Bromide

Bromide

SCHEMBL26618263

CCCCCCCCCCCCCCCCCC(=O)[N+](CC)(CC)C(=O)CCCCCCCCCCCCCCCCC.[Br-]

nearest known ligand 0.52

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 20)

geneUniProtsupporting neighboursconfidence
CES2 O00748 4/20 0.52
CES1 P23141 4/20 0.52
GPR84 Q9NQS5 7/20 0.50
PPARG P37231 7/20 0.50
PPARD Q03181 7/20 0.50
PPARA Q07869 7/20 0.50
HDAC11 Q96DB2 5/20 0.50
TSHR P16473 5/20 0.50
PTPN1 P18031 3/20 0.50
ALDH1A1 P00352 3/20 0.50
TLR2 O60603 2/20 0.50
TDP1 Q9NUW8 2/20 0.50
FABP4 P15090 2/20 0.50
SLC22A6 Q4U2R8 1/20 0.50
SLC22A8 Q8TCC7 1/20 0.50
MEN1 O00255 1/20 0.50
ESR1 P03372 1/20 0.50
ALOX15 P16050 1/20 0.50
PDE4A P27815 1/20 0.50
KMT2A Q03164 1/20 0.50

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
Hydrochloric Acid SCHEMBL28951891 0.95 CES2 (0.52) CES2CES1GPR84PPARGPPARD
SCHEMBL5907427 0.87 CES2 (0.48) CES2CES1GPR84PPARGPPARD
SCHEMBL10524282 0.86 FABP3 (0.62) PPARGPPARDPPARAPTPN1TDP1
Hydrochloric Acid SCHEMBL9705852 0.85 FABP3 (0.61) PPARGPPARDPPARAPTPN1TDP1
SCHEMBL455072 0.84 CES2 (0.45) CES2CES1GPR84PPARGPPARD
SCHEMBL457603 0.84 CES2 (0.45) CES2CES1GPR84PPARGPPARD
Hydrochloric Acid SCHEMBL16538158 0.82 CES2 (0.43) CES2CES1GPR84PPARGPPARD
Bromide SCHEMBL11380808 0.81 CES2 (0.56) CES2CES1GPR84PPARGPPARD
Hydrochloric Acid SCHEMBL28933231 0.81 CES2 (0.42) CES2CES1GPR84PPARGPPARD
SCHEMBL28344407 0.81 MAPT (0.46) CES2CES1GPR84PPARGPPARD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250319035-A1 CATIONIC LIPID NANOPARTICLE HAVING HIGH TRANSFECTION EFFICIENCY AND PREPARATION METHOD THEREFOR TONG, Shuwen (CN) 2025-10-16 US disclosed
CN-119913209-A Composition for delivering nucleic acid into cells 苏州多纳医药科技有限公司 2025-05-02 CN disclosed
CN-119896747-A Calcium-containing lipid nanoparticle loaded with transthyretin nucleic acid for reducing transthyretin 苏州多纳医药科技有限公司 2025-04-29 CN disclosed
CN-119365189-A Cationic lipid nanoparticle with high transfection efficiency and preparation method thereof 北京多纳医药科技有限公司 2025-01-24 CN disclosed
WO-2023208076-A1 CATIONIC LIPID NANOPARTICLE HAVING HIGH TRANSFECTION EFFICIENCY AND PREPARATION METHOD THEREFOR 北京多纳医药科技有限公司 2023-11-02 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 (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-20250319035-A1 CATIONIC LIPID NANOPARTICLE HAVING HIGH TRANSFECTION EFFICIENCY AND PREPARATION METHOD THEREFOR CETP, NPC1L1, LIPA CES2 945/4885CES1 78/4885GPR84 3916/4885

“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.