Bromide

Bromide

SCHEMBL814176

CC(C)c1cccc(C(C)C)c1NCCCN(C)CCNc1c(C(C)C)cccc1C(C)C.[Br-].[Br-].[Co+2]

nearest known ligand 0.39

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ACHECHKACHRM1CHRM2CHRM3CHRM4CHRM5CHRNA1CHRNB1CHRNDCHRNECHRNGHRH2OPRM1

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 12)

geneUniProtsupporting neighboursconfidence
ACHE known ✓ P22303 2/20 0.37
SMN1; SMN2 Q16637 1/20 0.39
BCHE P06276 2/20 0.37
NPC1 O15118 1/20 0.36
POLB P06746 1/20 0.36
SLC2A1 P11166 1/20 0.36
APOBEC3A P31941 1/20 0.36
RAD52 P43351 1/20 0.36
RAB9A P51151 1/20 0.36
KMT2A Q03164 1/20 0.36
APOBEC3G Q9HC16 1/20 0.36
SOAT1 P35610 1/20 0.35

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
Hydrochloric Acid SCHEMBL812989 0.97 SMN1; SMN2 (0.39) SMN1; SMN2BCHEACHENPC1POLB
Bromide SCHEMBL812416 0.97 SMN1; SMN2 (0.41) SMN1; SMN2BCHEACHENPC1POLB
Hydrochloric Acid SCHEMBL814419 0.94 SMN1; SMN2 (0.41) SMN1; SMN2BCHEACHENPC1POLB
Bromide SCHEMBL813969 0.94 SMN1; SMN2 (0.42) SMN1; SMN2KMT2ASOAT1
Hydrochloric Acid SCHEMBL813185 0.91 SMN1; SMN2 (0.42) SMN1; SMN2KMT2ASOAT1
Hydrochloric Acid SCHEMBL812536 0.91 SMN1; SMN2 (0.42) SMN1; SMN2KMT2ASOAT1
SCHEMBL813988 0.89 SMN1; SMN2 (0.44) SMN1; SMN2KMT2ASOAT1
SCHEMBL814399 0.89 SMN1; SMN2 (0.44) SMN1; SMN2KMT2ASOAT1
SCHEMBL813193 0.89 SMN1; SMN2 (0.44) SMN1; SMN2KMT2ASOAT1
SCHEMBL812879 0.89 SMN1; SMN2 (0.44) SMN1; SMN2KMT2ASOAT1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8058372-B2 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. (US) 2011-11-15 US disclosed
US-20080319147-A1 Catalyst Composition II EXXONMOBIL CHEMICAL PATENTS INC. 2008-12-25 US disclosed
US-7371803-B2 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. (US) 2008-05-13 US disclosed
US-20070066776-A1 Catalyst composition II SOLAN GREGORY A 2007-03-22 US disclosed
US-7189791-B2 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. (US) 2007-03-13 US disclosed
EP-1641842-A2 POLYMERIZATION AND OLIGOMERIZATION CATALYST WITH TRIDENTATE OR TETRADENTATE LIGAND Exxonmobil Chemical Patents Inc. (US) 2006-04-05 EP disclosed
US-20040266961-A1 Catalyst composition II EXXONMOBIL CHEMICAL PATENTS INC. 2004-12-30 US disclosed
WO-2004106390-A2 POLYMERIZATION AND OLIGOMERIZATION CATALYST WITH TRIDENTATE OR TETRADENTATE LIGAND EXXONMOBIL CHEMICAL PATENTS INC. (US) 2004-12-09 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-20040266961-A1 Catalyst composition II MLX, CBX2, BMX ACHE 3557/4885SMN1; SMN2 1110/4885BCHE 3414/4885

“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.