Axitinib

Axitinib

SCHEMBL172918

CNC(=O)c1ccccc1Sc1ccc2c(/C=C/c3ccccn3)n[nH]c2c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

FLT1FLT4KDR

The experimentally established mechanism targets of Axitinib. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KDR known ✓ P35968 19/20 1.00
FLT1 known ✓ P17948 3/20 1.00
FLT4 known ✓ P35916 3/20 1.00
FGFR1 P11362 7/20 1.00
LCK P06239 3/20 1.00
PLK4 O00444 2/20 1.00
AURKA O14965 2/20 1.00
MAP4K4 O95819 2/20 1.00
PAK4 O96013 2/20 1.00
ABL1 P00519 2/20 1.00
CSF1R P07333 2/20 1.00
RET P07949 2/20 1.00
MET P08581 2/20 1.00
PDGFRB P09619 2/20 1.00
KIT P10721 2/20 1.00
PDGFRA P16234 2/20 1.00
FGFR3 P22607 2/20 1.00
TYK2 P29597 2/20 1.00
AXL P30530 2/20 1.00
BLK P51451 2/20 1.00

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
Axitinib SCHEMBL29384419 1.00 KDR (1.00) KDRFGFR1FLT1FLT4LCK
Axitinib SCHEMBL843204 1.00 KDR (1.00) KDRFGFR1FLT1FLT4LCK
Axitinib SCHEMBL29349703 1.00 KDR (1.00) KDRFGFR1FLT1FLT4LCK
Axitinib SCHEMBL2826667 1.00 KDR (1.00) KDRFGFR1FLT1FLT4LCK
Axitinib SCHEMBL29387511 1.00 KDR (1.00) KDRFGFR1FLT1FLT4LCK
Axitinib SCHEMBL5248175 0.99 KDR (0.98) KDRFGFR1FLT1FLT4LCK
Axitinib SCHEMBL5248178 0.99 KDR (0.98) KDRFGFR1FLT1FLT4LCK
Axitinib SCHEMBL23044964 0.94 KDR (0.88) KDRFGFR1FLT1FLT4LCK
Axitinib SCHEMBL29459456 0.94 KDR (0.88) KDRFGFR1FLT1FLT4LCK
SCHEMBL24503457 0.91 KDR (0.84) KDRFGFR1FLT1FLT4LCK

