Bromide

Bromide

SCHEMBL28376133

Br.c1ccc(-c2cccc(-c3ccccc3)c2)cc1

nearest known ligand 0.64

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 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 1/20 0.64
MAOA P21397 1/20 0.60
KMO O15229 1/20 0.56
MEN1 O00255 1/20 0.55
ESR1 P03372 1/20 0.55
KMT2A Q03164 1/20 0.55
MGLL Q99685 2/20 0.52
ALOX5 P09917 1/20 0.50
HDAC4 P56524 1/20 0.50
HDAC2 Q92769 1/20 0.50
HDAC8 Q9BY41 1/20 0.50
ACMSD Q8TDX5 1/20 0.48
GP6 Q9HCN6 1/20 0.48
PRSS1 P07477 1/20 0.48
PRSS2 P07478 1/20 0.48
PRSS3 P35030 1/20 0.48
CYP3A4 P08684 1/20 0.48
CYP2C9 P11712 1/20 0.48
HSD17B1 P14061 1/20 0.48
HSD17B2 P37059 1/20 0.48

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
SCHEMBL2731883 0.96 ALDH1A1 (0.69) ALDH1A1MAOAKMOMEN1ESR1
SCHEMBL31734209 0.96 ALDH1A1 (0.69) ALDH1A1MAOAKMOMEN1ESR1
SCHEMBL29354148 0.96 ALDH1A1 (0.69) ALDH1A1MAOAKMOMEN1ESR1
Biphenyl SCHEMBL11687528 0.96 ALDH1A1 (0.69) ALDH1A1MAOAKMOMEN1ESR1
SCHEMBL51426 0.96 ALDH1A1 (0.69) ALDH1A1MAOAKMOMEN1ESR1
SCHEMBL2401076 0.96 ALDH1A1 (0.69) ALDH1A1MAOAKMOMEN1ESR1
SCHEMBL6918022 0.96 ALDH1A1 (0.69) ALDH1A1MAOAKMOMEN1ESR1
SCHEMBL14481975 0.93 ALDH1A1 (0.64) ALDH1A1MAOAKMOMEN1ESR1
SCHEMBL31254135 0.93 ALDH1A1 (0.64) ALDH1A1MAOAKMOMEN1ESR1
SCHEMBL22113250 0.93 ALDH1A1 (0.64) ALDH1A1MAOAKMOMEN1ESR1

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-12297311-B2 Biaryl hydroxythiophene group IV transition metal polymerization with chain transfer capability DOW GLOBAL TECHNOLOGIES LLC (US) 2025-05-13 US disclosed
EP-3642250-B1 BIARYL PHENOXY GROUP IV TRANSITION METAL CATALYSTS FOR OLEFIN POLYMERIZATION DOW GLOBAL TECHNOLOGIES LLC (US) 2024-12-18 EP disclosed
US-12122862-B2 Biaryl hydroxythiophene group IV transition metal polymerization catalysts with chain transfer capability DOW GLOBAL TECHNOLOGIES LLC (US) 2024-10-22 US disclosed
US-20220169756-A1 BIARYL HYDROXYTHIOPHENE GROUP IV TRANSITION METAL POLYMERIZATION WITH CHAIN TRANSFER CAPABILITY DOW GLOBAL TECHNOLOGIES LLC (US) 2022-06-02 US disclosed
CN-110809586-A Biarylphenoxy group IV transition metal catalysts for olefin polymerization 陶氏环球技术有限责任公司 2020-02-18 CN 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-12122862-B2 Biaryl hydroxythiophene group IV transition metal polymerization catalysts with chain transfer capability TRMT1, GFPT1, BCAT1 ALDH1A1 421/4885MAOA 914/4885KMO 355/4885

“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.