SCHEMBL589205

SCHEMBL589205

Cc1c2ccc(N(C)c3ccnc(Cl)n3)cc2nn1C

nearest known ligand 0.68

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR P35968 16/20 0.68
KIT P10721 9/20 0.68
PDGFRA P16234 9/20 0.68
HDAC1 Q13547 4/20 0.56
HDAC6 Q9UBN7 4/20 0.56
HDAC3 O15379 2/20 0.56
HDAC4 P56524 2/20 0.56
HDAC7 Q8WUI4 2/20 0.56
HDAC2 Q92769 2/20 0.56
HDAC10 Q969S8 2/20 0.56
HDAC11 Q96DB2 2/20 0.56
HDAC8 Q9BY41 2/20 0.56
HDAC9 Q9UKV0 2/20 0.56
HDAC5 Q9UQL6 2/20 0.56
FLT1 P17948 3/20 0.56
ABCB11 O95342 2/20 0.56
CYP3A4 P08684 2/20 0.56
CYP2D6 P10635 2/20 0.56
CYP2C9 P11712 2/20 0.56
CYP2C19 P33261 2/20 0.56

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
SCHEMBL1961077 0.92 KDR (0.60) KDRKITPDGFRAHDAC1HDAC6
SCHEMBL23587599 0.90 KDR (0.56) KDRKITPDGFRAHDAC1HDAC6
SCHEMBL18101235 0.89 KDR (0.56) KDRKITPDGFRAHDAC1HDAC6
SCHEMBL14347685 0.88 KDR (0.67) KDRKITPDGFRAHDAC1HDAC6
SCHEMBL29516846 0.88 KDR (0.67) KDRKITPDGFRAHDAC1HDAC6
Hydrochloric Acid SCHEMBL29516748 0.86 KDR (0.66) KDRKITPDGFRAHDAC1HDAC6
SCHEMBL11953494 0.86 KDR (0.66) KDRKITPDGFRAHDAC1HDAC6
SCHEMBL13849112 0.85 KDR (0.65) KDRKITPDGFRAHDAC1HDAC6
SCHEMBL20729864 0.85 KDR (0.65) KDRKITPDGFRAHDAC1HDAC6
Hydrochloric Acid SCHEMBL30817650 0.84 KDR (0.64) KDRKITPDGFRAHDAC1HDAC6

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117169410-A Method for analyzing indazole structure related substances 南京正大天晴制药有限公司 2023-12-05 CN claimed
CN-116242934-A Detection method and application of related substances of pezopanib hydrochloride intermediate PZP-M2 山西振东制药股份有限公司 2023-06-09 CN claimed
US-11299477-B2 Process for the preparation of Pazopanib or a pharmaceutically acceptable salt thereof LAURUS LABS LIMITED (IN) 2022-04-12 US claimed
CN-109212042-B Analysis method for determining toxicity impurities of pezopyr hydrochloride gene by adopting liquid chromatography-mass spectrometry 齐鲁制药有限公司 2022-03-04 CN claimed
WO-2020238220-A1 METHOD FOR PREPARING PAZOPANIB HYDROCHLORIDE 济南爱思医药科技有限公司 2020-12-03 WO claimed
CN-110143951-B Synthetic method of pazopanib hydrochloride raw material trimer impurity 博诺康源(北京)药业科技有限公司 2020-11-10 CN claimed
US-20200262821-A1 PROCESS FOR THE PREPARATION OF PAZOPANIB OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF LAURUS LABS LIMITED (IN) 2020-08-20 US claimed
US-10626110-B2 Polymorph of pazopanib hydrochloride and preparation process thereof FORMOSA LABORATORIES, INC. (TW) 2020-04-21 US claimed
US-20200048224-A1 NOVEL POLYMORPH OF PAZOPANIB HYDROCHLORIDE AND PREPARATION PROCESS THEREOF FORMOSA LABORATORIES, INC. (TW) 2020-02-13 US claimed
CN-110028495-B The preparation method of pazopanib hydrochloride 济南爱思医药科技有限公司 2019-12-03 CN claimed
CN-110143951-A Synthetic method of pazopanib hydrochloride raw material trimer impurity 博诺康源(北京)药业科技有限公司 2019-08-20 CN claimed
CN-110028495-A The environment-friendly preparation method thereof of pazopanib hydrochloride 济南爱思医药科技有限公司 2019-07-19 CN claimed
US-20160280689-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF PAZOPANIB OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF LAURUS LABS LIMITED (IN) 2016-09-29 US claimed
US-20240050429-A1 PAZOPANIB PHARMACEUTICAL COMPOSITION, INJECTION AND PREPARATION METHOD AND USE THEREOF Qx Therapeutics, Inc. 2024-02-15 US disclosed
CN-117510513-A Heterocyclic compounds having biological activity 首药控股(北京)股份有限公司 2024-02-06 CN disclosed
CN-117169410-A Method for analyzing indazole structure related substances 南京正大天晴制药有限公司 2023-12-05 CN disclosed
WO-2005105094-A2 CANCER TREATMENT METHOD SMITHKLINE BEECHAM CORPORATION (US) 2005-11-10 WO disclosed
EP-1515955-A2 CHEMICAL PROCESS SmithKline Beecham Corporation (US) 2005-03-23 EP disclosed
US-20040242578-A1 Pyrimidineamines as angiogenesis modulators NOVARTIS AG (CH) 2004-12-02 US disclosed
WO-2003106416-A2 CHEMICAL PROCESS SMITHKLINE BEECHAM CORPORATION (US) 2003-12-24 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 (6 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-20040242578-A1 Pyrimidineamines as angiogenesis modulators TYMS, TYMP, DPYD KDR 5/4885KIT 183/4885PDGFRA 13/4885
US-11299477-B2 Process for the preparation of Pazopanib or a pharmaceutically acceptable salt thereof JAK2, SF3B5, PDGFRB KDR 19/4885KIT 1154/4885PDGFRA 5/4885
US-10626110-B2 Polymorph of pazopanib hydrochloride and preparation process thereof PDGFRB, PDGFRA, PNP KDR 5/4885KIT 882/4885PDGFRA 2/4885
US-20160280689-A1 AN IMPROVED PROCESS FOR THE PREPARATION OF PAZOPANIB OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF SF3B5, PDGFRB, JAK2 KDR 10/4885KIT 1459/4885PDGFRA 4/4885
US-20200048224-A1 NOVEL POLYMORPH OF PAZOPANIB HYDROCHLORIDE AND PREPARATION PROCESS THEREOF PDGFRB, KDR, PDGFRA KDR 2/4885KIT 629/4885PDGFRA 3/4885
US-20200262821-A1 PROCESS FOR THE PREPARATION OF PAZOPANIB OR A PHARMACEUTICALLY ACCEPTABLE SALT THEREOF JAK2, SF3B5, PDGFRB KDR 18/4885KIT 1039/4885PDGFRA 5/4885

“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.