SCHEMBL4765653

SCHEMBL4765653

CCOC(=O)c1ccc(-c2cc3c(Cl)ncnc3[nH]2)cc1

nearest known ligand 0.49

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CSF1R P07333 4/20 0.49
GCGR P47871 2/20 0.46
MAPK14 Q16539 1/20 0.46
TUBB4A P04350 1/20 0.45
TUBB P07437 1/20 0.45
TUBA3C P0DPH7 1/20 0.45
TUBA1B P68363 1/20 0.45
TUBA4A P68366 1/20 0.45
TUBB4B P68371 1/20 0.45
TUBB3 Q13509 1/20 0.45
TUBB2A Q13885 1/20 0.45
TUBB8 Q3ZCM7 1/20 0.45
TUBA3E Q6PEY2 1/20 0.45
TUBA1A Q71U36 1/20 0.45
TUBA1C Q9BQE3 1/20 0.45
TUBB6 Q9BUF5 1/20 0.45
TUBB2B Q9BVA1 1/20 0.45
TUBB1 Q9H4B7 1/20 0.45
SIRT2 Q8IXJ6 1/20 0.44
SIRT1 Q96EB6 1/20 0.44

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
SCHEMBL4901729 0.88 CSF1R (0.55) CSF1REGFRKDM4EALDH1A1HDAC3
SCHEMBL7492031 0.88 CSF1R (0.53) CSF1RTUBB4ATUBBTUBA3CTUBA1B
SCHEMBL7491418 0.87 CSF1R (0.50) CSF1RGCGRMAPK14TUBB4ATUBB
SCHEMBL13604156 0.84 CSF1R (0.60) CSF1REGFR
SCHEMBL4071289 0.81 EGFR (0.58) CSF1REGFRHDAC3KDRHDAC4
SCHEMBL4764786 0.81 LMNA (0.56) CSF1REGFRKDM4EALDH1A1HPGD
Hydrochloric Acid SCHEMBL2747959 0.81 SIRT2 (0.46) GCGRMAPK14TUBB4ATUBBTUBA3C
SCHEMBL20325470 0.80 KDR (0.55) CSF1REGFRKDM4EALDH1A1HDAC3
SCHEMBL4773160 0.80 ERBB2 (0.58) CSF1REGFRHDAC3KDRHDAC4
SCHEMBL4764369 0.80 EGFR (0.52) EGFRKDM4EALDH1A1HPGDERBB2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4166557-B1 INTERMEDIATES OF N-(3-(7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)PHENYL)BENZAMIDE DERIVATIVES NOVARTIS AG (CH) 2026-05-06 EP disclosed
US-12441733-B2 Substituted 2,4-dioxotetrahydropyrimidines as intermediates in the synthesis of bruton's tyrosine kinase inhibitors NOVARTIS AG (CH) 2025-10-14 US disclosed
EP-4467549-A2 INTERMEDIATES OF N-(3-(7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)PHENYL)BENZAMIDE DERIVATIVES Novartis AG (CH) 2024-11-27 EP disclosed
US-20240158399-A1 N-(3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)benzamide Derivatives NOVARTIS AG (CH) 2024-05-16 US disclosed
US-20230398117-A1 3-hydroxy-N-(3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)pyrrolidine-1-carboxamide Derivatives NOVARTIS AG (CH) 2023-12-14 US disclosed
EP-4166557-A1 INTERMEDIATES OF N-(3-(7H-PYRROLO[2,3-D]PYRIMIDIN-4-YL)PHENYL)BENZAMIDE DERIVATIVES Novartis AG (CH) 2023-04-19 EP disclosed
US-11613543-B2 Substituted pyrrolo[2,3-d]pyrimidines as Bruton's Tyrosine Kinase inhibitors NOVARTIS AG (CH) 2023-03-28 US disclosed
US-11541056-B2 3-hydroxy-N-(3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)pyrrolidine-1-carboxamide derivatives NOVARTIS AG (CH) 2023-01-03 US disclosed
US-20220387602-A1 BIFUNCTIONAL DEGRADERS AND THEIR METHODS OF USE NOVARTIS AG (CH) 2022-12-08 US disclosed
US-20210251996-A1 3-hydroxy-N-(3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)pyrrolidine-1-carboxamide Derivatives NOVARTIS AG (CH) 2021-08-19 US disclosed
US-20070135460-A1 7H-pyrrolopyrimidine derivatives CARAVATTI GIORGIO 2007-06-14 US disclosed
