Bromide

Bromide

SCHEMBL517469

O=C1c2ccccc2C(=O)N1CCC[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Br-]

nearest known ligand 0.53

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 12)

geneUniProtsupporting neighboursconfidence
▸ CHRM2 known ✓ P08172 1/20 0.50
▸ TDP1 Q9NUW8 1/20 0.53
▸ L3MBTL1 Q9Y468 1/20 0.53
▸ MAPT P10636 1/20 0.53
▸ RAB9A P51151 1/20 0.53
▸ SMN1; SMN2 Q16637 1/20 0.53
▸ CYP1A2 P05177 1/20 0.51
▸ CYP2D6 P10635 1/20 0.51
▸ CYP2C19 P33261 1/20 0.51
▸ CASP3 P42574 1/20 0.49
▸ HDAC1 Q13547 3/20 0.48
▸ HDAC7 Q8WUI4 3/20 0.48

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 SCHEMBL29425571 1.00 TDP1 (0.53) TDP1L3MBTL1MAPTRAB9ASMN1; SMN2
Bromide SCHEMBL1325100 0.95 TDP1 (0.55) TDP1L3MBTL1MAPTRAB9ASMN1; SMN2
Bromide SCHEMBL20541913 0.94 TDP1 (0.58) TDP1L3MBTL1MAPTRAB9ASMN1; SMN2
Bromide SCHEMBL20541546 0.94 TDP1 (0.58) TDP1L3MBTL1MAPTRAB9ASMN1; SMN2
Bromide SCHEMBL20541445 0.94 TDP1 (0.58) TDP1L3MBTL1MAPTRAB9ASMN1; SMN2
Bromide SCHEMBL1579652 0.94 TDP1 (0.58) TDP1L3MBTL1MAPTRAB9ASMN1; SMN2
Bromide SCHEMBL20541389 0.94 TDP1 (0.58) TDP1L3MBTL1MAPTRAB9ASMN1; SMN2
Bromide SCHEMBL6664857 0.90 CASP3 (0.51) TDP1L3MBTL1MAPTRAB9ASMN1; SMN2
SCHEMBL14764997 0.83 TDP1 (0.50) TDP1L3MBTL1CYP1A2CYP2C19CHRM2
Bromide SCHEMBL20541573 0.79 RAB9A (0.56) RAB9ACYP1A2CYP2D6CYP2C19CHRM2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114181039-A Synthetic method of 4, 4-diphenyl-3-buten-1-ol 凯美克(上海)医药科技有限公司 2022-03-15 — — CN claimed
CN-114181039-A Synthetic method of 4, 4-diphenyl-3-buten-1-ol 凯美克(上海)医药科技有限公司 2022-03-15 — — CN disclosed
CN-114181039-A Synthetic method of 4, 4-diphenyl-3-buten-1-ol 凯美克(上海)医药科技有限公司 2022-03-15 — — CN disclosed
EP-3265458-B1 BENZAZEPINE DICARBOXAMIDE COMPOUNDS HOFFMANN LA ROCHE (CH) 2018-12-19 — — EP disclosed
EP-3265458-A1 BENZAZEPINE DICARBOXAMIDE COMPOUNDS F. Hoffmann-La Roche AG (CH) 2018-01-10 — — EP disclosed
US-9822065-B1 Benzazepine dicarboxamide compounds HOFFMANN-LA ROCHE INC. (US) 2017-11-21 — — US disclosed
EP-3144303-A1 6-SUBSTITUTED PHENOXYCHROMAN CARBOXYLIC ACID DERIVATIVES Array Biopharma, Inc. (US) 2017-03-22 — — EP disclosed
US-9597333-B2 Benzazepine dicarboxamide compounds HOFFMANN-LA ROCHE INC. (US) 2017-03-21 — — US disclosed
US-9556139-B2 6-substituted phenoxychroman carboxylic acid derivatives ARRAY BIOPHARMA INC. (US) 2017-01-31 — — US disclosed
US-20170014423-A1 Benzazepine Dicarboxamide Compounds HOFFMANN-LA ROCHE INC. (US) 2017-01-19 — — US disclosed
US-20140005418-A1 6-SUBSTITUTED PHENOXYCHROMAN CARBOXYLIC ACID DERIVATIVES ARRAY BIOPHARMA INC. (US) 2014-01-02 — — US disclosed
US-8569522-B2 6-substituted phenoxychroman carboxylic acid derivatives ARRAY BIOPHARMA INC. (US) 2013-10-29 — — US disclosed
US-20120028971-A1 OXO-HETEROCYCLICALLY SUBSTITUTED ALKYL CARBOXYLIC ACIDS AND USE THEREOF BAYER PHARMA AKTIENGESELLSCHAFT (DE) 2012-02-02 — — US disclosed
EP-2406215-A1 OXO-HETEROCYCLICALLY SUBSTITUTED ALKYL CARBOXYLIC ACIDS AND USE THEREOF Bayer Pharma Aktiengesellschaft (DE) 2012-01-18 — — EP disclosed
US-20110105463-A1 6-SUBSTITUTED PHENOXYCHROMAN CARBOXYLIC ACID DERIVATIVES ARRAY BIOPHARMA INC. (US) 2011-05-05 — — US disclosed
WO-2010102717-A1 OXO-HETEROCYCLICALLY SUBSTITUTED ALKYL CARBOXYLIC ACIDS AND USE THEREOF BAYER SCHERING PHARMA AKTIENGESELLSCHAFT (DE) 2010-09-16 — — WO disclosed
US-7084154-B2 2-(aminomethyl) arylamide analgesics PHARMACOPEIA DRUG DISCLOVERY, INC. (US) 2006-08-01 — — US disclosed
US-20040167119-A1 2-(aminomethyl) arylamide analgesics PHARMACOPEIA, INC (US) 2004-08-26 — — US disclosed
WO-2004071445-A2 2-(AMINOMETHYL)ARYLAMIDE ANALGESICS PHARMACOPEIA DRUG DISCOVERY, INC. (US) 2004-08-26 — — WO disclosed
US-4134918-A ENZYME INHIBITORS, ANTIBODY INHIBITORS MERRELL TORAUDE ET COMPAGNIE (FR) 1979-01-16 — — 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 (5 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-20170014423-A1 Benzazepine Dicarboxamide Compounds TLR1, TLR4, TLR5 CHRM2 448/4885TDP1 2974/4885L3MBTL1 1787/4885
US-20110105463-A1 6-SUBSTITUTED PHENOXYCHROMAN CARBOXYLIC ACID DERIVATIVES GPR52, CD22, CD4 CHRM2 23/4885TDP1 3146/4885L3MBTL1 824/4885
US-20140005418-A1 6-SUBSTITUTED PHENOXYCHROMAN CARBOXYLIC ACID DERIVATIVES UGT1A6, UGT2B7, UGT1A7 CHRM2 1696/4885TDP1 4406/4885L3MBTL1 4797/4885
US-20120028971-A1 OXO-HETEROCYCLICALLY SUBSTITUTED ALKYL CARBOXYLIC ACIDS AND USE THEREOF AADAC, OTC, HCAR2 CHRM2 1624/4885TDP1 2877/4885L3MBTL1 3544/4885
US-20040167119-A1 2-(aminomethyl) arylamide analgesics OPRL1, OPRM1, OPRK1 CHRM2 672/4885TDP1 3650/4885L3MBTL1 2067/4885

“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.

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