SCHEMBL3669544

SCHEMBL3669544

Cc1cc(Nc2nc(Cl)ncc2[N+](=O)[O-])n[nH]1

nearest known ligand 0.54

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ PIN1 Q13526 1/20 0.54
▸ PLK4 O00444 2/20 0.52
▸ PAK4 O96013 2/20 0.52
▸ MEN1 O00255 1/20 0.50
▸ HTT P42858 1/20 0.50
▸ KMT2A Q03164 1/20 0.50
▸ HSD17B10 Q99714 1/20 0.50
▸ AURKA O14965 6/20 0.48
▸ AURKB Q96GD4 4/20 0.48
▸ PIK3C3 Q8NEB9 5/20 0.47
▸ GSK3B P49841 1/20 0.47
▸ IGF1R P08069 3/20 0.47
▸ JAK2 O60674 3/20 0.40
▸ FGFR1 P11362 2/20 0.40
▸ NTRK1 P04629 2/20 0.40
▸ JAK3 P52333 2/20 0.40
▸ STK10 O94804 1/20 0.40
▸ RET P07949 1/20 0.40
▸ FER P16591 1/20 0.40
▸ CSNK2A2 P19784 1/20 0.40

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
SCHEMBL3719662 0.82 AURKA (0.53) PLK4PAK4MEN1HTTKMT2A
SCHEMBL56940 0.82 PIN1 (0.48) PIN1PLK4PAK4PIK3C3GSK3B
SCHEMBL56620 0.81 IGF1R (0.69) PIN1PIK3C3IGF1RNTRK1
SCHEMBL218642 0.80 MEN1 (0.62) PLK4PAK4MEN1HTTKMT2A
SCHEMBL218565 0.80 PAK4 (0.60) PLK4PAK4MEN1HTTKMT2A
SCHEMBL219315 0.78 PLK4 (0.58) PLK4PAK4MEN1HTTKMT2A
SCHEMBL219273 0.78 IGF1R (0.62) PLK4PAK4MEN1HTTKMT2A
SCHEMBL801630 0.76 IGF1R (0.46) PLK4PAK4AURKAAURKBIGF1R
SCHEMBL3663349 0.76 AURKA (0.49) PLK4PAK4MEN1HTTKMT2A
SCHEMBL8298042 0.75 PIN1 (0.58) PIN1MEN1KMT2AGSK3BPTK2B

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 10 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9221798-B2 4-substituted-(3-substituted-1H-pyrazole-5-amino)-pyrimidine derivatives having activity of inhibiting protein kinase and use thereof Zhejian Hisun Pharmaceutical Co., Ltd. (CN) 2015-12-29 — — US disclosed
US-9221798-B2 4-substituted-(3-substituted-1H-pyrazole-5-amino)-pyrimidine derivatives having activity of inhibiting protein kinase and use thereof Zhejian Hisun Pharmaceutical Co., Ltd. (CN) 2015-12-29 — — US disclosed
US-20150011545-A1 Chemical Compounds - 759 ASTRAZENECA AB (SE) 2015-01-08 — — US disclosed
US-20140378488-A1 4-SUBSTITUTED-(3-SUBSTITUTED-1H-PYRAZOLE-5-AMINO)-PYRIMIDINE DERIVATIVES HAVING ACTIVITY OF INHIBITING PROTEIN KINASE AND USE THEREOF ZHEJIANG HISUN PHARMACEUTICAL CO., LTD. (CN) 2014-12-25 — — US disclosed
US-20140378488-A1 4-SUBSTITUTED-(3-SUBSTITUTED-1H-PYRAZOLE-5-AMINO)-PYRIMIDINE DERIVATIVES HAVING ACTIVITY OF INHIBITING PROTEIN KINASE AND USE THEREOF ZHEJIANG HISUN PHARMACEUTICAL CO., LTD. (CN) 2014-12-25 — — US disclosed
US-20140155394-A1 Chemical Compounds - 759 ASTRAZENECA AB (SE) 2014-06-05 — — US disclosed
US-8486966-B2 9-(pyrazol-3-yl)-9H-purine-2-amine and 3-(pyrazol-3-yl) -3H-imidazo[4,5-B] pyridin-5-amine derivatives and their use for the treatment of cancer ASTRAZENECA AB (SE) 2013-07-16 — — US disclosed
US-20100324040-A1 9-(PYRAZOL-3-YL)-9H-PURINE-2-AMINE AND 3-(PYRAZOL-3-YL) -3H-IMIDAZO[4,5-B] PYRIDIN-5- AMINE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF CANCER ASTRAZENECA AB 2010-12-23 — — US disclosed
EP-2152705-A1 9- (PYRAZOL- 3 -YL) - 9H- PURINE-2 -AMINE AND 3- (PYRAZ0L-3-YL) -3H-IMIDAZ0 [4, 5-B]PYRIDIN-5-AMINE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF CANCER AstraZeneca AB (SE) 2010-02-17 — — EP disclosed
WO-2008135785-A1 9- (PYRAZOL- 3 -YL) - 9H- PURINE-2 -AMINE AND 3- (PYRAZ0L-3-YL) -3H-IMIDAZ0 [4, 5-B] PYRIDIN-5-AMINE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF CANCER ASTRAZENECA AB (SE) 2008-11-13 — — 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-20140378488-A1 4-SUBSTITUTED-(3-SUBSTITUTED-1H-PYRAZOLE-5-AMINO)-PYRIMIDINE DERIVATIVES HAVING ACTIVITY OF INHIBITING PROTEIN KINASE AND USE THEREOF MAP4K2, MAP4K1, MAP4K3 PIN1 2520/4885PLK4 388/4885PAK4 175/4885
US-20150011545-A1 Chemical Compounds - 759 MCL1, BCL9, BCL9L PIN1 1521/4885PLK4 1850/4885PAK4 1706/4885
US-20140155394-A1 Chemical Compounds - 759 MCL1, BCL9, BCL9L PIN1 1521/4885PLK4 1850/4885PAK4 1706/4885
US-20100324040-A1 9-(PYRAZOL-3-YL)-9H-PURINE-2-AMINE AND 3-(PYRAZOL-3-YL) -3H-IMIDAZO[4,5-B] PYRIDIN-5- AMINE DERIVATIVES AND THEIR USE FOR THE TREATMENT OF CANCER THPO, MPL, MCL1 PIN1 3173/4885PLK4 344/4885PAK4 883/4885

“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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