Bromide

Bromide

SCHEMBL1944264

Br.Cc1cccc2c(=O)[nH]c(CCN3CCC[C@@H]3CO)cc12

nearest known ligand 0.98

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
HTR1D known ✓ P28221 1/20 0.39
HTR1B known ✓ P28222 1/20 0.39
PARP1 P09874 3/20 0.98
CCNE2 O96020 1/20 0.43
CDK4 P11802 1/20 0.43
PRKACA P17612 1/20 0.43
PRKACG P22612 1/20 0.43
PRKACB P22694 1/20 0.43
CCND1 P24385 1/20 0.43
CCNE1 P24864 1/20 0.43
CDK2 P24941 1/20 0.43
CAMK2B Q13554 1/20 0.43
CAMK2G Q13555 1/20 0.43
CAMK2D Q13557 1/20 0.43
CAMK2A Q9UQM7 1/20 0.43
SPHK2 Q9NRA0 2/20 0.42
SPHK1 Q9NYA1 2/20 0.42
HRH3 Q9Y5N1 2/20 0.41
TNKS O95271 6/20 0.39
KDM4E B2RXH2 2/20 0.39

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 SCHEMBL1944266 1.00 PARP1 (0.98) PARP1CCNE2CDK4PRKACAPRKACG
Bromide SCHEMBL1946605 0.99 PARP1 (0.96) PARP1CCNE2CDK4PRKACAPRKACG
Bromide SCHEMBL1946607 0.99 PARP1 (0.96) PARP1CCNE2CDK4PRKACAPRKACG
SCHEMBL1946020 0.99 PARP1 (1.00) PARP1CCNE2CDK4PRKACAPRKACG
SCHEMBL30417469 0.99 PARP1 (1.00) PARP1CCNE2CDK4PRKACAPRKACG
SCHEMBL1945766 0.99 PARP1 (1.00) PARP1CCNE2CDK4PRKACAPRKACG
SCHEMBL30090665 0.99 PARP1 (1.00) PARP1CCNE2CDK4PRKACAPRKACG
SCHEMBL3443321 0.99 PARP1 (1.00) PARP1CCNE2CDK4PRKACAPRKACG
Hydrochloric Acid SCHEMBL1946669 0.98 PARP1 (0.98) PARP1CCNE2CDK4PRKACAPRKACG
Hydrochloric Acid SCHEMBL1946668 0.98 PARP1 (0.98) PARP1CCNE2CDK4PRKACAPRKACG

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
EP-2184282-A1 NOVEL SALT OF ISOQUINOLINE COMPOUND AND CRYSTAL THEREOF Mitsubishi Tanabe Pharma Corporation (JP) 2010-05-12 EP claimed
EP-2184282-B1 NOVEL SALT OF ISOQUINOLINE COMPOUND AND CRYSTAL THEREOF MITSUBISHI TANABE PHARMA CORP (JP) 2014-10-08 EP disclosed
US-8309573-B2 Salt of isoquinoline compound and crystal thereof MITSUBISHI TANABE PHARMA CORPORATION (JP) 2012-11-13 US disclosed
US-20110130419-A1 NOVEL SALT OF ISOQUINOLINE COMPOUND AND CRYSTAL THEREOF MITSUBISHI TANABE PHARMA CORPORATION (JP) 2011-06-02 US disclosed
EP-2184282-A1 NOVEL SALT OF ISOQUINOLINE COMPOUND AND CRYSTAL THEREOF Mitsubishi Tanabe Pharma Corporation (JP) 2010-05-12 EP 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-20110130419-A1 NOVEL SALT OF ISOQUINOLINE COMPOUND AND CRYSTAL THEREOF IMPDH1, IMPDH2, MTAP HTR1D 372/4885HTR1B 392/4885PARP1 415/4885

“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.