Bromide

Bromide

SCHEMBL1016601

Br.O=C(CBr)c1ccccn1

nearest known ligand 0.57

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 17)

geneUniProtsupporting neighboursconfidence
CES2 O00748 1/20 0.57
CES1 P23141 1/20 0.57
GRM4 Q14833 1/20 0.56
L3MBTL1 Q9Y468 4/20 0.55
LMNA P02545 1/20 0.55
NAPRT Q6XQN6 1/20 0.55
P4HTM Q9NXG6 1/20 0.55
ALDH1A1 P00352 2/20 0.53
GSK3B P49841 2/20 0.53
CTNNB1 P35222 5/20 0.51
WNT3A P56704 4/20 0.51
KMT2A Q03164 2/20 0.50
PTPN1 P18031 1/20 0.47
KDM4E B2RXH2 1/20 0.46
GAA P10253 1/20 0.46
SMN1; SMN2 Q16637 1/20 0.45
TLR7 Q9NYK1 1/20 0.44

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 SCHEMBL29601697 1.00 CES2 (0.57) CES2CES1GRM4L3MBTL1LMNA
SCHEMBL29601127 0.98 CES2 (0.59) CES2CES1GRM4L3MBTL1LMNA
SCHEMBL504833 0.98 CES2 (0.59) CES2CES1GRM4L3MBTL1LMNA
Hydrochloric Acid SCHEMBL6833226 0.96 CES2 (0.57) CES2CES1GRM4L3MBTL1LMNA
Bromide SCHEMBL5121089 0.94 CES2 (0.55) CES2CES1GRM4L3MBTL1LMNA
Pyridine SCHEMBL8599632 0.91 L3MBTL1 (0.55) CES2CES1GRM4L3MBTL1LMNA
SCHEMBL12777709 0.82 CES2 (0.59) CES2CES1GRM4L3MBTL1LMNA
SCHEMBL2470002 0.81 CTNNB1 (0.71) CES2CES1GRM4L3MBTL1LMNA
SCHEMBL253276 0.81 CES2 (0.64) CES2CES1GRM4L3MBTL1LMNA
SCHEMBL29355245 0.81 CES2 (0.64) CES2CES1GRM4L3MBTL1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230219976-A1 AMORPHOUS SOLID FORM OF A BET PROTEIN INHIBITOR INCYTE CORPORATION 2023-07-13 US claimed
US-10858372-B2 Amorphous solid form of a BET protein inhibitor INCYTE CORPORATION (US) 2020-12-08 US claimed
US-20190300545-A1 AMORPHOUS SOLID FORM OF A BET PROTEIN INHIBITOR INCYTE CORPORATION 2019-10-03 US claimed
US-10329305-B2 Amorphous solid form of a BET protein inhibitor INCYTE CORPORATION (US) 2019-06-25 US claimed
US-20180273546-A1 AMORPHOUS SOLID FORM OF A BET PROTEIN INHIBITOR INCYTE CORPORATION 2018-09-27 US claimed
US-20170121347-A1 AMORPHOUS SOLID FORM OF A BET PROTEIN INHIBITOR INCYTE CORPORATION 2017-05-04 US claimed
WO-2017075377-A1 AMORPHOUS SOLID FORM OF A BET PROTEIN INHIBITOR INCYTE CORPORATION (US) 2017-05-04 WO claimed
US-20250388582-A1 NOVEL BICYCLIC HETEROARYL COMPOUND AND USE THEREOF ILDONG PHARMACEUTICAL CO LTD (KR) 2025-12-25 US disclosed
EP-4626896-A1 POLYELECTROPHILIC METALATED HETEROCYCLES DERIVED FROM 2-(PYRIDIN-2-YL)IMIDAZO[1,2-A]PYRIDINE AND USE THEREOF AS CHEMOTHERAPEUTIC AGENTS Universidad del País Vasco/Euskal Herriko Unibertsitatea (ES) 2025-10-08 EP disclosed
US-20250229198-A1 COMPOUNDS FOR SEPARATION OF RARE EARTH ELEMENTS AND S-, P-, D- METALS, METHOD OF SEPARATION, AND USE THEREOF USTAV ORGANICKE CHEMIE A BIOCHEMIE AV CR, V.V.I (CZ) 2025-07-17 US disclosed
EP-4585599-A1 NITROGEN-CONTAINING FUSED RING COMPOUND, INTERMEDIATE THEREOF, PREPARATION METHOD THEREFOR AND USE THEREOF Hangzhou Synrx Therapeutics Biomedical Technology Co., Ltd. (CN) 2025-07-16 EP disclosed
