Bromide

Bromide

SCHEMBL1306423

Br.Br.Br.C1CCN(CCCN[C@H]2CCNC2)C1

nearest known ligand 0.45

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
SIGMAR1 known ✓ Q99720 1/20 0.34
RAD52 P43351 2/20 0.45
KCNH2 Q12809 1/20 0.44
LMNA P02545 1/20 0.44
SMN1; SMN2 Q16637 1/20 0.44
DPP4 P27487 1/20 0.41
FAP Q12884 1/20 0.41
DPP8 Q6V1X1 1/20 0.41
DPP9 Q86TI2 1/20 0.41
GNAI3 P08754 5/20 0.40
GNAO1 P09471 5/20 0.40
GNAI1 P63096 5/20 0.40
CXCR4 P61073 3/20 0.36
HRH3 Q9Y5N1 2/20 0.36
CYP2C9 P11712 1/20 0.36
TP53 P04637 1/20 0.33
CYP1A2 P05177 1/20 0.33
CYP3A4 P08684 1/20 0.33
CYP2D6 P10635 1/20 0.33
TSHR P16473 1/20 0.33

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
SCHEMBL12120547 0.98 RAD52 (0.46) RAD52KCNH2LMNASMN1; SMN2DPP4
Bromide SCHEMBL1307130 0.90 RAD52 (0.56) RAD52KCNH2LMNASMN1; SMN2DPP4
SCHEMBL12120528 0.88 RAD52 (0.57) RAD52KCNH2LMNASMN1; SMN2DPP4
SCHEMBL17484488 0.87 RAD52 (0.60) RAD52LMNASMN1; SMN2GNAI3GNAO1
SCHEMBL6973435 0.77 RAD52 (0.55) RAD52KCNH2LMNASMN1; SMN2CXCR4
SCHEMBL7947655 0.75 RAD52 (0.58) RAD52KCNH2LMNASMN1; SMN2CXCR4
SCHEMBL20614282 0.75 RAD52 (0.58) RAD52KCNH2LMNASMN1; SMN2CXCR4
SCHEMBL17484491 0.74 RAD52 (0.49) RAD52LMNASMN1; SMN2GNAI3GNAO1
SCHEMBL20124124 0.73 RAD52 (0.81) RAD52LMNASMN1; SMN2GNAI3GNAO1
SCHEMBL17484554 0.73 RAD52 (0.44) RAD52LMNASMN1; SMN2DPP4FAP

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
US-8053457-B2 3-imidazolyl-indoles for the treatment of proliferative diseases NOVARTIS AG (CH) 2011-11-08 US disclosed
US-20100125064-A1 3-Imidazolyl-Indoles for the Treatment of Proliferative Diseases NOVARTIS AG (CH) 2010-05-20 US disclosed
EP-2142535-A2 3-IMIDAZOLYL-INDOLES FOR THE TREATMENT OF PROLIFERATIVE DISEASES Novartis Ag (CH) 2010-01-13 EP disclosed
WO-2008119741-A2 3-IMIDAZOLYL-INDOLES FOR THE TREATMENT OF PROLIFERATIVE DISEASES NOVARTIS AG (CH) 2008-10-09 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-20100125064-A1 3-Imidazolyl-Indoles for the Treatment of Proliferative Diseases MDM4, TP53, MDM2 SIGMAR1 4605/4885RAD52 582/4885KCNH2 4415/4885

“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.