SCHEMBL10196956

SCHEMBL10196956

O=c1c(Cc2ccc3ccccc3c2)nc2c(Cc3ccccc3)[nH]c(-c3ccc(O)cc3)cn1-2

nearest known ligand 0.38

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ ABCB1 P08183 1/20 0.38
▸ CDC7 O00311 2/20 0.35
▸ ALOX5 P09917 1/20 0.35
▸ CHEK2 O96017 1/20 0.35
▸ PARP1 P09874 2/20 0.34
▸ XDH P47989 1/20 0.34
▸ GABRA1 P14867 2/20 0.34
▸ GABRB2 P47870 2/20 0.34
▸ PTGDR2 Q9Y5Y4 2/20 0.34
▸ ESR1 P03372 1/20 0.34
▸ BACE1 P56817 1/20 0.33
▸ ADORA3 P0DMS8 1/20 0.33
▸ ADORA1 P30542 1/20 0.33
▸ ALDH1A1 P00352 1/20 0.33
▸ NPY5R Q15761 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
SCHEMBL19206729 0.93 BACE1 (0.36) CDC7CHEK2XDHGABRA1GABRB2
SCHEMBL12293879 0.93 ABCB1 (0.42) ABCB1CDC7PARP1XDHADORA3
SCHEMBL64690 0.93 ABCB1 (0.42) ABCB1CDC7PARP1XDHADORA3
SCHEMBL954434 0.92 ABCB1 (0.41) ABCB1CDC7PARP1XDHADORA3
SCHEMBL2680751 0.91 ABCB1 (0.40) ABCB1CDC7PARP1XDHADORA3
SCHEMBL10196910 0.90 PARP1 (0.38) ABCB1CDC7PARP1XDHADORA3
SCHEMBL17696238 0.89 PTGS2 (0.33) CDC7CHEK2XDHGABRA1GABRB2
SCHEMBL21531540 0.89 KDM4E (0.37) ABCB1ALDH1A1
SCHEMBL20841761 0.88 ABCB1 (0.39) ABCB1CDC7GABRA1GABRB2ADORA3
SCHEMBL20841749 0.88 ABCB1 (0.39) ABCB1CDC7PARP1XDHPTGDR2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240239803-A1 SYNTHESIS OF COELENTERAZINE INTERNATIONAL PAPER COMPANY 2024-07-18 — — US disclosed
US-20240239803-A1 SYNTHESIS OF COELENTERAZINE INTERNATIONAL PAPER COMPANY 2024-07-18 — — US disclosed
US-20210332044-A1 SYNTHESIS OF COELENTERAZINE SYNTHESIS INTERMEDIATE INTERNATIONAL PAPER COMPANY (US) 2021-10-28 — — US disclosed
US-11078200-B2 Synthesis of coelenterazine INTERNATIONAL PAPER COMPANY (US) 2021-08-03 — — US disclosed
US-11008326-B2 Synthesis of coelenterazine INTERNATIONAL PAPER COMPANY (US) 2021-05-18 — — US disclosed
US-20210070762-A1 SYNTHESIS OF COELENTERAZINE INTERNATIONAL PAPER COMPANY (US) 2021-03-11 — — US disclosed
US-10906911-B2 — — 2021-02-02 — — US disclosed
US-20200239471-A1 SYNTHESIS OF COELENTERAZINE ALLY BANK, AS COLLATERAL AGENT 2020-07-30 — — US disclosed
US-9645128-B2 Substituted imidazo[1,2-A]pyrazines for measuring a transcription activity JNC CORPORATION (JP) 2017-05-09 — — US disclosed
US-9645128-B2 Substituted imidazo[1,2-A]pyrazines for measuring a transcription activity JNC CORPORATION (JP) 2017-05-09 — — US disclosed
US-8765921-B2 Coelenterazine analogs and manufacturing method thereof JNC CORPORATION (JP) 2014-07-01 — — US disclosed
US-20140024058-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF TOKYO INSTITUTE OF TECHNOLOGY (JP) 2014-01-23 — — US disclosed
US-20140024058-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF TOKYO INSTITUTE OF TECHNOLOGY (JP) 2014-01-23 — — US disclosed
US-8546568-B2 Coelenterazine analogs and manufacturing method thereof JNC CORPORATION (JP) 2013-10-01 — — US disclosed
US-8546568-B2 Coelenterazine analogs and manufacturing method thereof JNC CORPORATION (JP) 2013-10-01 — — US disclosed
US-20120035070-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF TOKYO INSTITUTE OF TECHNOLOGY (JP) 2012-02-09 — — US disclosed
US-20120035070-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF TOKYO INSTITUTE OF TECHNOLOGY (JP) 2012-02-09 — — US disclosed
WO-2010090319-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF チッソ株式会社 (JP) 2010-08-12 — — WO disclosed
US-20100105090-A1 SECRETED LUCIFERASE MLUC7 AND USE THEREOF BAYER HEALTHCARE AG (DE) 2010-04-29 — — US disclosed
US-20100105090-A1 SECRETED LUCIFERASE MLUC7 AND USE THEREOF BAYER HEALTHCARE AG (DE) 2010-04-29 — — 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 (9 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-20100105090-A1 SECRETED LUCIFERASE MLUC7 AND USE THEREOF LUC7L2, MRPL37, TCF7 ABCB1 3223/4885CDC7 526/4885ALOX5 4534/4885
US-11008326-B2 Synthesis of coelenterazine ACHE, UROD, DDT ABCB1 1652/4885CDC7 805/4885ALOX5 804/4885
US-20240239803-A1 SYNTHESIS OF COELENTERAZINE ACHE, UROD, DDT ABCB1 1652/4885CDC7 805/4885ALOX5 804/4885
US-20210070762-A1 SYNTHESIS OF COELENTERAZINE ACHE, UROD, DDT ABCB1 1652/4885CDC7 805/4885ALOX5 804/4885
US-10906911-B2 — ACHE, UROD, SI ABCB1 1174/4885CDC7 1170/4885ALOX5 454/4885
US-20120035070-A1 COELENTERAZINE ANALOGS AND MANUFACTURING METHOD THEREOF GLB1, CEL, SI ABCB1 1068/4885CDC7 2192/4885ALOX5 1352/4885
US-11078200-B2 Synthesis of coelenterazine ACHE, UROD, DDT ABCB1 1652/4885CDC7 805/4885ALOX5 804/4885
US-20200239471-A1 SYNTHESIS OF COELENTERAZINE ACHE, UROD, DDT ABCB1 1652/4885CDC7 805/4885ALOX5 804/4885
US-20210332044-A1 SYNTHESIS OF COELENTERAZINE SYNTHESIS INTERMEDIATE DCXR, SI, UROD ABCB1 1854/4885CDC7 853/4885ALOX5 656/4885

“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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