SCHEMBL19206663

SCHEMBL19206663

CN(C)Cc1cccc(Cc2nc3c(Cc4ccccc4)[nH]c(-c4ccccc4)cn-3c2=O)c1

nearest known ligand 0.38

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ NMT1 P30419 1/20 0.38
▸ TNKS O95271 4/20 0.36
▸ AURKA O14965 2/20 0.35
▸ AURKB Q96GD4 2/20 0.35
▸ INCENP Q9NQS7 2/20 0.35
▸ TPX2 Q9ULW0 2/20 0.35
▸ PARP1 P09874 5/20 0.34
▸ SLC2A1 P11166 1/20 0.34
▸ CDC7 O00311 1/20 0.34
▸ LTB4R Q15722 1/20 0.33
▸ TSHR P16473 1/20 0.33
▸ NR4A2 P43354 1/20 0.33
▸ DCTPP1 Q9H773 1/20 0.33
▸ AVPR1B P47901 1/20 0.33
▸ ALKBH3 Q96Q83 1/20 0.33
▸ PSD A5PKW4 1/20 0.33
▸ PDE6D O43924 1/20 0.33
▸ PDE5A O76074 1/20 0.33
▸ PDE6A P16499 1/20 0.33
▸ PDE6G P18545 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
SCHEMBL19206711 0.89 HDAC1 (0.34) CDC7LTB4RALKBH3PSD
SCHEMBL492636 0.88 LTB4R (0.41) PARP1CDC7LTB4RALKBH3PSD
SCHEMBL20543611 0.88 THRB (0.42) CDC7ALKBH3
SCHEMBL19206676 0.87 LTB4R (0.38) CDC7LTB4RALKBH3PSD
SCHEMBL19206672 0.87 CDC7 (0.38) CDC7LTB4RALKBH3PSD
SCHEMBL24027765 0.86 MAPT (0.37) PARP1CDC7LTB4RALKBH3PSD
SCHEMBL19206693 0.86 POLB (0.38) CDC7LTB4RALKBH3PSD
SCHEMBL20543595 0.86 PDE3B (0.38) CDC7LTB4R
SCHEMBL20543423 0.86 PDE3B (0.38) CDC7LTB4R
SCHEMBL19206714 0.86 ALDH1A1 (0.38) PARP1CDC7LTB4RTSHRPSD

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250340923-A1 SUBSTITUTED IMIDAZO[1,2-a]PYRAZINES AS LUCIFERASE SUBSTRATES PROMEGA CORP (US) 2025-11-06 — — US claimed
US-20210254128-A1 COELENTERAZINE ANALOGUES PROMEGA CORPORATION 2021-08-19 — — US claimed
US-11015216-B2 Substituted imidazo[1,2-a]pyrazines as luciferase substrates PROMEGA CORPORATION (US) 2021-05-25 — — US claimed
US-20200263229-A1 COELENTERAZINE ANALOGUES PROMEGA CORPORATION 2020-08-20 — — US claimed
US-10308975-B2 Substituted imidazo[1,2-a]pyrazines as luciferase substrates PROMEGA CORPORATION (US) 2019-06-04 — — US claimed
EP-3416968-A1 COELENTERAZINE ANALOGUES Promega Corporation (US) 2018-12-26 — — EP claimed
US-20180223330-A1 COELENTERAZINE ANALOGUES JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT 2018-08-09 — — US claimed
WO-2017142852-A1 COELENTERAZINE ANALOGUES PROMEGA CORPORATION (US) 2017-08-24 — — WO claimed
US-20170233789-A1 COELENTERAZINE ANALOGUES JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT 2017-08-17 — — US claimed
US-20250340923-A1 SUBSTITUTED IMIDAZO[1,2-a]PYRAZINES AS LUCIFERASE SUBSTRATES PROMEGA CORP (US) 2025-11-06 — — US disclosed
US-12391973-B2 Substituted imidazo[1,2-α]pyrazines as luciferase substrates PROMEGA CORPORATION (US) 2025-08-19 — — US disclosed
US-20240068009-A1 SUBSTITUTED IMIDAZO[1,2-a]PYRAZINES AS LUCIFERASE SUBSTRATES PROMEGA CORPORATION 2024-02-29 — — US disclosed
US-11781168-B2 Process for preparing substituted imidazo[1,2-α]pyrazines PROMEGA CORPORATION (US) 2023-10-10 — — US disclosed
US-20210254128-A1 COELENTERAZINE ANALOGUES PROMEGA CORPORATION 2021-08-19 — — US disclosed
US-10308975-B2 Substituted imidazo[1,2-a]pyrazines as luciferase substrates PROMEGA CORPORATION (US) 2019-06-04 — — US disclosed
EP-3416968-A1 COELENTERAZINE ANALOGUES Promega Corporation (US) 2018-12-26 — — EP disclosed
US-20180223330-A1 COELENTERAZINE ANALOGUES JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT 2018-08-09 — — US disclosed
US-9924073-B2 Substituted imidazo[1,2-a]pyrazines as luciferase substrates and preparation method thereof PROMEGA CORPORATION (US) 2018-03-20 — — US disclosed
WO-2017142852-A1 COELENTERAZINE ANALOGUES PROMEGA CORPORATION (US) 2017-08-24 — — WO disclosed
US-20170233789-A1 COELENTERAZINE ANALOGUES JPMORGAN CHASE BANK, N.A., AS COLLATERAL AGENT 2017-08-17 — — 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-11781168-B2 Process for preparing substituted imidazo[1,2-α]pyrazines CYP4Z1, CYP2E1, CYP2F1 NMT1 4002/4885TNKS 1028/4885AURKA 187/4885
US-20210254128-A1 COELENTERAZINE ANALOGUES AADAC, GLB1, PGLS NMT1 1410/4885TNKS 3007/4885AURKA 671/4885
US-20250340923-A1 SUBSTITUTED IMIDAZO[1,2-a]PYRAZINES AS LUCIFERASE SUBSTRATES PGLS, AADAC, GLB1 NMT1 2018/4885TNKS 2799/4885AURKA 847/4885
US-11015216-B2 Substituted imidazo[1,2-a]pyrazines as luciferase substrates GLB1, PGLS, AADAC NMT1 2015/4885TNKS 3033/4885AURKA 832/4885
US-20180223330-A1 COELENTERAZINE ANALOGUES GLB1, SI, TCF7L2 NMT1 749/4885TNKS 3323/4885AURKA 4296/4885
US-20170233789-A1 COELENTERAZINE ANALOGUES GLB1, SI, TCF7L2 NMT1 749/4885TNKS 3323/4885AURKA 4296/4885
US-20200263229-A1 COELENTERAZINE ANALOGUES AADAC, GLB1, PGLS NMT1 1410/4885TNKS 3007/4885AURKA 671/4885
US-10308975-B2 Substituted imidazo[1,2-a]pyrazines as luciferase substrates AADAC, PGLS, GLB1 NMT1 1993/4885TNKS 2668/4885AURKA 851/4885
US-20240068009-A1 SUBSTITUTED IMIDAZO[1,2-a]PYRAZINES AS LUCIFERASE SUBSTRATES PGLS, AADAC, GLB1 NMT1 2018/4885TNKS 2799/4885AURKA 847/4885
US-12391973-B2 Substituted imidazo[1,2-α]pyrazines as luciferase substrates PGLS, GLB1, AADAC NMT1 2072/4885TNKS 2358/4885AURKA 844/4885

“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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