Bromide

Bromide

SCHEMBL17822672

Br.c1ccc(CN[C@H]2CCCC[C@@H]2NCc2ccccc2)cc1.c1ccc(CN[C@H]2CCCC[C@@H]2NCc2ccccc2)cc1

nearest known ligand 0.56

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 15)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 2/20 0.47
KDM1A O60341 7/20 0.56
MAOA P21397 4/20 0.56
GRIN2B Q13224 2/20 0.52
FUCA1 P04066 1/20 0.49
SSTR3 P32745 3/20 0.48
BCHE P06276 2/20 0.47
BACE1 P56817 2/20 0.47
MEN1 O00255 1/20 0.47
RAB9A P51151 1/20 0.47
KMT2A Q03164 1/20 0.47
HRH3 Q9Y5N1 1/20 0.46
MAOB P27338 3/20 0.45
EPHX1 P07099 1/20 0.45
HPGD P15428 1/20 0.45

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 SCHEMBL16799767 1.00 KDM1A (0.56) KDM1AMAOAGRIN2BFUCA1SSTR3
Bromide SCHEMBL17822691 1.00 KDM1A (0.56) KDM1AMAOAGRIN2BFUCA1SSTR3
Bromide SCHEMBL19876392 1.00 KDM1A (0.56) KDM1AMAOAGRIN2BFUCA1SSTR3
Bromide SCHEMBL18106675 1.00 KDM1A (0.56) KDM1AMAOAGRIN2BFUCA1SSTR3
Bromide SCHEMBL18129441 1.00 KDM1A (0.56) KDM1AMAOAGRIN2BFUCA1SSTR3
Bromide SCHEMBL17822680 1.00 KDM1A (0.56) KDM1AMAOAGRIN2BFUCA1SSTR3
SCHEMBL2198525 0.98 KDM1A (0.58) KDM1AMAOAGRIN2BFUCA1SSTR3
SCHEMBL2197651 0.98 KDM1A (0.58) KDM1AMAOAGRIN2BFUCA1SSTR3
SCHEMBL2798417 0.98 KDM1A (0.58) KDM1AMAOAGRIN2BFUCA1SSTR3
SCHEMBL491107 0.98 KDM1A (0.58) KDM1AMAOAGRIN2BFUCA1SSTR3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10464891-B2 Urea derivative or pharmacologically acceptable salt thereof KYORIN PHARMACEUTICALS CO., LTD. (JP) 2019-11-05 US disclosed
EP-3230264-B1 3-OXO-3-(ARYLAMINO)PROPANOATES, A PROCESS FOR THEIR PREPARATION, AND THEIR USE IN PREPARING PYRROLIDINONES FMC CORP (US) 2019-09-11 EP disclosed
US-10227286-B2 3-oxo-3-(arylamino)propanoates, a process for their preparation, and their use in preparing pyrrolidinones FMC CORPORATION (US) 2019-03-12 US disclosed
EP-3075726-B1 UREA DERIVATIVES OR PHARMACOLOGICALLY ACCEPTABLE SALTS THEREOF USEFUL AS FORMYL PEPTIDE RECEPTOR LIKE 1 (FPRL-1) AGONISTS KYORIN SEIYAKU KK (JP) 2017-11-08 EP disclosed
EP-3230264-A1 3-OXO-3-(ARYLAMINO)PROPANOATES, A PROCESS FOR THEIR PREPARATION, AND THEIR USE IN PREPARING PYRROLIDINONES E. I. du Pont de Nemours and Company (US) 2017-10-18 EP disclosed
EP-3075726-A1 UREA DERIVATIVE OR PHARMACOLOGICALLY ACCEPTABLE SALT THEREOF Kyorin Pharmaceutical Co., Ltd. (JP) 2016-10-05 EP disclosed
WO-2016094117-A1 3-OXO-3-(ARYLAMINO)PROPANOATES, A PROCESS FOR THEIR PREPARATION, AND THEIR USE IN PREPARING PYRROLIDINONES E. I. DU PONT DE NEMOURS AND COMPANY (US) 2016-06-16 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-10227286-B2 3-oxo-3-(arylamino)propanoates, a process for their preparation, and their use in preparing pyrrolidinones SDHA, SDHB, NDUFV3 ACHE 1886/4885KDM1A 898/4885MAOA 246/4885
US-10464891-B2 Urea derivative or pharmacologically acceptable salt thereof FPR1, FPR2, FPR3 ACHE 4545/4885KDM1A 4486/4885MAOA 2343/4885

“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.