 CHRM5 (0.94) CHRM5CHKAMAPTSMN1; SMN2ALOX15
SCHEMBL4405649 0.94 CHRM5 (0.94) CHRM5CHKAMAPTSMN1; SMN2ALOX15
Water SCHEMBL19285054 0.94 CHRM5 (0.94) CHRM5CHKAMAPTSMN1; SMN2ALOX15

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250248296-A1 DEFECT ENGINEERING IN WIDE BANDGAP PEROVSKITES FOR EFFICIENT AND STABLE FULLY TEXTURED PEROVSKITE-SILICON TANDEM SOLAR CELLS UNITED STATES DEPARTMENT OF ENERGY 2025-07-31 US claimed
EP-4267591-A2 ORGANOMETALLIC COMPOUNDS Umicore AG & Co. KG (DE) 2023-11-01 EP claimed
WO-2023147338-A2 DEFECT ENGINEERING IN WIDE BANDGAP PEROVSKITES FOR EFFICIENT AND STABLE FULLY TEXTURED PEROVSKITE-SILICON TANDEM SOLAR CELLS THE UNIVERSITY OF NORTH CAROLINA AT CHAPEL HILL (US) 2023-08-03 WO claimed
WO-2022136049-A2 ORGANOMETALLIC COMPOUNDS UMICORE AG & CO. KG (DE) 2022-06-30 WO claimed
US-6248161-B1 Preparation of permanent color inks from water-soluble colorants using specific phosphonium salts HEWLETT-PACKARD COMPANY 2001-06-19 US claimed
US-12552791-B2 Heterocyclic GLP-1 agonists GASHERBRUM BIO, INC. (US) 2026-02-17 US disclosed
EP-4143183-B1 HETEROCYCLIC GLP-1 AGONISTS GASHERBRUM BIO INC (US) 2025-10-22 EP disclosed
US-20250248296-A1 DEFECT ENGINEERING IN WIDE BANDGAP PEROVSKITES FOR EFFICIENT AND STABLE FULLY TEXTURED PEROVSKITE-SILICON TANDEM SOLAR CELLS UNITED STATES DEPARTMENT OF ENERGY 2025-07-31 US disclosed
US-20250214999-A1 HETEROCYCLIC GLP-1 AGONISTS SHOUTI INC. 2025-07-03 US disclosed
CN-112930340-B New synthetic method of piperazinyl-ethoxy-bromophenyl derivatives and their use in the production of compounds containing them 法国施维雅药厂 2025-01-07 CN disclosed
CN-119053608-A Novel compound, conjugated polymer, method for producing same, composition for film formation, organic thin film, and organic semiconductor element 东曹株式会社 2024-11-29 CN disclosed
US-20240116965-A1 ORGANOMETALLIC COMPOUNDS UMICORE AG & CO. KG (DE) 2024-04-11 US disclosed
EP-1250340-A1 METHODS AND COMPOUNDS FOR INHIBITING MRP1 ELI LILLY AND COMPANY (US) 2002-10-23 EP disclosed
EP-1020498-B1 Preparation of permanent color inks from water-soluble colorants using specific phosphonium salts HEWLETT PACKARD CO (US) 2002-10-02 EP disclosed
EP-1226146-A2 QUINOLINE AND NAPHTHYRIDINE CARBOXYLIC ACID ANTIBACTERIALS ABBOTT LABORATORIES (US) 2002-07-31 EP disclosed
US-20020049223-A1 Quinoline and naphthyridine carboxylic acid antibacterials ABBOTT LABORATORIES 2002-04-25 US disclosed
WO-2001046199-A1 METHODS AND COMPOUNDS FOR INHIBITING MRP1 ELI LILLY AND COMPANY (US) 2001-06-28 WO disclosed
US-6248161-B1 Preparation of permanent color inks from water-soluble colorants using specific phosphonium salts HEWLETT-PACKARD COMPANY 2001-06-19 US disclosed
WO-2001032655-A2 QUINOLINE AND NAPHTHYRIDINE CARBOXYLIC ACID ANTIBACTERIALS ABBOTT LABORATORIES (US) 2001-05-10 WO disclosed
EP-1020498-A1 Preparation of permanent color inks from water-soluble colorants using specific phosphonium salts Hewlett-Packard Company (US) 2000-07-19 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 (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-12552791-B2 Heterocyclic GLP-1 agonists GLP1R, NPY1R, NPY2R CHRM5 177/4885CHKA 1391/4885MAPT 4721/4885
US-20020049223-A1 Quinoline and naphthyridine carboxylic acid antibacterials NQO2, NQO1, NDUFA7 CHRM5 3970/4885CHKA 1682/4885MAPT 3354/4885
US-20250214999-A1 HETEROCYCLIC GLP-1 AGONISTS GLP1R, GIPR, GCGR CHRM5 2179/4885CHKA 3402/4885MAPT 3873/4885
US-20240116965-A1 ORGANOMETALLIC COMPOUNDS DDT, PPOX, PDCD2L CHRM5 3711/4885CHKA 3491/4885MAPT 2304/4885

“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.