Bromide

Bromide

SCHEMBL3916850

CCCCCCC[N+](CCCC)(CCCC)CCCC.[Br-]

nearest known ligand 0.93

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
▸ ALDH1A1 P00352 1/20 0.93
▸ TP53 P04637 1/20 0.93
▸ CYP3A4 P08684 1/20 0.93
▸ ALOX15 P16050 1/20 0.93
▸ TSHR P16473 1/20 0.93
▸ ALOX12 P18054 1/20 0.93
▸ SMN1; SMN2 Q16637 1/20 0.93
▸ HIF1A Q16665 1/20 0.93
▸ HSD17B10 Q99714 1/20 0.93
▸ SLC22A1 O15245 3/20 0.87
▸ SLC22A2 O15244 1/20 0.80
▸ DNM1 Q05193 7/20 0.78

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 SCHEMBL5084980 1.00 ALDH1A1 (0.93) ALDH1A1TP53CYP3A4ALOX15TSHR
Bromide SCHEMBL5085227 1.00 ALDH1A1 (0.93) ALDH1A1TP53CYP3A4ALOX15TSHR
Bromide SCHEMBL5087210 1.00 ALDH1A1 (0.93) ALDH1A1TP53CYP3A4ALOX15TSHR
Bromide SCHEMBL2733876 1.00 ALDH1A1 (0.93) ALDH1A1TP53CYP3A4ALOX15TSHR
Bromide SCHEMBL5088202 1.00 ALDH1A1 (0.93) ALDH1A1TP53CYP3A4ALOX15TSHR
Bromide SCHEMBL1347880 1.00 ALDH1A1 (0.93) ALDH1A1TP53CYP3A4ALOX15TSHR
Bromide SCHEMBL3028771 1.00 ALDH1A1 (0.93) ALDH1A1TP53CYP3A4ALOX15TSHR
Bromide SCHEMBL8586767 1.00 ALDH1A1 (0.93) ALDH1A1TP53CYP3A4ALOX15TSHR
Bromide SCHEMBL5085187 1.00 ALDH1A1 (0.93) ALDH1A1TP53CYP3A4ALOX15TSHR
Bromide SCHEMBL1507558 1.00 ALDH1A1 (0.93) ALDH1A1TP53CYP3A4ALOX15TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2015180585-A9 METHOD OF PRODUCING THIAMETHOXAM ROTAM AGROCHEM INTERNATIONAL COMPANY LIMITED (CN) 2016-12-15 — — WO claimed
CN-106029658-A Method for preparing thiamethoxam 龙灯农业化工国际有限公司 2016-10-12 — — CN claimed
WO-2015180585-A1 METHOD OF PRODUCING THIAMETHOXAM ROTAM AGROCHEM INTERNATIONAL COMPANY LIMITED (CN) 2015-12-03 — — WO claimed
US-7157006-B2 Method for perchlorate removal from ground water THE PENN STATE RESEARCH FOUNDATION (US) 2007-01-02 — — US claimed
US-20050167366-A1 Method for perchlorate removal from ground water THE PENN STATE RESEARCH FOUNDATION 2005-08-04 — — US claimed
US-6881348-B2 Method for perchlorate removal from ground water THE PENN STATE RESEARCH FOUNDATION (US) 2005-04-19 — — US claimed
US-20030080065-A1 Method for perchlorate removal from ground water THE PENN STATE RESEARCH FOUNDATION 2003-05-01 — — US claimed
WO-2002100509-A1 A METHOD FOR PERCHLORATE REMOVAL FROM GROUND WATER THE PENN STATE RESEARCH FOUNDATION (US) 2002-12-19 — — WO claimed
EP-0743574-B1 Migration imaging members XEROX CORP (US) 2000-12-27 — — EP claimed
EP-0743573-B1 Method for obtaining image contrast migration imaging members XEROX CORP (US) 2000-09-06 — — EP claimed
EP-0615857-B1 Recording sheets containing monoammonium compounds XEROX CORP (US) 1998-11-11 — — EP claimed
EP-0743574-A2 Migration imaging members XEROX CORPORATION (US) 1996-11-20 — — EP claimed
EP-0743573-A2 Method for obtaining image contrast migration imaging members XEROX CORPORATION (US) 1996-11-20 — — EP claimed
US-5563014-A SOFTENABLE LAYER CONTAINIG PHOTOSENSITIVE MARKING MATERIAL; TRANSPARENTIZING AGENT XEROX CORPORATION (US) 1996-10-08 — — US claimed
