Bromide

Bromide

SCHEMBL3558232

COC(=O)c1ccccc1C[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 16)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 3/20 0.53
LMNA P02545 2/20 0.53
HIF1A Q16665 1/20 0.48
TSHR P16473 2/20 0.46
HSD17B10 Q99714 2/20 0.45
CFTR P13569 1/20 0.45
MAPT P10636 1/20 0.44
ALOX15 P16050 1/20 0.44
KMT2A Q03164 1/20 0.44
KDM4E B2RXH2 2/20 0.44
POLB P06746 2/20 0.44
ATM Q13315 1/20 0.44
SLC6A3 Q01959 1/20 0.43
TSPO P30536 2/20 0.42
GLA P06280 1/20 0.42
HTT P42858 1/20 0.42

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 SCHEMBL29627822 0.87 PTGDR2 (0.44) ALDH1A1LMNAHIF1ATSHRHSD17B10
SCHEMBL29627816 0.85 PTGDR2 (0.45) ALDH1A1LMNAHIF1ATSHRHSD17B10
Bromide SCHEMBL3918746 0.85 TSHR (0.57) ALDH1A1TSHRHSD17B10KMT2AKDM4E
Bromide SCHEMBL11599708 0.84 KDM4E (0.49) ALDH1A1LMNATSHRHSD17B10MAPT
Bromide SCHEMBL17714307 0.83 ABL1 (0.48) ALDH1A1LMNAHSD17B10KMT2AKDM4E
Bromide SCHEMBL17714327 0.83 PLA2G2A (0.46) ALDH1A1LMNATSHRMAPTKDM4E
Bromide SCHEMBL7841361 0.83 ALDH1A1 (0.45) ALDH1A1LMNAHIF1AHSD17B10KMT2A
Bromide SCHEMBL4509169 0.83 ALDH1A1 (0.48) ALDH1A1LMNATSHRHSD17B10KMT2A
Bromide SCHEMBL31123663 0.81 DPP4 (0.42) ALDH1A1LMNATSHRHSD17B10CFTR
Bromide SCHEMBL10635701 0.81 ALDH1A1 (0.56) ALDH1A1LMNATSHRMAPTKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4692092-A1 NOVEL COMPOUNDS WITH MTORC2-INHIBITORY ACTIVITY AND USES THEREOF Aliad Biopharma (KR) 2026-02-11 EP disclosed
WO-2024205377-A1 NOVEL COMPOUNDS WITH MTORC2-INHIBITORY ACTIVITY AND USES THEREOF 알리아드바이오파마 주식회사 2024-10-03 WO disclosed
US-7816397-B2 Phenylcarboxylic acid derivatives and use thereof for the treatment of diabetes MERCK PATENT GMBH (DE) 2010-10-19 US disclosed
US-20090105327-A1 Dibenzocycloheptane compounds and pharmaceuticals containing these compounds MERCKLE GMBH (DE) 2009-04-23 US disclosed
US-20080045483-A1 Phenylcarboxylic Acid Derivatives and Use Thereof for the Treatment of Diabetes MERCK PATENT GMBH (DE) 2008-02-21 US disclosed
EP-1881968-A2 DIBENZOCYCLOHEPTANE COMPOUNDS AND PHARMACEUTICALS CONTAINING THESE COMPOUNDS MERCKLE GMBH (DE) 2008-01-30 EP disclosed
US-7309718-B2 Dibenzocycloheptene compound UBE INDUSTRIES, LTD. (JP) 2007-12-18 US disclosed
EP-1761486-A1 PHENYLCARBOXYLIC ACID DERIVATIVES AND USE THEREOF FOR THE TREATMENT OF DIABETES Merck Patent GmbH (DE) 2007-03-14 EP disclosed
WO-2006120010-A2 DIBENZOCYCLOHEPTANE COMPOUNDS AND PHARMACEUTICALS CONTAINING THESE COMPOUNDS MERCKLE GMBH (DE) 2006-11-16 WO disclosed
WO-2006000288-A1 PHENYLCARBOXYLIC ACID DERIVATIVES AND USE THEREOF FOR THE TREATMENT OF DIABETES MERCK PATENT GMBH (DE) 2006-01-05 WO disclosed
US-4882351-A CARDIOVASCULAR DISORDERS; ROUSSEL UCLAF (FR) 1989-11-21 US disclosed
EP-0312051-A2 Tricyclic compounds KYOWA HAKKO KOGYO CO., LTD. (JP) 1989-04-19 EP disclosed
EP-0303512-A1 Substituted dibenzocycloheptenimines MERCK SHARP & DOHME LTD. (GB) 1989-02-15 EP disclosed
US-4782085-A LIPOXYGENASE INHIBITORS E. R. SQUIBB & SONS, INC. (US) 1988-11-01 US disclosed
US-4711900-A LIPOXYGENASE INHIBITORS E. R. SQUIBB & SONS, INC. (US) 1987-12-08 US disclosed
EP-0244077-A1 Sulphides derived from substituted phenyl-2-acrylic acid IMPERIAL CHEMICAL INDUSTRIES PLC (GB) 1987-11-04 EP disclosed
US-4474804-A 7-Oxabicyclo substituted prostaglandin phenyl carboxylic acid derivatives useful as cardiovascular agents E. R. SQUIBB & SONS, INC. (US) 1984-10-02 US disclosed
US-4054579-A Intermediates in the process for the preparation of 2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)acetic, propionic and butyric acids SYNTEX (U.S.A.) INC. (US) 1977-10-18 US disclosed
US-4011243-A Intermediate in the oxidative process for the preparation of 2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)acetic, propionic and butyric acids SYNTEX (U.S.A.) INC. (US) 1977-03-08 US disclosed
US-3979430-A Solvolytic process for the preparation of 2-(5H-dibenzo[a,d]cyclohepten-5-on-2-yl)acetic, propionic and butyric acids SYNTEX (U.S.A.) INC. (US) 1976-09-07 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 (2 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-20080045483-A1 Phenylcarboxylic Acid Derivatives and Use Thereof for the Treatment of Diabetes SLC5A1, ALDH7A1, ASS1 ALDH1A1 61/4885LMNA 2120/4885HIF1A 353/4885
US-20090105327-A1 Dibenzocycloheptane compounds and pharmaceuticals containing these compounds BDKRB1, IL1R1, IL1A ALDH1A1 420/4885LMNA 4294/4885HIF1A 517/4885

“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.