US-20050038048-A1 Use of 7h-pyrrollo{2,3-d}pyrimidine derivatives in the treatment of solid tumor diseases BALL HOWARD ASHLEY (US) 2005-02-17 US disclosed
US-20040248911-A1 7H-pyrrolo[2,3-d]pyrimidine derivatives BOLD GUIDO (CH) 2004-12-09 US disclosed
US-20040242600-A1 4-amino-6-phenyl-pyrrolo[2,3-d]pyrimidine derivatives NOVARTIS AG (CH) 2004-12-02 US disclosed
EP-1441736-A2 USE OF 7H-PYRROLO[2,3-D]PYRIMIDINE DERIVATIVES IN THE TREATMENT OF SOLID TUMOR DISEASES Novartis AG (CH) 2004-08-04 EP disclosed
WO-2003037897-A2 USE OF 7H-PYRROLO[2,3-D]PYRIMIDINE DERIVATIVES IN THE TREATMENT OF SOLID TUMOR DISEASES NOVARTIS AG (CH) 2003-05-08 WO disclosed
EP-0836605-B1 PYRROLOPYRIMIDINES AND PROCESSES FOR THE PREPARATION THEREOF NOVARTIS AG (CH) 2002-02-06 EP disclosed
US-6140332-A Pyrrolopyrimidines and processes for the preparation thereof NOVARTIS AG (CH) 2000-10-31 US disclosed
EP-0836605-A1 PYRROLOPYRIMIDINES AND PROCESSES FOR THE PREPARATION THEREOF Novartis AG (CH) 1998-04-22 EP disclosed
WO-1997002266-A1 PYRROLOPYRIMIDINES AND PROCESSES FOR THE PREPARATION THEREOF NOVARTIS AG (CH) 1997-01-23 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 (11 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-11541056-B2 3-hydroxy-N-(3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)pyrrolidine-1-carboxamide derivatives PAH, PKD1, REN CSF1R 2510/4885GCGR 1470/4885MAPK14 1521/4885
US-20240158399-A1 N-(3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)benzamide Derivatives PAH, REN, PKD1 CSF1R 2502/4885GCGR 1139/4885MAPK14 1262/4885
US-20050038048-A1 Use of 7h-pyrrollo{2,3-d}pyrimidine derivatives in the treatment of solid tumor diseases TYMS, DPYD, TYMP CSF1R 3226/4885GCGR 4368/4885MAPK14 2990/4885
US-20220387602-A1 BIFUNCTIONAL DEGRADERS AND THEIR METHODS OF USE JMJD7, MDM2, IDE CSF1R 2770/4885GCGR 2588/4885MAPK14 4473/4885
US-20230398117-A1 3-hydroxy-N-(3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)pyrrolidine-1-carboxamide Derivatives PAH, PKD1, REN CSF1R 2510/4885GCGR 1470/4885MAPK14 1521/4885
US-20210251996-A1 3-hydroxy-N-(3-(7H-pyrrolo[2,3-d]pyrimidin-4-yl)phenyl)pyrrolidine-1-carboxamide Derivatives PAH, PKD1, REN CSF1R 2510/4885GCGR 1470/4885MAPK14 1521/4885
US-20070135460-A1 7H-pyrrolopyrimidine derivatives DPYD, TYMP, DHPS CSF1R 3432/4885GCGR 3745/4885MAPK14 1877/4885
US-20040248911-A1 7H-pyrrolo[2,3-d]pyrimidine derivatives DPYD, DHPS, TYMP CSF1R 3024/4885GCGR 3842/4885MAPK14 2688/4885
US-12441733-B2 Substituted 2,4-dioxotetrahydropyrimidines as intermediates in the synthesis of bruton's tyrosine kinase inhibitors BTK, ABL1, LYN CSF1R 3845/4885GCGR 1826/4885MAPK14 366/4885
US-20040242600-A1 4-amino-6-phenyl-pyrrolo[2,3-d]pyrimidine derivatives DPYD, TYMP, TYMS CSF1R 3516/4885GCGR 3216/4885MAPK14 2452/4885
US-11613543-B2 Substituted pyrrolo[2,3-d]pyrimidines as Bruton's Tyrosine Kinase inhibitors BTK, ABL1, JAK1 CSF1R 2692/4885GCGR 3295/4885MAPK14 397/4885

“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.