Bromide

Bromide

SCHEMBL15901554

Br.Cc1cccc(-c2ccccc2)n1

nearest known ligand 0.65

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
RAB9A P51151 5/20 0.65
KMT2A Q03164 5/20 0.65
MEN1 O00255 4/20 0.65
CCR1 P32246 1/20 0.65
CCR8 P51685 1/20 0.65
CYP2A6 P11509 1/20 0.60
TGFBR1 P36897 1/20 0.54
ASIC3 Q9UHC3 1/20 0.54
NPC1 O15118 3/20 0.47
ATM Q13315 1/20 0.47
METAP2 P50579 1/20 0.46
ALDH1A1 P00352 5/20 0.44
ADORA1 P30542 2/20 0.43
ADORA2A P29274 1/20 0.43
KDM4E B2RXH2 3/20 0.43
PKM P14618 3/20 0.43
HPGD P15428 2/20 0.43
TSHR P16473 2/20 0.43
SMN1; SMN2 Q16637 2/20 0.43
TP53 P04637 1/20 0.43

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
SCHEMBL647992 0.98 MEN1 (0.68) RAB9AKMT2AMEN1CCR1CCR8
SCHEMBL29963679 0.98 MEN1 (0.68) RAB9AKMT2AMEN1CCR1CCR8
SCHEMBL12594495 0.95 MEN1 (0.64) RAB9AKMT2AMEN1CCR1CCR8
SCHEMBL2189142 0.93 KMT2A (0.62) RAB9AKMT2AMEN1CCR1CCR8
SCHEMBL3422361 0.88 CCR1 (0.75) RAB9AKMT2AMEN1CCR1CCR8
SCHEMBL16189026 0.88 MEN1 (0.56) RAB9AKMT2AMEN1CCR1CCR8
SCHEMBL16189330 0.86 MEN1 (0.54) RAB9AKMT2AMEN1CCR1CCR8
SCHEMBL16189443 0.86 MEN1 (0.54) RAB9AKMT2AMEN1CCR1CCR8
SCHEMBL17932287 0.86 MEN1 (0.54) RAB9AKMT2AMEN1CCR1CCR8
SCHEMBL19009229 0.85 CCR1 (0.58) RAB9AKMT2AMEN1CCR1CCR8

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2762467-B1 Method for producing an optically active 2-arylpiperidinium salt TAKASAGO PERFUMERY CO LTD (JP) 2016-08-03 EP disclosed
US-9012649-B2 Method for producing optically active 2-arylpiperidinium salt TAKASAGO INTERNATIONAL CORPORATION (JP) 2015-04-21 US disclosed
EP-2762467-A1 Method for producing an optically active 2-arylpiperidinium salt Takasago International Corporation (JP) 2014-08-06 EP disclosed
US-20140213792-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE 2-ARYLPIPERIDINIUM SALT TAKASAGO INTERNATIONAL CORPORATION (JP) 2014-07-31 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 (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-20140213792-A1 METHOD FOR PRODUCING OPTICALLY ACTIVE 2-ARYLPIPERIDINIUM SALT REN, KCNH3, KCNH2 RAB9A 284/4885KMT2A 2054/4885MEN1 3297/4885

“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.