Bromide

Bromide

SCHEMBL414531

Br.Br.Br.CN(C)Cc1ccccc1.CN(C)Cc1ccccc1.CN(C)Cc1ccccc1

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
ADRA2B known ✓ P18089 1/20 0.50
ADRA2C known ✓ P18825 1/20 0.50
SLC6A2 known ✓ P23975 1/20 0.50
SLC6A4 known ✓ P31645 1/20 0.50
ADRA1A known ✓ P35348 1/20 0.50
SLC6A3 known ✓ Q01959 1/20 0.50
SIGMAR1 known ✓ Q99720 1/20 0.47
TSHR P16473 3/20 0.94
ALDH1A1 P00352 2/20 0.94
TAAR1 Q96RJ0 2/20 0.70
AOC3 Q16853 1/20 0.61
HRH3 Q9Y5N1 1/20 0.59
CARM1 Q86X55 1/20 0.52
PRMT6 Q96LA8 1/20 0.52
PRMT8 Q9NR22 1/20 0.52
CHRNB2 P17787 1/20 0.52
CHRNA4 P43681 1/20 0.52
NPC1 O15118 2/20 0.50
RAB9A P51151 2/20 0.50
LMNA P02545 2/20 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 SCHEMBL534887 1.00 TSHR (0.94) TSHRALDH1A1TAAR1AOC3HRH3
Bromide SCHEMBL414532 1.00 TSHR (0.94) TSHRALDH1A1TAAR1AOC3HRH3
Benzene SCHEMBL27653708 1.00 TSHR (0.94) TSHRALDH1A1TAAR1AOC3HRH3
SCHEMBL15900 0.97 TSHR (1.00) TSHRALDH1A1TAAR1AOC3HRH3
SCHEMBL27766437 0.97 TSHR (1.00) TSHRALDH1A1TAAR1AOC3HRH3
SCHEMBL24735547 0.97 TSHR (1.00) TSHRALDH1A1TAAR1AOC3HRH3
SCHEMBL5014268 0.97 TSHR (1.00) TSHRALDH1A1TAAR1AOC3HRH3
Ammonia Solution, Strong SCHEMBL4071832 0.94 TSHR (0.94) TSHRALDH1A1TAAR1AOC3HRH3
Iodide SCHEMBL6672021 0.94 TSHR (0.94) TSHRALDH1A1TAAR1AOC3HRH3
Hydrochloric Acid SCHEMBL6391891 0.94 TSHR (0.94) TSHRALDH1A1TAAR1AOC3HRH3

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8575357-B2 Substituted (thiazolyl-carbonyl)imidazolidinones and use thereof AICURIS GMBH & CO. KG (DE) 2013-11-05 US disclosed
US-8546438-B2 Substituted (thiophenyl-carbonyl)imidazolidinones, and use thereof BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2013-10-01 US disclosed
CN-1989122-B Novel cyclopenta [ b ] benzofuran derivatives and uses thereof INTERMED DISCOVERY GMBH 2013-07-24 CN disclosed
US-20130045999-A1 SUBSTITUTED (THIAZOLYL-CARBONYL)IMIDAZOLIDINONES AND USE THEREOF AICURIS GMBH & CO. KG (DE) 2013-02-21 US disclosed
US-8324268-B2 Substituted furancarboxamides, and use thereof AICURIS GMBH & CO. KG (DE) 2012-12-04 US disclosed
US-20120022059-A1 SUBSTITUTED FURANCARBOXAMIDES, AND USE THEREOF AICURIS GMBH & CO. KG (DE) 2012-01-26 US disclosed
US-20120022123-A1 SUBSTITUTED (THIOPHENYL-CARBONYL)IMIDAZOLIDINONES, AND USE THEREOF AICURIS GMBH & CO. KG (DE) 2012-01-26 US disclosed
US-8030347-B2 Cylopenta[b]benzofuran derivatives and the utilization thereof BAYER HEALTHCARE AG (DE) 2011-10-04 US disclosed
US-20090018113-A1 Novel Cylopenta[B]Benzofuran Derivatives and the Utilization Thereof BAYER HEALTHCARE AG (DE) 2009-01-15 US disclosed
CN-1989122-A Novel cyclopenta [ b ] benzofuran derivatives and uses thereof BAYER HEALTHCARE AG (DE) 2007-06-27 CN 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-20130045999-A1 SUBSTITUTED (THIAZOLYL-CARBONYL)IMIDAZOLIDINONES AND USE THEREOF TPMT, AADAC, PAICS ADRA2B 4411/4885ADRA2C 3279/4885SLC6A2 4501/4885
US-20120022059-A1 SUBSTITUTED FURANCARBOXAMIDES, AND USE THEREOF AADAC, DDC, TPMT ADRA2B 3694/4885ADRA2C 2794/4885SLC6A2 3317/4885
US-20090018113-A1 Novel Cylopenta[B]Benzofuran Derivatives and the Utilization Thereof FKBP1A, FKBP2, FKBP1B ADRA2B 2784/4885ADRA2C 3961/4885SLC6A2 4783/4885
US-20120022123-A1 SUBSTITUTED (THIOPHENYL-CARBONYL)IMIDAZOLIDINONES, AND USE THEREOF TPMT, MAVS, EIF2AK2 ADRA2B 4363/4885ADRA2C 3713/4885SLC6A2 3719/4885

“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.