Bromide

Bromide

SCHEMBL123536

CC[N+](CC)(CC)c1ccccc1C.[Br-]

nearest known ligand 0.41

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

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 3/20 0.41
CHRM4 known ✓ P08173 1/20 0.33
CHRM1 known ✓ P11229 1/20 0.33
CHRM3 known ✓ P20309 1/20 0.33
TSHR P16473 1/20 0.41
LMNA P02545 1/20 0.34
BLM P54132 1/20 0.34
MAPT P10636 2/20 0.33
ALDH1A1 P00352 2/20 0.33
HTT P42858 1/20 0.33
CA1 P00915 1/20 0.33
CA2 P00918 1/20 0.33
CA7 P43166 1/20 0.33
CA9 Q16790 1/20 0.33
CHRNB2 P17787 2/20 0.32
CHRNB4 P30926 2/20 0.32
CHRNA3 P32297 2/20 0.32
CHRNA7 P36544 2/20 0.32
CHRNA4 P43681 2/20 0.32
TAAR1 Q96RJ0 1/20 0.32

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
SCHEMBL9712027 0.98 ACHE (0.43) ACHETSHRLMNABLMMAPT
Hydrochloric Acid SCHEMBL26110882 0.95 ACHE (0.41) ACHETSHRLMNABLMMAPT
Water SCHEMBL11596575 0.95 ACHE (0.41) ACHETSHRLMNABLMMAPT
Sulfuric Acid SCHEMBL31286317 0.86 LMNA (0.34) ACHETSHRLMNAMAPTALDH1A1
SCHEMBL10777360 0.83 TSHR (0.35) ACHETSHRLMNABLMMAPT
SCHEMBL2486358 0.82 CHRNB4 (0.38) ACHETSHRLMNAALDH1A1CHRM4
Hydrochloric Acid SCHEMBL11126825 0.80 KMT2A (0.42) LMNAALDH1A1HTTCHRM1CHRM3
Water SCHEMBL11439671 0.80 DNM1 (0.40) LMNAALDH1A1HTTCHRM1CHRM3
Hydrochloric Acid SCHEMBL11127290 0.78 KMT2A (0.45) LMNAALDH1A1HTTCHRM1CHRM3
Water SCHEMBL11441211 0.78 DNM1 (0.42) LMNAALDH1A1HTTCHRM1CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250204164-A1 DISPLAY DEVICE AND PHOTOSENSITIVE COMPOSITION TORAY INDUSTRIES, INC. (JP) 2025-06-19 US disclosed
CN-118923228-A Display device and photosensitive composition 东丽株式会社 2024-11-08 CN disclosed
WO-2023190218-A1 DISPLAY DEVICE AND PHOTOSENSITIVE COMPOSITION 東レ株式会社 2023-10-05 WO disclosed
US-8445175-B2 Composition containing hydroxylated condensation resin for forming resist underlayer film NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2013-05-21 US disclosed
EP-2042927-B1 COMPOSITION CONTAINING HYDROXYLATED CONDENSATION RESIN FOR FORMING FILM UNDER RESIST NISSAN CHEMICAL IND LTD (JP) 2012-03-07 EP disclosed
US-20090317740-A1 Composition containing hydroxylated condensation resin for forming resist underlayer film NISSAN CHEMICAL INDUSTRIES, LTD. (JP) 2009-12-24 US disclosed
EP-2042927-A1 COMPOSITION CONTAINING HYDROXYLATED CONDENSATION RESIN FOR FORMING FILM UNDER RESIST Nissan Chemical Industries, Ltd. (JP) 2009-04-01 EP disclosed