Bromide

Bromide

SCHEMBL15901561

Cc1cc2nc3c(=O)n(CCNC(=O)OC(C)(C)C)c(=O)nc-3n(CC[N+](C)(C)CCNC(=O)OC(C)(C)C)c2cc1C.[Br-]

nearest known ligand 0.42

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 17)

geneUniProtsupporting neighboursconfidence
▸ BRD4 O60885 11/20 0.42
▸ KDM4E B2RXH2 1/20 0.38
▸ MEN1 O00255 1/20 0.38
▸ USP2 O75604 1/20 0.38
▸ MAPT P10636 1/20 0.38
▸ IDO1 P14902 1/20 0.38
▸ HTT P42858 1/20 0.38
▸ KMT2A Q03164 1/20 0.38
▸ RXFP1 Q9HBX9 1/20 0.38
▸ TDP1 Q9NUW8 1/20 0.38
▸ SCD O00767 1/20 0.36
▸ DYRK1A Q13627 1/20 0.33
▸ STING1 Q86WV6 2/20 0.32
▸ CYP3A4 P08684 1/20 0.32
▸ CYP2D6 P10635 1/20 0.32
▸ CYP2C9 P11712 1/20 0.32
▸ CYP2C19 P33261 1/20 0.32

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
SCHEMBL22653180 0.99 BRD4 (0.42) BRD4KDM4EMEN1USP2MAPT
SCHEMBL15901081 0.91 BRD4 (0.48) BRD4KDM4EMEN1USP2MAPT
SCHEMBL15908088 0.81 KDM4E (0.37) KDM4EMEN1USP2MAPTIDO1
Bromide SCHEMBL17254518 0.81 KDM4E (0.42) KDM4EMEN1USP2MAPTIDO1
SCHEMBL16476439 0.80 KDM4E (0.42) KDM4EMEN1USP2MAPTIDO1
SCHEMBL15908087 0.77 KDM4E (0.40) KDM4EMEN1USP2MAPTIDO1
SCHEMBL15908095 0.76 KDM4E (0.43) KDM4EMEN1USP2MAPTIDO1
SCHEMBL19405681 0.76 MEN1 (0.65) BRD4KDM4EMEN1USP2MAPT
SCHEMBL15908041 0.76 MEN1 (0.43) KDM4EMEN1USP2MAPTIDO1
SCHEMBL15908133 0.76 CYP1A2 (0.40) KDM4EMEN1USP2MAPTIDO1

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-9745302-B2 10H-benzo[g]pteridine-2,4-dione derivatives, method for the production thereof, and use thereof TRIOPTOTEC GMBH (DE) 2017-08-29 — — US disclosed
US-20160176877-A1 10H-BENZO[G]PTERIDINE-2,4-DIONE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, AND USE THEREOF TRIOPTOTEC GMBH 2016-06-23 — — US disclosed
US-9241995-B2 10H-benzo[G]pteridine-2,4-dione derivatives, method for the production thereof, and use thereof TRIOPTOTEC GMBH (DE) 2016-01-26 — — US disclosed
US-20140212459-A1 10H-BENZO[G]PTERIDINE-2,4-DIONE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, AND USE THEREOF TRIOPTOTEC GMBH (DE) 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 (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-20160176877-A1 10H-BENZO[G]PTERIDINE-2,4-DIONE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, AND USE THEREOF DHPS, DOHH, PAH BRD4 137/4885KDM4E 376/4885MEN1 1722/4885
US-20140212459-A1 10H-BENZO[G]PTERIDINE-2,4-DIONE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF, AND USE THEREOF DHPS, DOHH, PAH BRD4 137/4885KDM4E 376/4885MEN1 1722/4885

“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.

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