US-5514505-A SELECTIVE TRANSPARENTIZATION OF PHOTOSENSITIVE MIGRATION MARKING PARTICLES EMBEDDED NEAR THE SURFACE OF A SOFTENABLE LAYER SUPPORTED BY AN ELECTROCONDUCTIVE SUBSTRATE XEROX CORPORATION (US) 1996-05-07 — — US claimed
EP-0615857-A1 Recording sheets containing monoammonium compounds XEROX CORPORATION (US) 1994-09-21 — — EP claimed
US-5320902-A Suitable for use in ink jet printing XEROX CORPORATION (US) 1994-06-14 — — US claimed
EP-0075524-B1 CARBONYLATION PROCESS OF CONJUGATED DIENES IN THE PRESENCE OF A PALLADIUM CATALYST WITH RECYCLING OF SAID CATALYST RHONE-POULENC CHIMIE DE BASE (FR) 1984-09-12 — — EP claimed
US-4454333-A DISTILLATION WITH QUATERNARY PHOSPHONIUM, ARSONIUM OR AMMONIUM RHONE-POULENC CHIMIE DE BASE (FR) 1984-06-12 — — US claimed
CN-107840347-B Titanium-silicon molecular sieve and preparation method and application thereof 中国石油化工股份有限公司 2020-08-18 — — CN disclosed
CN-107840344-B Titanium-silicon molecular sieve and preparation method and application thereof 中国石油化工股份有限公司 2020-08-18 — — CN disclosed
CN-106029658-B Method for preparing thiamethoxam 龙灯农业化工国际有限公司 2019-08-16 — — CN disclosed
CN-107840345-B A kind of application of the preparation method of silica zeolite, processing method and silica zeolite, catalyst and catalyst 中国石油化工股份有限公司 2019-07-19 — — CN disclosed
CN-107840346-B A kind of application of the preparation method of silica zeolite, processing method and silica zeolite, catalyst and catalyst 中国石油化工股份有限公司 2019-07-19 — — CN disclosed
CN-107840348-A The preparation method and mesopore molecular sieve and catalyst of a kind of mesopore molecular sieve 中国石油化工股份有限公司 2018-03-27 — — CN disclosed
CN-107840344-A A kind of HTS and its preparation method and application 中国石油化工股份有限公司 2018-03-27 — — CN disclosed
CN-107840346-A A kind of application of the preparation method of silica zeolite, processing method and silica zeolite, catalyst and catalyst 中国石油化工股份有限公司 2018-03-27 — — CN disclosed
CN-107840347-A A kind of HTS and its preparation method and application 中国石油化工股份有限公司 2018-03-27 — — CN disclosed
CN-107840345-A A kind of application of the preparation method of silica zeolite, processing method and silica zeolite, catalyst and catalyst 中国石油化工股份有限公司 2018-03-27 — — CN disclosed
WO-2015180585-A9 METHOD OF PRODUCING THIAMETHOXAM ROTAM AGROCHEM INTERNATIONAL COMPANY LIMITED (CN) 2016-12-15 — — WO disclosed
CN-106029658-A Method for preparing thiamethoxam 龙灯农业化工国际有限公司 2016-10-12 — — CN disclosed
WO-2015180585-A1 METHOD OF PRODUCING THIAMETHOXAM ROTAM AGROCHEM INTERNATIONAL COMPANY LIMITED (CN) 2015-12-03 — — WO disclosed
US-7572380-B2 Method for oxyanion removal from ground water THE PENN STATE RESEARCH FOUNDATION (US) 2009-08-11 — — US disclosed
US-20090057228-A1 SYSTEM AND METHOD OF FILTERING USING STRATIFIED ACTIVATED CARBON SIEMENS WATER TECHNOLOGIES CORP. (US) 2009-03-05 — — US disclosed
