SCHEMBL5560844

SCHEMBL5560844

O=c1c(Cc2ccco2)nc2c(Cc3ccccc3)[nH]c(-c3ccc(O)cc3)cn1-2

nearest known ligand 0.37

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ ALDH1A1 P00352 6/20 0.37
▸ ADORA2B P29275 7/20 0.36
▸ ADORA2A P29274 6/20 0.36
▸ ABCB1 P08183 1/20 0.35
▸ TSHR P16473 2/20 0.34
▸ LMNA P02545 2/20 0.33
▸ ALOX15 P16050 1/20 0.33
▸ HSD17B10 Q99714 1/20 0.33
▸ NPSR1 Q6W5P4 1/20 0.33
▸ KDM4E B2RXH2 1/20 0.33
▸ GAA P10253 1/20 0.33
▸ HPGD P15428 1/20 0.33
▸ CASP3 P42574 1/20 0.33
▸ RAB9A P51151 1/20 0.33
▸ SENP8 Q96LD8 1/20 0.33
▸ SENP7 Q9BQF6 1/20 0.33
▸ SENP6 Q9GZR1 1/20 0.33
▸ RCE1 Q9Y256 1/20 0.33
▸ ADORA3 P0DMS8 1/20 0.33
▸ ADORA1 P30542 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
SCHEMBL19810310 0.93 ADORA2B (0.38) ALDH1A1ADORA2BADORA2ATSHRLMNA
SCHEMBL2670126 0.93 ALDH1A1 (0.39) ALDH1A1ADORA2BADORA2ATSHRLMNA
SCHEMBL28394541 0.92 ADORA2B (0.35) ALDH1A1ADORA2BADORA2ATSHRLMNA
SCHEMBL954434 0.91 ABCB1 (0.41) ALDH1A1ADORA2AABCB1HSD17B10KDM4E
SCHEMBL20211769 0.91 TSHR (0.36) ALDH1A1ADORA2BADORA2ATSHRLMNA
SCHEMBL28888591 0.91 PSD (0.38) ALDH1A1ADORA2BADORA2ATSHRLMNA
SCHEMBL28391210 0.91 PRNP (0.36) ALDH1A1ADORA2BADORA2ATSHRLMNA
SCHEMBL19810320 0.91 LTB4R (0.36) ALDH1A1ADORA2BADORA2ATSHRLMNA
SCHEMBL19810212 0.91 ALDH1A1 (0.38) ALDH1A1ADORA2BADORA2ATSHRLMNA
SCHEMBL64690 0.90 ABCB1 (0.42) ALDH1A1ADORA2AABCB1HSD17B10KDM4E

