SCHEMBL5389732

SCHEMBL5389732

BrCc1ccc(Br)cc1.[MgH2]

nearest known ligand 0.52

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 4/20 0.50
TRPA1 O75762 1/20 0.50
TSHR P16473 1/20 0.50
CYP2A6 P11509 1/20 0.50
TAAR1 Q96RJ0 3/20 0.48
HTR2A P28223 1/20 0.48
IDO1 P14902 3/20 0.46
GSK3B P49841 1/20 0.44
PYCR1 P32322 2/20 0.43
CES2 O00748 1/20 0.39
CES1 P23141 1/20 0.39
KDM4E B2RXH2 1/20 0.39
ALOX15 P16050 2/20 0.38
MAPK1 P28482 1/20 0.38

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
SCHEMBL7536 0.97
Fluoride SCHEMBL29026731 0.94 ALDH1A1 (0.50) ALDH1A1TRPA1TSHRCYP2A6TAAR1
SCHEMBL27518670 0.94 ALDH1A1 (0.50) ALDH1A1TRPA1TSHRCYP2A6TAAR1
Ammonia Solution, Strong SCHEMBL28228784 0.94 ALDH1A1 (0.50) ALDH1A1TRPA1TSHRCYP2A6TAAR1
Bromide SCHEMBL29227177 0.94 ALDH1A1 (0.50) ALDH1A1TRPA1TSHRCYP2A6TAAR1
Phosphine SCHEMBL27726130 0.94 ALDH1A1 (0.50) ALDH1A1TRPA1TSHRCYP2A6TAAR1
SCHEMBL3362246 0.88 ALDH1A1 (0.50) ALDH1A1TRPA1TSHRCYP2A6TAAR1
Iodomethane SCHEMBL8216911 0.88 ALDH1A1 (0.46) ALDH1A1TRPA1TSHRCYP2A6TAAR1
SCHEMBL131361 0.83 ALDH1A1 (0.67) ALDH1A1TRPA1TSHRTAAR1HTR2A
SCHEMBL6764664 0.82 ALDH1A1 (0.47) ALDH1A1TRPA1TSHRCYP2A6TAAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115160212-A Organic luminescent material and preparation method and application thereof 吉林奥来德光电材料股份有限公司 2022-10-11 CN disclosed
US-20220119382-A1 RET INHIBITORS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF SUNSHINE LAKE PHARMA CO., LTD. (CN) 2022-04-21 US disclosed
EP-3891148-A1 RET INHIBITORS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF Sunshine Lake Pharma Co., Ltd. (CN) 2021-10-13 EP disclosed
WO-2020114494-A1 RET INHIBITORS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF SUNSHINE LAKE PHARMA CO., LTD. (CN) 2020-06-11 WO disclosed
WO-2013185740-A1 A METHOD FOR THE PREPARATION OF FINGOLIMOD ZENTIVA, K.S. (CZ) 2013-12-19 WO disclosed
CN-101074242-A Cells accumulation for sphosphonate analogs of HIV protease inhibitor compound and the same compound GILEAD SCIENCES INC (US) 2007-11-21 CN disclosed
CN-1313472-C Cellular Accumulation of Phosphonate Analogs of HIV Protease Inhibitor Compounds and Such Compounds GILEAD SCIENCES INC (US) 2007-05-02 CN disclosed
US-7186830-B2 Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2007-03-06 US disclosed
EP-1474424-A4 TRICYCLIC 2-PYRIMIDONE COMPOUNDS USEFUL AS HIV REVERSE TRANSCRIPTASE INHIBITORS BRISTOL MYERS SQUIBB CO (US) 2005-12-28 EP disclosed
CN-1649885-A Cellular Accumulation of Phosphonate Analogs of HIV Protease Inhibitor Compounds and Such Compounds GILEAD SCIENCES INC (US) 2005-08-03 CN disclosed
US-6844340-B2 Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors BRISTOL-MYERS SQUIBB COMPANY (US) 2005-01-18 US disclosed
US-20040266778-A1 Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors TARBY CHRISTINE M 2004-12-30 US disclosed
EP-1474424-A1 TRICYCLIC 2-PYRIMIDONE COMPOUNDS USEFUL AS HIV REVERSE TRANSCRIPTASE INHIBITORS Bristol-Myers Squibb Company (US) 2004-11-10 EP disclosed
US-20030162800-A1 Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors BRISTOL-MYERS SQUIBB COMPANY 2003-08-28 US disclosed
WO-2003062238-A1 TRICYCLIC 2-PYRIMIDONE COMPOUNDS USEFUL AS HIV REVERSE TRANSCRIPTASE INHIBITORS BRISTOL-MYERS SQUIBB COMPANY (US) 2003-07-31 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 (3 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-20030162800-A1 Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors TYMP, TYMS, DPYD ALDH1A1 413/4885TRPA1 4758/4885TSHR 3653/4885
US-20220119382-A1 RET INHIBITORS, PHARMACEUTICAL COMPOSITIONS AND USES THEREOF RET, SLC10A2, REL ALDH1A1 2416/4885TRPA1 496/4885TSHR 2826/4885
US-20040266778-A1 Tricyclic 2-pyrimidone compounds useful as HIV reverse transcriptase inhibitors TYMP, TYMS, DPYD ALDH1A1 413/4885TRPA1 4758/4885TSHR 3653/4885

“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.