SCHEMBL398803

SCHEMBL398803

Cc1cc([N+](=O)[O-])ccc1N1CCN(C)CC1

nearest known ligand 0.61

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 8/20 0.61
SIRT6 Q8N6T7 1/20 0.59
LMNA P02545 4/20 0.59
GAA P10253 2/20 0.59
WDR5 P61964 7/20 0.57
KMT2A Q03164 3/20 0.56
MEN1 O00255 2/20 0.56
HTT P42858 2/20 0.56
CYP1A2 P05177 2/20 0.56
CYP3A4 P08684 2/20 0.56
CYP2C19 P33261 2/20 0.56
CYP2D6 P10635 1/20 0.56
CYP2C9 P11712 1/20 0.56
SMN1; SMN2 Q16637 1/20 0.55
POLB P06746 1/20 0.55
KDM4E B2RXH2 1/20 0.54

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
SCHEMBL30410222 1.00 ALDH1A1 (0.61) ALDH1A1SIRT6LMNAGAAWDR5
SCHEMBL21590163 0.94 LMNA (0.63) ALDH1A1SIRT6LMNAGAAWDR5
SCHEMBL7049102 0.89 GAA (0.60) ALDH1A1LMNAGAAKMT2AMEN1
SCHEMBL427403 0.88 SIRT6 (0.59) ALDH1A1SIRT6LMNAGAAWDR5
SCHEMBL10036126 0.87 ALDH1A1 (0.52) ALDH1A1SIRT6LMNAGAAWDR5
SCHEMBL328462 0.87 WDR5 (0.49) ALDH1A1SIRT6LMNAGAAWDR5
SCHEMBL30464731 0.87 WDR5 (0.49) ALDH1A1SIRT6LMNAGAAWDR5
SCHEMBL10036447 0.87 KMT2A (0.50) ALDH1A1SIRT6LMNAGAAWDR5
Hydrochloric Acid SCHEMBL5827767 0.86 SIRT6 (0.58) ALDH1A1SIRT6LMNAGAAWDR5
SCHEMBL242441 0.86 GAA (0.69) ALDH1A1LMNAGAAKMT2AMEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4619406-A1 TRICYCLIC COMPOUNDS Schrödinger, Inc. (US) 2025-09-24 EP disclosed
WO-2025042408-A1 METHODS OF TREATING CANCER SCHRÖDINGER, INC. (US) 2025-02-27 WO disclosed
WO-2024107393-A1 TRICYCLIC COMPOUNDS SCHRÖDINGER, INC. (US) 2024-05-23 WO disclosed
EP-3543242-B1 8,9-DIHYDROIMIDAZOLE[1,2-A]PYRIMIDO[5,4-E]PYRIMIDINE-5(6H)-KETONE COMPOUND IMPACT THERAPEUTICS SHANGHAI INC (CN) 2024-01-03 EP disclosed
WO-2023217201-A2 NOVEL PYRIMIDO-HETEROCYCLIC NOVEL COMPOUND SERVING AS WEE1 INHIBITOR AND APPLICATION THEREOF 杭州德睿智药科技有限公司 2023-11-16 WO disclosed
CN-116143773-B 2-amino-4-thiazolylpyrimidine compound and preparation method and application thereof 中国药科大学 2023-07-21 CN disclosed
CN-113614087-B WEE1 inhibitor and preparation and application thereof 首药控股(北京)股份有限公司 2023-06-02 CN disclosed
CN-116143773-A 2-amino-4-thiazolylpyrimidine compound and preparation method and application thereof 中国药科大学 2023-05-23 CN disclosed
US-11643396-B2 BRD4-kinase inhibitors as cancer therapeutics H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. (US) 2023-05-09 US disclosed
US-11643396-B2 BRD4-kinase inhibitors as cancer therapeutics H. LEE MOFFITT CANCER CENTER AND RESEARCH INSTITUTE, INC. (US) 2023-05-09 US disclosed
EP-1694652-A1 STEREOISOMERS AND STEREOISOMERIC MIXTURES OF 1-(2,4-PYRIMIDINEDIAMINO)-2-CYCLOPENTANECARBOXAMIDE SYNTHETIC INTERMEDIATES Rigel Pharmaceuticals, Inc. (US) 2006-08-30 EP disclosed
US-20060167249-A1 Stereoisomerically enriched 3-aminocarbonyl bicycloheptene pyrimidinediamine compounds and their uses RIGEL PHARMACEUTICALS, INC. (US) 2006-07-27 US disclosed
WO-2006055561-A2 STEREOISOMERICALLY ENRICHED 3-AMINOCARBONYL BICYCLOHEPTENE PYRIMIDINEDIAMINE COMPOUNDS AND THEIR USES RIGEL PHARMACEUTICALS, INC. (US) 2006-05-26 WO disclosed
US-20060035891-A1 Cycloalkyl substituted pyrimidinediamine compounds and their uses MIDCAP FINANCIAL TRUST 2006-02-16 US disclosed
US-20050288515-A1 Chemical compounds SMITHLINE BEECHAM CORPORATION 2005-12-29 US disclosed
WO-2005118544-A2 CYCLOALKYL SUBSTITUTED PYRIMIDINEDIAMINE COMPOUNDS AND THEIR USES RIGEL PHARMACEUTICALS, INC. (US) 2005-12-15 WO disclosed
US-20050192301-A1 Stereoisomers and stereoisomeric mixtures of 1-(2,4-pyrimidinediamino)-2-cyclopentanecarboxamide synthetic intermediates MIDCAP FINANCIAL TRUST 2005-09-01 US disclosed
WO-2005063722-A1 STEREOISOMERS AND STEREOISOMERIC MIXTURES OF 1-(2,4-PYRIMIDINEDIAMINO)-2-CYCLOPENTANECARBOXAMIDE SYNTHETIC INTERMEDIATES RIGEL PHARMACEUTICALS, INC. (US) 2005-07-14 WO disclosed
EP-1551813-A2 CHEMICAL COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2005-07-13 EP disclosed
WO-2004032882-A2 CHEMICAL COMPOUNDS SMITHKLINE BEECHAM CORPORATION (US) 2004-04-22 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 (5 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-20050192301-A1 Stereoisomers and stereoisomeric mixtures of 1-(2,4-pyrimidinediamino)-2-cyclopentanecarboxamide synthetic intermediates PCNA, PAICS, DPYD ALDH1A1 1230/4885SIRT6 2193/4885LMNA 1781/4885
US-20060035891-A1 Cycloalkyl substituted pyrimidinediamine compounds and their uses MKI67, PCNA, TK1 ALDH1A1 1807/4885SIRT6 1987/4885LMNA 2917/4885
US-11643396-B2 BRD4-kinase inhibitors as cancer therapeutics BRD4, BICRA, BRDT ALDH1A1 3541/4885SIRT6 340/4885LMNA 3929/4885
US-20060167249-A1 Stereoisomerically enriched 3-aminocarbonyl bicycloheptene pyrimidinediamine compounds and their uses MKI67, PCNA, CCNI ALDH1A1 705/4885SIRT6 2608/4885LMNA 3220/4885
US-20050288515-A1 Chemical compounds CDK4, CDK2, CDK3 ALDH1A1 1300/4885SIRT6 1630/4885LMNA 3033/4885

“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.