Semaxanib

Semaxanib

SCHEMBL19572

Cc1cc(C)c(C=C2C(=O)Nc3ccccc32)[nH]1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

FLT1FLT4KDRKIT

The experimentally established mechanism targets of Semaxanib. 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 6/20 1.00
FLT1 known ✓ P17948 3/20 1.00
FLT4 known ✓ P35916 2/20 1.00
KIT known ✓ P10721 1/20 1.00
RET P07949 7/20 1.00
ALK Q9UM73 5/20 1.00
FLT3 P36888 3/20 1.00
PDGFRB P09619 3/20 1.00
CSF1R P07333 2/20 1.00
FGFR1 P11362 2/20 1.00
SRC P12931 2/20 1.00
FGFR3 P22607 2/20 1.00
MAPK1 P28482 2/20 1.00
PDPK1 O15530 2/20 1.00
MEN1 O00255 1/20 1.00
NPC1 O15118 1/20 1.00
GMNN O75496 1/20 1.00
USP2 O75604 1/20 1.00
ABL1 P00519 1/20 1.00
LMNA P02545 1/20 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
Semaxanib SCHEMBL19571 1.00 RET (1.00) RETKDRALKFLT3FLT1
Semaxanib SCHEMBL29373311 1.00 RET (1.00) RETKDRALKFLT3FLT1
Semaxanib SCHEMBL29351025 1.00 RET (1.00) RETKDRALKFLT3FLT1
Semaxanib SCHEMBL28266617 1.00 RET (1.00) RETKDRALKFLT3FLT1
SCHEMBL32676579 0.87 RET (0.77) RETKDRALKFLT3FLT1
SCHEMBL32676595 0.87 RET (0.77) RETKDRALKFLT3FLT1
SCHEMBL32676489 0.87 RET (0.77) RETKDRALKFLT3FLT1
SCHEMBL5200799 0.85 KDR (0.74) RETKDRALKFLT3FLT1
SCHEMBL5200796 0.85 KDR (0.74) RETKDRALKFLT3FLT1
SCHEMBL8211131 0.84 RET (0.73) RETKDRALKFLT3FLT1

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 2000 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
CN-115298198-A Novel compounds and compositions for targeted therapy of kidney-related cancers 上海盟科药业股份有限公司 2022-11-04 CN claimed
EP-2805945-B1 Amide substituted indazoles as poly(ADP-ribose)polymerase (PARP) inhibitors MSD ITALIA SRL (IT) 2019-04-03 EP claimed
US-20170172989-A1 TREATMENT OF CANCERS HAVING RESISTANCE TO CHEMOTHERAPEUTIC AGENTS BAYER HEALTHCARE LLC (US) 2017-06-22 US claimed
US-20140301976-A1 NOVEL HYDROXAMATES AS THERAPEUTIC AGENTS PHARMACYCLICS, INC. 2014-10-09 US claimed
US-8779171-B2 Hydroxamates as therapeutic agents PHARMACYCLICS, INC. (US) 2014-07-15 US claimed
US-20130142758-A1 NOVEL HYDROXAMATES AS THERAPEUTIC AGENTS PHARMACYCLICS, INC. (US) 2013-06-06 US claimed
EP-1014953-B1 FORMULATIONS FOR HYDROPHOBIC PHARMACEUTICAL AGENTS SUGEN INC (US) 2012-04-25 EP claimed
EP-2425830-A1 Synergistic drug combination for the treatment of cancer Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. (DE) 2012-03-07 EP claimed
US-20110293615-A1 Use of Combination of Anti-Angiogenic Substance and c-kit Kinase Inhibitor EISAI R&D MANAGEMENT CO., LTD. (JP) 2011-12-01 US claimed
US-20020119198-A1 Self-emulsifying drug delivery systems for extremely water-insoluble, lipophilic drugs PHARMACIA & UPJOHN COMPANY 2002-08-29 US claimed
WO-2002064160-A2 PHARMACEUTICAL COMPOSITIONS WHICH INHIBIT VASCULAR PROLIFERATION AND METHOD OF USE THEREOF SOCIETE DE CONSEILS DE RECHERCHES ET D'APPLICATIONS SCIENTIFIQUES, S.A.S. (FR) 2002-08-22 WO claimed
WO-2002020020-A1 EXEMESTANE AS CHEMOPREVENTING AGENT PHARMACIA ITALIA S.P.A. (IT) 2002-03-14 WO claimed
US-20010012844-A1 Formulations for hydrophobic pharmaceutical agents SHENOY NARMADA (US) 2001-08-09 US claimed
WO-2001049287-A1 3-HETEROARYLIDENYL-2-INDOLINONE COMPOUNDS FOR MODULATING PROTEIN KINASE ACTIVITY AND FOR USE IN CANCER CHEMOTHERAPY SUGEN, INC. (US) 2001-07-12 WO claimed
US-6248771-B1 MIXTURE CONTAINING SURFACTANT; ANTIPROLIFERATIVE AGENTS; KINASE INHIBITOR SUGEN, INC. 2001-06-19 US claimed
EP-0769947-B1 INDOLINONE COMPOUNDS FOR THE TREATMENT OF DISEASE SUGEN INC (US) 2001-05-02 EP claimed
EP-1014953-A2 FORMULATIONS FOR HYDROPHOBIC PHARMACEUTICAL AGENTS Sugen, Inc. (US) 2000-07-05 EP claimed
WO-1998038984-A2 FORMULATIONS FOR HYDROPHOBIC PHARMACEUTICAL AGENTS SUGEN, INC. (US) 1998-09-11 WO claimed
US-5792783-A CAPABLE OF MODULATING TYROSINE KINASE SIGNAL TRANSDUCTION IN ORDER TO REGULATE, MODULATE AND/OR INHIBIT ABNORMAL CELL PROLIFERATION SUGEN, INC. (US) 1998-08-11 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 (7 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-20010012844-A1 Formulations for hydrophobic pharmaceutical agents ABCG2, SLC7A5, SLCO4C1 KDR 2394/4885FLT1 2324/4885FLT4 1918/4885
US-20130142758-A1 NOVEL HYDROXAMATES AS THERAPEUTIC AGENTS HDAC1, HDAC3, HDAC5 KDR 4789/4885FLT1 4806/4885FLT4 4688/4885
US-20140301976-A1 NOVEL HYDROXAMATES AS THERAPEUTIC AGENTS HDAC1, HDAC3, HDAC5 KDR 4789/4885FLT1 4806/4885FLT4 4688/4885
US-20170172989-A1 TREATMENT OF CANCERS HAVING RESISTANCE TO CHEMOTHERAPEUTIC AGENTS CDK4, TP53, ABCC1 KDR 2076/4885FLT1 1335/4885FLT4 1122/4885
US-20020119198-A1 Self-emulsifying drug delivery systems for extremely water-insoluble, lipophilic drugs LIPA, ABCG2, LIPG KDR 1068/4885FLT1 1797/4885FLT4 1708/4885
US-20110293615-A1 Use of Combination of Anti-Angiogenic Substance and c-kit Kinase Inhibitor KIT, FLT4, KDR KDR 3/4885FLT1 5/4885FLT4 2/4885
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.