US-20080214386-A1 Stability; easily separated from solution; surface treatment of catalyst with Group seven compound; reacting epoxide with carbon dioxide NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY (JP) 2008-09-04 — — US disclosed
EP-1187833-B1 METHOD OF PRODUCING THIAMETHOXAM SYNGENTA PARTICIPATIONS AG (CH) 2007-06-06 — — EP disclosed
US-7157006-B2 Method for perchlorate removal from ground water THE PENN STATE RESEARCH FOUNDATION (US) 2007-01-02 — — US disclosed
US-20060102562-A1 Method for oxyanion removal from ground water THE PENN STATE RESEARCH FOUNDATION 2006-05-18 — — US disclosed
WO-2006047613-A2 A METHOD FOR OXYANION REMOVAL FROM GROUND WATER THE PENN STATE RESEARCH FOUNDATION (US) 2006-05-04 — — WO disclosed
US-20050167366-A1 Method for perchlorate removal from ground water THE PENN STATE RESEARCH FOUNDATION 2005-08-04 — — US disclosed
US-6881348-B2 Method for perchlorate removal from ground water THE PENN STATE RESEARCH FOUNDATION (US) 2005-04-19 — — US disclosed
US-6747146-B2 USING PHASE TRANSFER CATALYST AND QUATERNARY AMMONIUM COMPOUND SYNGENTA CROP PROTECTION, INC. 2004-06-08 — — US disclosed
US-20030092915-A1 Method of producing nitroguanidine- and nitroenamine derivatives SYNGENTA CROP PROTECTION, INC. 2003-05-15 — — US disclosed
US-20030080065-A1 Method for perchlorate removal from ground water THE PENN STATE RESEARCH FOUNDATION 2003-05-01 — — US disclosed
WO-2002100509-A1 A METHOD FOR PERCHLORATE REMOVAL FROM GROUND WATER THE PENN STATE RESEARCH FOUNDATION (US) 2002-12-19 — — WO disclosed
EP-1187833-A1 METHOD OF PRODUCING NITROGUANIDINE- AND NITROENAMINE DERIVATIVES Syngenta Participations AG (CH) 2002-03-20 — — EP disclosed
WO-2001000623-A1 METHOD OF PRODUCING NITROGUANIDINE- AND NITROENAMINE DERIVATIVES SYNGENTA PARTICIPATIONS AG (CH) 2001-01-04 — — WO disclosed
EP-0743574-B1 Migration imaging members XEROX CORP (US) 2000-12-27 — — EP disclosed
EP-0743573-B1 Method for obtaining image contrast migration imaging members XEROX CORP (US) 2000-09-06 — — EP disclosed
EP-0615857-B1 Recording sheets containing monoammonium compounds XEROX CORP (US) 1998-11-11 — — EP disclosed
EP-0736130-B1 A METHOD FOR INHIBITING THE PLUGGING OF CONDUITS BY GAS HYDRATES SHELL INT RESEARCH (NL) 1998-07-15 — — EP disclosed
US-5714270-A Multifunctional recording sheets XEROX CORPORATION (US) 1998-02-03 — — US disclosed
US-5709976-A Coated papers XEROX CORPORATION (US) 1998-01-20 — — US disclosed
US-5672424-A Ink jet transparencies XEROX CORPORATION (US) 1997-09-30 — — US disclosed
US-5648575-A Method for inhibiting the plugging of conduits by gas hydrates SHELL OIL COMPANY (US) 1997-07-15 — — US disclosed
EP-0743573-A2 Method for obtaining image contrast migration imaging members XEROX CORPORATION (US) 1996-11-20 — — EP disclosed
EP-0743574-A2 Migration imaging members XEROX CORPORATION (US) 1996-11-20 — — EP disclosed
EP-0736130-A1 A METHOD FOR INHIBITING THE PLUGGING OF CONDUITS BY GAS HYDRATES SHELL INTERNATIONALE RESEARCHMAATSCHAPPIJ B.V. (NL) 1996-10-09 — — EP disclosed