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 68 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-10669280-B2 Coelenterazine analogues PROMEGA CORPORATION (US) 2020-06-02 — — US claimed
US-10428075-B2 Coelenterazine analogues PROMEGA CORPORATION (US) 2019-10-01 — — US claimed
EP-3490991-A1 COELENTERAZINE ANALOGUES Promega Corporation (US) 2019-06-05 — — EP claimed
US-20180334463-A1 COELENTERAZINE ANALOGUES JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT 2018-11-22 — — US claimed
US-10000500-B2 Coelenterazine analogues PROMEGA CORPORATION (US) 2018-06-19 — — US claimed
WO-2018022865-A1 COELENTERAZINE ANALOGUES PROMEGA CORPORATION (US) 2018-02-01 — — WO claimed
US-20180030059-A1 COELENTERAZINE ANALOGUES JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT 2018-02-01 — — US claimed
US-12612411-B1 Imidazopyrazine derivatives, process for preparation thereof, and their uses as luciferins INSTITUT PASTEUR (FR) 2026-04-28 — — US disclosed
US-12576164-B2 Imidazopyrazine derivatives, process for preparation thereof, and their uses as luciferins INSTITUT PASTEUR (FR) 2026-03-17 — — US disclosed
US-12570654-B2 Nanoluc suicide substrates PROMEGA CORPORATION (US) 2026-03-10 — — US disclosed
EP-4608852-A1 NOVEL FLUORESCENT AND BIOLUMINESCENT PROTEINS AND REPORTER SYSTEMS FOR RATIOMETRIC MEASUREMENT OF LUMINESCENCE Urban, Jörg (DE) 2025-09-03 — — EP disclosed
EP-3964501-B1 IMIDAZOPYRAZINE DERIVATIVES, PROCESS FOR PREPARATION THEREOF, AND THEIR USES AS LUCIFERINS PASTEUR INSTITUT (FR) 2024-09-04 — — EP disclosed
US-20240197923-A1 IMIDAZOPYRAZINE DERIVATIVES, PROCESS FOR PREPARATION THEREOF, AND THEIR USES AS LUCIFERINS INSTITUT PASTEUR (FR) 2024-06-20 — — US disclosed
US-8669103-B2 Oplophorus-derived luciferases, novel coelenterazine substrates, and methods of use PROMEGA CORPORATION (US) 2014-03-11 — — US disclosed
US-8669103-B2 Oplophorus-derived luciferases, novel coelenterazine substrates, and methods of use PROMEGA CORPORATION (US) 2014-03-11 — — US disclosed
US-20120174242-A1 OPLOPHORUS-DERIVED LUCIFERASES, NOVEL COELENTERAZINE SUBSTRATES, AND METHODS OF USE JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT 2012-07-05 — — US disclosed
US-20120174242-A1 OPLOPHORUS-DERIVED LUCIFERASES, NOVEL COELENTERAZINE SUBSTRATES, AND METHODS OF USE JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT 2012-07-05 — — US disclosed
WO-2012061529-A1 NOVEL COELENTERAZINE SUBSTRATES AND METHODS OF USE PROMEGA CORPORATION (US) 2012-05-10 — — WO disclosed
US-20120117667-A1 NOVEL COELENTERAZINE SUBSTRATES AND METHODS OF USE JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT 2012-05-10 — — US disclosed
US-20120117667-A1 NOVEL COELENTERAZINE SUBSTRATES AND METHODS OF USE JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT 2012-05-10 — — 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 (10 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-10000500-B2 Coelenterazine analogues GLB1, TCF7L2, SI ALDH1A1 3416/4885ADORA2B 3223/4885ADORA2A 2012/4885
US-12576164-B2 Imidazopyrazine derivatives, process for preparation thereof, and their uses as luciferins LUC7L2, HLCS, LANCL1 ALDH1A1 659/4885ADORA2B 1588/4885ADORA2A 1256/4885
US-20120117667-A1 NOVEL COELENTERAZINE SUBSTRATES AND METHODS OF USE RNGTT, UPF1, NSUN2 ALDH1A1 4348/4885ADORA2B 4368/4885ADORA2A 3255/4885
US-10669280-B2 Coelenterazine analogues GLB1, SI, TCF7L2 ALDH1A1 3541/4885ADORA2B 3105/4885ADORA2A 1970/4885
US-10428075-B2 Coelenterazine analogues GLB1, SI, TCF7L2 ALDH1A1 3541/4885ADORA2B 3105/4885ADORA2A 1970/4885
US-12612411-B1 Imidazopyrazine derivatives, process for preparation thereof, and their uses as luciferins LUC7L2, MRPL21, CRY1 ALDH1A1 1484/4885ADORA2B 2182/4885ADORA2A 1556/4885
US-20180030059-A1 COELENTERAZINE ANALOGUES GLB1, SI, TCF7L2 ALDH1A1 3541/4885ADORA2B 3105/4885ADORA2A 1970/4885
US-12570654-B2 Nanoluc suicide substrates NR3C1, LUC7L2, L3MBTL1 ALDH1A1 1718/4885ADORA2B 3101/4885ADORA2A 2271/4885
US-20240197923-A1 IMIDAZOPYRAZINE DERIVATIVES, PROCESS FOR PREPARATION THEREOF, AND THEIR USES AS LUCIFERINS NISCH, HLCS, CYP3A5 ALDH1A1 972/4885ADORA2B 2895/4885ADORA2A 1755/4885
US-20180334463-A1 COELENTERAZINE ANALOGUES GLB1, SI, TCF7L2 ALDH1A1 3541/4885ADORA2B 3105/4885ADORA2A 1970/4885

“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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