EP-4556476-A1 NOVEL BICYCLIC HETEROARYL COMPOUND AND USE THEREOF Ildong Pharmaceutical Co., Ltd. (KR) 2025-05-21 EP disclosed
US-12268977-B2 Compounds for separation of rare earth elements and s-, p-, d-metals, method of separation, and use thereof USTAV ORGANICKE CHEMIE A BIOCHEMIE AV CR. V.V.I. (CZ) 2025-04-08 US disclosed
EP-0555480-A1 NOVEL THIAZOLE DERIVATIVE YAMANOUCHI PHARMACEUTICAL CO. LTD. (JP) 1993-08-18 EP disclosed
US-5026702-A Enhances physical performance in animals, effective in lowering blood sugar, reducing body fat and lowering atherogenic lipoproteins DR. KARL THOMAE, GMBH (DE) 1991-06-25 US disclosed
EP-0372125-A1 Oxazole and thiazole derivatives AKZO N.V. (NL) 1990-06-13 EP disclosed
EP-0368384-A1 Thiazole derivatives AKZO N.V. (NL) 1990-05-16 EP disclosed
EP-0334146-A1 Morpholines and morpholine-N-oxides, medicines containing these compounds and process for their preparation Dr. Karl Thomae GmbH (DE) 1989-09-27 EP disclosed
US-4492695-A ANTICONVULSANTS, SEDATIVES, TRANQUILIZERS SYNTHELABO (FR) 1985-01-08 US disclosed
US-4005212-A ANTIDEPRESSANT, ANOREXIGENIC, PSYCHOENERGIZING, 2-PHENYL-2,3,5,6-TETRAHYDROIMIDAZO(2,1-B)THIAZOLE RHONE-POULENC S.A. (FR) 1977-01-25 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 (9 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-20170121347-A1 AMORPHOUS SOLID FORM OF A BET PROTEIN INHIBITOR BRD1, BRD3, BRD2 CES2 4856/4885CES1 4060/4885GRM4 3852/4885
US-10329305-B2 Amorphous solid form of a BET protein inhibitor BRD1, BRD3, BRD2 CES2 4856/4885CES1 4060/4885GRM4 3852/4885
US-20230219976-A1 AMORPHOUS SOLID FORM OF A BET PROTEIN INHIBITOR BRD1, BRD3, BRD2 CES2 4856/4885CES1 4060/4885GRM4 3852/4885
US-20180273546-A1 AMORPHOUS SOLID FORM OF A BET PROTEIN INHIBITOR BRD1, BRD3, BRD2 CES2 4854/4885CES1 4068/4885GRM4 3507/4885
US-20190300545-A1 AMORPHOUS SOLID FORM OF A BET PROTEIN INHIBITOR BRD1, BRD3, BRD2 CES2 4856/4885CES1 4060/4885GRM4 3852/4885
US-20250229198-A1 COMPOUNDS FOR SEPARATION OF RARE EARTH ELEMENTS AND S-, P-, D- METALS, METHOD OF SEPARATION, AND USE THEREOF SCO2, SOD3, SLC39A3 CES2 2023/4885CES1 3686/4885GRM4 3674/4885
US-20250388582-A1 NOVEL BICYCLIC HETEROARYL COMPOUND AND USE THEREOF GBA1, PIKFYVE, MAN2B1 CES2 1314/4885CES1 108/4885GRM4 4718/4885
US-10858372-B2 Amorphous solid form of a BET protein inhibitor BRD1, BRD3, BRD2 CES2 4856/4885CES1 4060/4885GRM4 3852/4885
US-12268977-B2 Compounds for separation of rare earth elements and s-, p-, d-metals, method of separation, and use thereof SCLY, SFXN1, PTCD3 CES2 4075/4885CES1 3584/4885GRM4 3616/4885

“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.