Bromide

Bromide

SCHEMBL949591

Br.Clc1ccc2c(c1)CNC2

nearest known ligand 0.67

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
ADRB1 known ✓ P08588 1/20 0.39
HTR1A known ✓ P08908 1/20 0.39
ADRA2A known ✓ P08913 1/20 0.39
ADRA2B known ✓ P18089 1/20 0.39
ADRA2C known ✓ P18825 1/20 0.39
SLC6A2 known ✓ P23975 1/20 0.39
SLC6A4 known ✓ P31645 1/20 0.39
PNMT P11086 4/20 0.67
HTR2C P28335 6/20 0.54
HTR2A P28223 5/20 0.54
HTR2B P41595 4/20 0.54
ASIC3 Q9UHC3 1/20 0.43
AHR P35869 2/20 0.39
CMA1 P23946 1/20 0.39
CHRNB2 P17787 1/20 0.39
CHRNA4 P43681 1/20 0.39
CNR1 P21554 1/20 0.39
HRH1 P35367 1/20 0.39
KCNH2 Q12809 1/20 0.39
HTR5A P47898 1/20 0.39

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
SCHEMBL329312 0.98 PNMT (0.69) PNMTHTR2CHTR2AHTR2BASIC3
Hydrochloric Acid SCHEMBL383414 0.95 PNMT (0.67) PNMTHTR2CHTR2AHTR2BASIC3
Hydrochloric Acid SCHEMBL16033643 0.93 PNMT (0.64) PNMTHTR2CHTR2AHTR2BASIC3
SCHEMBL532012 0.80 PNMT (0.85) PNMTHTR2CHTR2AHTR2BASIC3
SCHEMBL29543416 0.80 ASIC3 (0.56) PNMTHTR2CHTR2AHTR2BASIC3
SCHEMBL329775 0.80 PNMT (1.00) PNMTHTR2CHTR2AHTR2BASIC3
SCHEMBL29587836 0.80 PNMT (1.00) PNMTHTR2CHTR2AHTR2BASIC3
Hydrochloric Acid SCHEMBL947776 0.79 PNMT (0.81) PNMTHTR2CHTR2AHTR2BASIC3
Hydrochloric Acid SCHEMBL1124954 0.79 PNMT (0.96) PNMTHTR2CHTR2AHTR2BASIC3
SCHEMBL25207974 0.77 PNMT (0.79) PNMTHTR2CHTR2AHTR2BASIC3

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
CN-112218869-A Modulators of integrated stress pathways 卡里科生命科学有限责任公司 2021-01-12 CN disclosed
CN-112166113-A Modulators of integrated stress pathways 卡里科生命科学有限责任公司 2021-01-01 CN disclosed
EP-2931721-B1 THIAZOLE DERIVATIVES AS INHIBITORS OF BRUTON'S TYROSINE KINASE HOFFMANN LA ROCHE (CH) 2016-10-26 EP disclosed
US-9359345-B2 Thiazole derivatives as inhibitors of Bruton's tyrosine kinase HOFFMANN-LA ROCHE INC. (US) 2016-06-07 US disclosed
US-20150353534-A1 THIAZOLE DERIVATIVES AS INHIBITORS OF BRUTON'S TYROSINE KINASE HOFFMANN-LA ROCHE INC. 2015-12-10 US disclosed
EP-2931721-A1 THIAZOLE DERIVATIVES AS INHIBITORS OF BRUTON'S TYROSINE KINASE F.HOFFMANN-LA ROCHE AG (CH) 2015-10-21 EP disclosed
WO-2014090715-A1 THIAZOLE DERIVATIVES AS INHIBITORS OF BRUTON'S TYROSINE KINASE F. HOFFMANN-LA ROCHE AG (CH) 2014-06-19 WO disclosed
US-20110009389-A1 IMIDAZOLE DERIVATIVE, THEIR PRODUCTION AND USE TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2011-01-13 US disclosed
US-20070004736-A1 Imidazole derivative, process for producing the same, and use TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2007-01-04 US disclosed
EP-1564213-A1 IMIDAZOLE DERIVATIVE, PROCESS FOR PRODUCING THE SAME, AND USE Takeda Pharmaceutical Company Limited (JP) 2005-08-17 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 (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-20070004736-A1 Imidazole derivative, process for producing the same, and use HRH4, F2, HRH2 ADRB1 515/4885HTR1A 116/4885ADRA2A 964/4885
US-20110009389-A1 IMIDAZOLE DERIVATIVE, THEIR PRODUCTION AND USE F2, H1-3, CYC1 ADRB1 731/4885HTR1A 298/4885ADRA2A 1464/4885
US-20150353534-A1 THIAZOLE DERIVATIVES AS INHIBITORS OF BRUTON'S TYROSINE KINASE BTK, SYK, LYN ADRB1 1396/4885HTR1A 4379/4885ADRA2A 3629/4885

“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.