Bromide

Bromide

SCHEMBL7216374

Br.CCCc1ccccc1

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
SIGMAR1 known ✓ Q99720 3/20 0.50
CHRM2 known ✓ P08172 1/20 0.48
HTR1A known ✓ P08908 1/20 0.48
ADRA2A known ✓ P08913 1/20 0.48
SLC6A2 known ✓ P23975 1/20 0.48
SLC6A4 known ✓ P31645 1/20 0.48
ADRA1A known ✓ P35348 1/20 0.48
SLC6A3 known ✓ Q01959 1/20 0.48
TP53 P04637 1/20 0.55
ALDH1A1 P00352 2/20 0.52
HPGD P15428 1/20 0.52
ALOX15 P16050 1/20 0.52
ALOX12 P18054 1/20 0.52
CASP1 P29466 1/20 0.52
HSD17B10 Q99714 1/20 0.52
TAAR1 Q96RJ0 3/20 0.50
TDP1 Q9NUW8 2/20 0.50
CYP2A6 P11509 1/20 0.50
HTR2A P28223 1/20 0.50
SMN1; SMN2 Q16637 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 SCHEMBL9265148 0.97 TP53 (0.52) TP53ALDH1A1HPGDALOX15ALOX12
SCHEMBL40575 0.97
SCHEMBL11594885 0.97 TP53 (0.58) TP53ALDH1A1HPGDALOX15ALOX12
Benzene SCHEMBL28308118 0.97 TP53 (0.58) TP53ALDH1A1HPGDALOX15ALOX12
Benzene SCHEMBL3223041 0.97 TP53 (0.58) TP53ALDH1A1HPGDALOX15ALOX12
SCHEMBL10686071 0.94 TP53 (0.55) TP53ALDH1A1HPGDALOX15ALOX12
Hydrochloric Acid SCHEMBL5792976 0.94 TP53 (0.55) TP53ALDH1A1HPGDALOX15ALOX12
Iodide SCHEMBL10910035 0.94 TP53 (0.55) TP53ALDH1A1HPGDALOX15ALOX12
SCHEMBL31498535 0.94 TP53 (0.55) TP53ALDH1A1HPGDALOX15ALOX12
Ammonia Solution, Strong SCHEMBL479482 0.94 TP53 (0.55) TP53ALDH1A1HPGDALOX15ALOX12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106278811-B Synthetic method of p-bromo linear alkylbenzene 华东师范大学 2019-12-17 CN disclosed
CN-106278811-A A kind of synthetic method to bromine linear alkylbenzene (LAB) 华东师范大学 2017-01-04 CN disclosed
US-6548667-B2 For prevention and treatment of diseases caused by overexpression and overactivation of matrix metalloproteinase SAMSUNG ELECTRONICS CO. LTD. (KR) 2003-04-15 US disclosed
US-20020169314-A1 Sulfonamide derivative as a matrix metalloproteinase inhibitor SAMSUNG ELECTRONICS CO. LTD. (KR) 2002-11-14 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 (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-20020169314-A1 Sulfonamide derivative as a matrix metalloproteinase inhibitor MMP9, MMP3, MMP14 SIGMAR1 3318/4885CHRM2 4530/4885HTR1A 3032/4885

“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.