Semaxanib

Semaxanib

SCHEMBL29373311

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 SCHEMBL19572 1.00 RET (1.00) RETKDRALKFLT3FLT1
Semaxanib SCHEMBL19571 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 25 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260000691-A1 COMPOUNDS, METHODS, AND TREATMENTS FOR ABNORMAL SIGNALING PATHWAYS FOR PRENATAL AND POSTNATAL DEVELOPMENT JENNINGS BARBARA BROOKE (US) 2026-01-01 US disclosed
WO-2025244963-A1 ECTEINASCIDIN DERIVATIVES AND METHODS OF USE THEREOF AS ANTITUMOR AGENTS MERCK SHARP & DOHME LLC (US) 2025-11-27 WO disclosed
EP-4630001-A1 SUBSTITUTED QUINAZOLINE DERIVATIVES AND METHODS OF USE THEREOF Merck Sharp & Dohme LLC (US) 2025-10-15 EP disclosed
EP-4608398-A1 PNU ANTHRACYCLINE DERIVATIVES AND METHODS OF USE THEREOF Merck Sharp & Dohme LLC (US) 2025-09-03 EP disclosed
WO-2025136841-A1 SUBSTITUTED ISOQUINOLINE DERIVATIVES AND METHODS OF USE THEREOF MERCK SHARP & DOHME LLC (US) 2025-06-26 WO disclosed
CN-119923398-A Cyclic compounds and methods of use thereof 薛定谔公司 2025-05-02 CN disclosed
US-20250136697-A1 METHODS AND COMPOSITIONS COMPRISING B7H3 CHIMERIC ANTIGEN RECEPTORS SEATTLE CHILDRENS HOSPITAL DBA SEATTLE CHILDRENS RES INST (US) 2025-05-01 US disclosed
US-12173071-B2 Methods and compositions comprising B7H3 chimeric antigen receptors SEATTLE CHILDREN'S HOSPITAL (US) 2024-12-24 US disclosed
CN-112805006-B PRMT5 inhibitors 默沙东有限责任公司 2024-09-24 CN disclosed
WO-2024123585-A1 SUBSTITUTED QUINAZOLINE DERIVATIVES AND METHODS OF USE THEREOF MERCK SHARP & DOHME LLC (US) 2024-06-13 WO disclosed
CN-115087638-A PRMT5 inhibitor 默沙东公司 2022-09-20 CN disclosed
CN-115003303-A PRMT5 inhibitor 默沙东公司 2022-09-02 CN disclosed
CN-106008460-B Pharmaceutically acceptable salts of 2- {4- [ (3S) -piperidin-3-yl ] phenyl } -2H-indazole-7-carboxamide 默沙东公司 2022-08-12 CN disclosed
CN-114761432-A Dosing regimen of anti-CD 27 antibodies for treatment of cancer 默沙东公司 2022-07-15 CN disclosed
CN-110272426-B Alkynyl (hetero) aromatic ring compounds for inhibiting protein kinase activity 深圳市塔吉瑞生物医药有限公司 2022-05-31 CN disclosed
WO-2022080473-A1 NERVE CELL ACTIVATOR 三沢幸子 2022-04-21 WO disclosed
EP-3982998-A1 COMPOSITIONS AND METHODS FOR SUBCUTANEOUS ADMINISTRATION OF CANCER IMMUNOTHERAPY Alkermes Pharma Ireland Limited (IE) 2022-04-20 EP disclosed
CN-110194772-B Alkynyl (hetero) aromatic ring compounds for inhibiting protein kinase activity 深圳市塔吉瑞生物医药有限公司 2022-04-05 CN disclosed
WO-2022046771-A1 JUVENILE PROTECTIVE FACTORS TO ARREST AND REVERSE AGING IN THE ENTERIC NERVOUS SYSTEM THE JOHNS HOPKINS UNIVERSITY (US) 2022-03-03 WO disclosed
CN-108289922-B Therapeutic methods and compositions for treating non-small cell lung cancer 友杏生技医药股份有限公司 2022-02-08 CN 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 (1 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-20260000691-A1 COMPOUNDS, METHODS, AND TREATMENTS FOR ABNORMAL SIGNALING PATHWAYS FOR PRENATAL AND POSTNATAL DEVELOPMENT PDK1, IP6K1, IP6K3 KDR 536/4885FLT1 741/4885FLT4 355/4885

“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.