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20240252454-A1 COMPOSITION COMPRISING AN INHIBITOR OF MITOCHONDRIAL TRANSCRIPTION LEAD DISCOVERY CENTER GMBH (DE) 2024-08-01 US claimed
CN-118286440-A Combination of PD-1 antagonists and VEGFR inhibitors for the treatment of cancer 辉瑞大药厂 2024-07-05 CN claimed
EP-4333822-A1 COMPOSITION COMPRISING AN INHIBITOR OF MITOCHONDRIAL TRANSCRIPTION Lead Discovery Center GmbH (DE) 2024-03-13 EP claimed
EP-4249063-A2 CRYSTALLINE FORMS OF 6-[2-(METHYLCARBAMOYL)PHENYLSULFANYL]-3-E-[2-(PYRIDIN-2-YL)ETHENYL]INDAZOLE SUITABLE FOR THE TREATMENT OF ABNORMAL CELL GROWTH IN MAMMALS Pfizer Products Inc. (US) 2023-09-27 EP claimed
EP-2134702-B2 CRYSTALLINE FORMS OF 6-[2-(METHYLCARBAMOYL)PHENYLSULFANYL]-3-E-[2-(PYRIDIN-2-YL)ETHENYL]INDAZOLE SUITABLE FOR THE TREATMENT OF ABNORMAL CELL GROWTH IN MAMMALS PFIZER PROD INC (US) 2023-08-30 EP claimed
US-20230141981-A1 NOVEL COMPOUNDS AND COMPOSITION FOR TARGETED THERAPY OF KIDNEY-ASSOCIATED CANCERS Shanghai MICURX Pharmaceuticals Co., Ltd. (CN) 2023-05-11 US claimed
WO-2022233782-A1 COMPOSITION COMPRISING AN INHIBITOR OF MITOCHONDRIAL TRANSCRIPTION LEAD DISCOVERY CENTER GMBH (DE) 2022-11-10 WO claimed
EP-3252047-B1 CRYSTALLINE FORMS OF 6-[2-(METHYLCARBAMOYL)PHENYLSULFANYL]-3-E-[2-(PYRIDIN-2-YL)ETHENYL]INDAZOLE SUITABLE FOR THE TREATMENT OF ABNORMAL CELL GROWTH IN MAMMALS PFIZER PROD INC (US) 2022-05-11 EP claimed
EP-3971209-A1 COMBINATION OF A PD-1 ANTAGONIST AND A VEGFR INHIBITOR FOR TREATING CANCER Pfizer Inc. (US) 2022-03-23 EP claimed
CN-107750166-B PD-L1 antagonist combination therapy 默克专利股份有限公司 2022-02-11 CN claimed
EP-1949902-A1 USE OF COMBINATION OF ANTI-ANGIOGENIC SUBSTANCE AND c-kit KINASE INHIBITOR Eisai R&D Management Co., Ltd. (JP) 2008-07-30 EP claimed
EP-1925676-A1 METHOD FOR ASSAY ON THE EFFECT OF VASCULARIZATION INHIBITOR Eisai R&D Management Co., Ltd. (JP) 2008-05-28 EP claimed
EP-1925941-A1 METHOD FOR PREDICTION OF THE EFFICACY OF VASCULARIZATION INHIBITOR Eisai R&D Management Co., Ltd. (JP) 2008-05-28 EP claimed
EP-1885338-A1 PHARMACEUTICAL COMPOSTIONS COMPRISING AN AMORPHOUS FORM OF A VEGF-R INHIBITOR Pfizer, Inc. (US) 2008-02-13 EP claimed
EP-1819696-A1 POLYMORPHIC FORMS OF 6-2-(METHYLCARBAMOYL)PHENYSULFANYL|-3-E-2-(PYRIDIN-2-YL)ETHENYL INDAZOLE Pfizer, Inc. (US) 2007-08-22 EP claimed
EP-1797877-A1 JOINT USE OF SULFONAMIDE BASED COMPOUND WITH ANGIOGENESIS INHIBITOR Eisai Co., Ltd. (JP) 2007-06-20 EP claimed
WO-2006123223-A1 PHARMACEUTICAL COMPOSTIONS COMPRISING AN AMORPHOUS FORM OF A VEGF-R INHIBITOR PFIZER INC. (US) 2006-11-23 WO claimed
US-20060135486-A1 Use of sulfonamide-including compounds in combination with angiogenesis inhibitors EISAI CO., LTD. (JP) 2006-06-22 US claimed
WO-2006048751-A1 POLYMORPHIC FORMS OF 6-[2-(METHYLCARBAMOYL)PHENYLSULFANYL]-3-E-[2-(PYRIDIN-2-YL)ETHENYL]INDAZOLE PFIZER INC. (US) 2006-05-11 WO claimed
US-20060094763-A1 Polymorphic forms of 6-[2-(methylcarbomoyl) phenyl sulfanyl]-3-E-[2-(pyridin-2-yl)ethenyl]indazole AGOURON PHARMACEUTICALS, INC. 2006-05-04 US claimed

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-20060135486-A1 Use of sulfonamide-including compounds in combination with angiogenesis inhibitors FLT4, KDR, FLT1 KDR 2/4885FLT1 3/4885FLT4 1/4885
US-20060094763-A1 Polymorphic forms of 6-[2-(methylcarbomoyl) phenyl sulfanyl]-3-E-[2-(pyridin-2-yl)ethenyl]indazole BRCA1, CSNK1G3, PRKACB KDR 3044/4885FLT1 3957/4885FLT4 3174/4885
US-20240252454-A1 COMPOSITION COMPRISING AN INHIBITOR OF MITOCHONDRIAL TRANSCRIPTION TFAM, POLRMT, TUFM KDR 3850/4885FLT1 3446/4885FLT4 3252/4885
US-20230141981-A1 NOVEL COMPOUNDS AND COMPOSITION FOR TARGETED THERAPY OF KIDNEY-ASSOCIATED CANCERS GLS, ATP6V1B1, KRAS KDR 277/4885FLT1 326/4885FLT4 209/4885

“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.