SCHEMBL374222

SCHEMBL374222

CCN1CCN(c2ccc([N+](=O)[O-])cc2)CC1

nearest known ligand 0.69

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
SIRT6 Q8N6T7 2/20 0.68
POLB P06746 3/20 0.63
MAPT P10636 4/20 0.62
ALDH1A1 P00352 4/20 0.61
LMNA P02545 2/20 0.61
SMN1; SMN2 Q16637 1/20 0.61
KMT2A Q03164 2/20 0.60
HPGD P15428 1/20 0.60
ADRB1 P08588 1/20 0.58
MEN1 O00255 1/20 0.58

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
SCHEMBL1045292 0.87 SIRT6 (0.69) SIRT6POLBMAPTALDH1A1LMNA
SCHEMBL6151230 0.86 SIRT6 (0.81) SIRT6POLBMAPTALDH1A1LMNA
SCHEMBL15271381 0.86 SIRT6 (0.81) SIRT6POLBMAPTALDH1A1LMNA
SCHEMBL6945690 0.84 SIRT6 (0.65) SIRT6POLBMAPTALDH1A1LMNA
SCHEMBL25797013 0.83 SIRT6 (0.59) SIRT6POLBMAPTALDH1A1LMNA
SCHEMBL943807 0.83 SIRT6 (0.62) SIRT6POLBMAPTALDH1A1LMNA
SCHEMBL5741339 0.83 SIRT6 (0.62) SIRT6POLBMAPTALDH1A1LMNA
SCHEMBL27580383 0.83 SIRT6 (0.62) SIRT6POLBMAPTALDH1A1LMNA
SCHEMBL2730000 0.82 KDM4E (0.63) SIRT6POLBMAPTALDH1A1LMNA
SCHEMBL10511652 0.82 LMNA (0.68) SIRT6POLBMAPTALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-1257896-C Funcitonal molecule material containing four tertiary amine branches and preparation method UNIV FUDAN (CN) 2006-05-31 CN claimed
CN-1539833-A Funcitonal molecule material containing four tertiary amine branches and preparation method 复旦大学 2004-10-27 CN claimed
EP-4676486-A1 METHODS OF TREATING SKELETAL DYSPLASIAS QED Therapeutics, Inc. (US) 2026-01-14 EP disclosed
US-12357632-B2 Methods of treating cholangiocarcinoma QED THERAPEUTICS, INC. (US) 2025-07-15 US disclosed
WO-2025090870-A1 INFIGRATINIB AND METABOLITES THEREOF FOR USE IN METHODS OF TREATING SKELETAL DISORDERS QED THERAPEUTICS, INC. (US) 2025-05-01 WO disclosed
US-20250101002-A1 DEUTERATED INFIGRATINIB COMPOUNDS Ferro Therapeutics, Inc. 2025-03-27 US disclosed
WO-2024186882-A1 METHODS OF TREATING SKELETAL DYSPLASIAS QED THERAPEUTICS, INC. (US) 2024-09-12 WO disclosed
WO-2024093681-A1 USE OF INFIGRATINIB IN TREATING GASTRIC CANCER AND ADENOCARCINOMA QED医药股份有限公司 2024-05-10 WO disclosed
CN-117982507-A Use of inflictinib in the treatment of gastric and adenocarcinoma QED医药股份有限公司 2024-05-07 CN disclosed
US-20240009193-A1 METHODS OF TREATING ACHONDROPLASIA CALCILYTIX THERAPEUTICS INC. 2024-01-11 US disclosed
EP-4262774-A1 METHODS OF TREATING ACHONDROPLASIA QED Therapeutics, Inc. (US) 2023-10-25 EP disclosed
US-7071216-B2 Substituted benz-azoles and methods of their use as inhibitors of Raf kinase CHIRON CORPORATION (US) 2006-07-04 US disclosed
CN-1257896-C Funcitonal molecule material containing four tertiary amine branches and preparation method UNIV FUDAN (CN) 2006-05-31 CN disclosed
WO-2006000420-A1 PYRIMIDINE UREA DERIVATIVES AS KINASE INHIBITORS NOVARTIS AG (CH) 2006-01-05 WO disclosed
WO-2005032548-A1 SUBSTITUTED BENZAZOLES AND USE THEREOF AS INHIBITORS OF RAF KINASE CHIRON CORPORATION (US) 2005-04-14 WO disclosed
EP-1499311-A1 SUBSTITUTED BENZAZOLES AND USE THEREOF AS RAF KINASE INHIBITORS Chiron Corporation (US) 2005-01-26 EP disclosed
CN-1539833-A Funcitonal molecule material containing four tertiary amine branches and preparation method 复旦大学 2004-10-27 CN disclosed
US-20040122237-A1 Substituted benzazoles and methods of their use as inhibitors of Raf kinase NOVARTIS AG (CH) 2004-06-24 US disclosed
US-20040087626-A1 Substituted benz-azoles and methods of their use as inhibitors of Raf kinase NOVARTIS AG (CH) 2004-05-06 US disclosed
WO-2003082272-A1 SUBSTITUTED BENZAZOLES AND USE THEREOF AS RAF KINASE INHIBITORS CHIRON CORPORATION (US) 2003-10-09 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-20240009193-A1 METHODS OF TREATING ACHONDROPLASIA FGFR3, FGF2, FGF1 SIRT6 289/4885POLB 1158/4885MAPT 3391/4885
US-20040122237-A1 Substituted benzazoles and methods of their use as inhibitors of Raf kinase BRAF, RAF1, ARAF SIRT6 3252/4885POLB 1655/4885MAPT 3948/4885
US-20040087626-A1 Substituted benz-azoles and methods of their use as inhibitors of Raf kinase BRAF, RAF1, ARAF SIRT6 3316/4885POLB 1501/4885MAPT 3981/4885
US-12357632-B2 Methods of treating cholangiocarcinoma KRAS, SLC10A2, SLC10A1 SIRT6 3001/4885POLB 1489/4885MAPT 4676/4885
US-20250101002-A1 DEUTERATED INFIGRATINIB COMPOUNDS FGFR3, FGFR1, ABL1 SIRT6 2990/4885POLB 564/4885MAPT 415/4885

“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.