Bromide

Bromide

SCHEMBL6428595

[Br-].c1ccc([P+](CC2CCC2)(c2ccccc2)c2ccccc2)cc1

nearest known ligand 0.44

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 14)

geneUniProtsupporting neighboursconfidence
OPRM1 known ✓ P35372 1/20 0.38
HIF1A Q16665 2/20 0.44
OPRD1 P41143 1/20 0.38
OPRK1 P41145 1/20 0.38
CYP1A2 P05177 2/20 0.36
CYP2D6 P10635 2/20 0.36
ALDH1A1 P00352 1/20 0.35
TSHR P16473 1/20 0.35
CYP2C19 P33261 1/20 0.35
SNCA P37840 1/20 0.35
MMP2 P08253 1/20 0.35
MMP9 P14780 1/20 0.35
MMP12 P39900 1/20 0.35
SLC18A2 Q05940 1/20 0.34

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 SCHEMBL1582234 0.94 HIF1A (0.43) HIF1AALDH1A1TSHRMMP2MMP9
Iodide SCHEMBL1969660 0.92 HIF1A (0.44) HIF1AOPRM1OPRD1OPRK1CYP1A2
Bromide SCHEMBL129506 0.91 HIF1A (0.48) HIF1ACYP1A2CYP2D6ALDH1A1TSHR
Hydrochloric Acid SCHEMBL5234960 0.90 HIF1A (0.43) HIF1ATSHRMMP2MMP9MMP12
Iodide SCHEMBL13280558 0.87 HIF1A (0.48) HIF1ACYP1A2CYP2D6ALDH1A1TSHR
Bromide SCHEMBL28548705 0.82 HIF1A (0.40) HIF1ACYP1A2CYP2D6ALDH1A1TSHR
SCHEMBL8379392 0.82 HIF1A (0.43) HIF1ACYP1A2CYP2D6ALDH1A1TSHR
SCHEMBL8373290 0.82 HIF1A (0.43) HIF1ACYP1A2CYP2D6ALDH1A1TSHR
Bromide SCHEMBL7559700 0.80 HIF1A (0.38) HIF1AOPRM1OPRK1ALDH1A1
Bromide SCHEMBL7559694 0.80 HIF1A (0.38) HIF1AOPRM1OPRK1ALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2025077841-A1 AMIDE-SUBSTITUTED CYCLOALKYL COMPOUNDS, PREPARATION METHOD THEREFOR AND MEDICAL USES THEREOF 江苏恒瑞医药股份有限公司 2025-04-17 WO disclosed
US-6897306-B2 3-heterocyclylpropanohydroxamic acids PFIZER PRODUCTS, INC. (US) 2005-05-24 US disclosed
EP-1240152-B1 OX(ADI)AZOLYL-HYDROXAMIC ACIDS USEFUL AS PROCOLLAGEN C-PROTEINASE INHIBITORS PFIZER LTD (GB) 2004-12-08 EP disclosed
US-20030119807-A1 3-Heterocyclylpropanohydroxamic acids BAILEY SIMON (US) 2003-06-26 US disclosed
EP-1240152-A1 OX(ADI)AZOLYL-HYDROXAMIC ACIDS USEFUL AS PROCOLLAGEN C-PROTEINASE INHIBITORS Pfizer Limited (GB) 2002-09-18 EP disclosed
US-6448278-B2 ANTISCARRING AGENT PFIZER INC. 2002-09-10 US disclosed
US-20010021718-A1 Procollagen C-proteinase inhibitors PFIZER INC. 2001-09-13 US disclosed
WO-2001047901-A1 OX(ADI)AZOLYL-HYDROXAMIC ACIDS USEFUL AS PROCOLLAGEN C-PROTEINASE INHIBITORS PFIZER LIMITED (GB) 2001-07-05 WO 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-20010021718-A1 Procollagen C-proteinase inhibitors MMP1, CTSL, PREP OPRM1 3643/4885HIF1A 2165/4885OPRD1 4100/4885
US-20030119807-A1 3-Heterocyclylpropanohydroxamic acids CPA1, MMP1, PREP OPRM1 3333/4885HIF1A 715/4885OPRD1 3120/4885

“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.