US-5563014-A SOFTENABLE LAYER CONTAINIG PHOTOSENSITIVE MARKING MATERIAL; TRANSPARENTIZING AGENT XEROX CORPORATION (US) 1996-10-08 — — US disclosed
US-5514505-A SELECTIVE TRANSPARENTIZATION OF PHOTOSENSITIVE MIGRATION MARKING PARTICLES EMBEDDED NEAR THE SURFACE OF A SOFTENABLE LAYER SUPPORTED BY AN ELECTROCONDUCTIVE SUBSTRATE XEROX CORPORATION (US) 1996-05-07 — — US disclosed
US-5460728-A Using quaternary ammonium compound as inhibitor of hydrate formation SHELL OIL COMPANY (US) 1995-10-24 — — US disclosed
WO-1995017579-A1 A METHOD FOR INHIBITING THE PLUGGING OF CONDUITS BY GAS HYDRATES SHELL INTERNATIONALE RESEARCH MAATSCHAPPIJ B.V. (NL) 1995-06-29 — — WO disclosed
EP-0615857-A1 Recording sheets containing monoammonium compounds XEROX CORPORATION (US) 1994-09-21 — — EP disclosed
US-5320902-A Suitable for use in ink jet printing XEROX CORPORATION (US) 1994-06-14 — — US disclosed
EP-0340408-B1 PROCESS FOR THE PREPARATION OF 2-HYDROXY-4-(2'-HYDROXYETHOXY)-BENZOPHENONES BASF Aktiengesellschaft (DE) 1992-12-09 — — EP disclosed
US-4885396-A REACTING 2,4-DIHYDROXYBENZOPHENONE WITH ETHYLENE CARBONATE IN PRESENCE OF QUATERNARY AMMONIUM CATALYST BASF AKTIENGESELLSCHAFT (DE) 1989-12-05 — — US disclosed
EP-0340408-A1 Process for the preparation of 2-hydroxy-4-(2'-hydroxyethoxy)-benzophenones BASF Aktiengesellschaft (DE) 1989-11-08 — — EP disclosed
EP-0159294-B1 PROCESS FOR PREPARING CYCLIC PHOSPHOROUS-ACID ESTERS CIBA-GEIGY AG (CH) 1988-11-17 — — EP disclosed
US-4692540-A Process for the preparation of cyclic phosphites CIBA-GEIGY CORPORATION (US) 1987-09-08 — — US disclosed
EP-0093363-B1 PROCESS FOR THE PREPARATION OF DISULPHIDES CASSELLA Aktiengesellschaft (DE) 1987-01-14 — — EP disclosed
EP-0159294-A2 Process for preparing cyclic phosphorous-acid esters CIBA-GEIGY AG (CH) 1985-10-23 — — EP disclosed
EP-0093362-B1 PROCESS FOR THE PREPARATION OF SULFUR DYES OF THE PHTHALOCYANINE SERIES CASSELLA Aktiengesellschaft (DE) 1985-02-20 — — EP disclosed
US-4486350-A REDUCTION OF SULFOCHLORIDE WITH REDUCING AGENT IN PRESENCE OF HYDRIODIC ACID CASSELLA AKTIENGESELLSCHAFT (DE) 1984-12-04 — — US disclosed
US-4454333-A DISTILLATION WITH QUATERNARY PHOSPHONIUM, ARSONIUM OR AMMONIUM RHONE-POULENC CHIMIE DE BASE (FR) 1984-06-12 — — US disclosed
EP-0093363-A1 Process for the preparation of disulphides CASSELLA Aktiengesellschaft (DE) 1983-11-09 — — EP disclosed
EP-0093363-A1 Process for the preparation of disulphides CASSELLA Aktiengesellschaft (DE) 1983-11-09 — — EP disclosed
EP-0093362-A1 Process for the preparation of sulfur dyes of the phthalocyanine series CASSELLA Aktiengesellschaft (DE) 1983-11-09 — — 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 (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-20030092915-A1 Method of producing nitroguanidine- and nitroenamine derivatives CBR1, CBR3, NOX1 ALDH1A1 1306/4885TP53 4701/4885CYP3A4 301/4885

“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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