SCHEMBL376065

SCHEMBL376065

CC1(COc2ccc(N)c([N+](=O)[O-])c2)COC1

nearest known ligand 0.53

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MAPT P10636 7/20 0.48
ALDH1A1 P00352 4/20 0.48
LMNA P02545 3/20 0.48
TSHR P16473 1/20 0.44
TDP1 Q9NUW8 4/20 0.43
POLB P06746 3/20 0.43
MEN1 O00255 2/20 0.43
KMT2A Q03164 2/20 0.43
CYP3A4 P08684 1/20 0.43
ALOX15 P16050 1/20 0.43
CYP1A2 P05177 1/20 0.40
CYP2C9 P11712 1/20 0.40
CYP2C19 P33261 1/20 0.40
SMN1; SMN2 Q16637 3/20 0.40
GAA P10253 1/20 0.40
HPGD P15428 1/20 0.40
HTT P42858 1/20 0.40
NPC1 O15118 3/20 0.40
RAB9A P51151 3/20 0.40
MAPK1 P28482 2/20 0.39

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
SCHEMBL29450847 1.00 MAPT (0.48) MAPTALDH1A1LMNATSHRTDP1
SCHEMBL16634785 0.86 MAPT (0.38) MAPTALDH1A1LMNATDP1POLB
SCHEMBL14525204 0.85 MAPT (0.49) MAPTALDH1A1LMNATSHRTDP1
SCHEMBL22114715 0.80 MAPT (0.48) MAPTALDH1A1LMNATSHRTDP1
SCHEMBL1277890 0.77 MAPT (0.77) MAPTALDH1A1LMNATSHRTDP1
SCHEMBL11209297 0.77 MAPT (0.57) MAPTALDH1A1LMNATSHRTDP1
SCHEMBL11420051 0.77 MAPT (0.62) MAPTALDH1A1LMNATSHRTDP1
SCHEMBL11548169 0.75 MAPT (0.60) MAPTALDH1A1LMNATSHRTDP1
SCHEMBL11545117 0.75 MAPT (0.60) MAPTALDH1A1LMNATSHRTDP1
SCHEMBL11628266 0.75 MAPT (0.55) MAPTALDH1A1LMNATSHRTDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12600719-B2 Salt inducible kinase inhibitors THE GENERAL HOSPITAL CORPORATION (US) 2026-04-14 US disclosed
EP-4660192-A1 SALT INDUCIBLE KINASE INHIBITORS The General Hospital Corporation (US) 2025-12-10 EP disclosed
US-20240025892-A1 SALT INDUCIBLE KINASE INHIBITORS THE GENERAL HOSPITAL CORPORATION 2024-01-25 US disclosed
US-20240025892-A1 SALT INDUCIBLE KINASE INHIBITORS THE GENERAL HOSPITAL CORPORATION 2024-01-25 US disclosed
EP-4192459-A1 SALT INDUCIBLE KINASE INHIBITORS The General Hospital Corporation (US) 2023-06-14 EP disclosed
WO-2022031928-A1 SALT INDUCIBLE KINASE INHIBITORS THE GENERAL HOSPITAL CORPORATION (US) 2022-02-10 WO disclosed
CN-107382983-B Synthesis method of medicine for treating leukemia 扬州市三药制药有限公司 2020-08-07 CN disclosed
US-8518952-B2 6 substituted 2-heterocyclylamino pyrazine compounds as CHK-1 inhibitors PFIZER INC. (US) 2013-08-27 US disclosed
EP-2328890-B1 6 SUBSTITUTED 2-HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER (US) 2012-01-25 EP disclosed
EP-2328890-B1 6 SUBSTITUTED 2-HETEROCYCLYLAMINO PYRAZINE COMPOUNDS AS CHK-1 INHIBITORS PFIZER (US) 2012-01-25 EP disclosed
EP-1641780-B1 PROCESSES FOR THE PREPARATION OF 1- [(BENZOIMIDAZOLE-1YL) QUINOLIN-8-YL] PIPERIDIN-4-YLAMINE DERIVATIVES PFIZER PROD INC (US) 2008-11-12 EP disclosed
US-20070088032-A1 Processes for the Preparation of Benzoimidazole Derivatives TOM NORMA J 2007-04-19 US disclosed
US-20070088032-A1 Processes for the Preparation of Benzoimidazole Derivatives TOM NORMA J 2007-04-19 US disclosed
US-20070088032-A1 Processes for the Preparation of Benzoimidazole Derivatives TOM NORMA J 2007-04-19 US disclosed
US-7183414-B2 Processes for the preparation of benzoimidazole derivatives PFIZER INC (US) 2007-02-27 US disclosed
US-7183414-B2 Processes for the preparation of benzoimidazole derivatives PFIZER INC (US) 2007-02-27 US disclosed
US-7183414-B2 Processes for the preparation of benzoimidazole derivatives PFIZER INC (US) 2007-02-27 US disclosed
EP-1641780-A1 PROCESSES FOR THE PREPARATION OF 1- [(BENZOIMIDAZOLE-1YL) QUINOLIN-8-YL] PIPERIDIN-4-YLAMINE DERIVATIVES Pfizer Products Incorporated (US) 2006-04-05 EP disclosed
US-20050020625-A1 Processes for the preparation of benzoimidazole derivatives PFIZER INC 2005-01-27 US disclosed
WO-2004113322-A1 PROCESSES FOR THE PREPARATION OF 1-[(BENZOIMIDAZOLE-1YL) QUINOLIN-8-YL] PIPERIDIN-4-YLAMINE DERIVATIVES PFIZER PRODUCTS INC. (US) 2004-12-29 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 (4 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-12600719-B2 Salt inducible kinase inhibitors GRK6, SGK1, CSNK1A1 MAPT 4456/4885ALDH1A1 3553/4885LMNA 2900/4885
US-20070088032-A1 Processes for the Preparation of Benzoimidazole Derivatives CCNI, CCNT1, CCNE1 MAPT 4057/4885ALDH1A1 292/4885LMNA 2111/4885
US-20240025892-A1 SALT INDUCIBLE KINASE INHIBITORS SGK1, SGK2, SIK1 MAPT 1834/4885ALDH1A1 4420/4885LMNA 3886/4885
US-20050020625-A1 Processes for the preparation of benzoimidazole derivatives CCNI, CCNT1, CCNE1 MAPT 4068/4885ALDH1A1 334/4885LMNA 2144/4885

“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.