Lestaurtinib

Lestaurtinib

SCHEMBL1649693

C[C@]12OC(C[C@]1(O)CO)n1c3ccccc3c3c4c(c5c6ccccc6n2c5c31)CNC4=O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

FLT3JAK2NTRK1NTRK2NTRK3RET

The experimentally established mechanism targets of Lestaurtinib. 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
NTRK1 known ✓ P04629 10/20 1.00
FLT3 known ✓ P36888 5/20 1.00
JAK2 known ✓ O60674 2/20 1.00
RET known ✓ P07949 2/20 1.00
NTRK3 known ✓ Q16288 1/20 1.00
NTRK2 known ✓ Q16620 1/20 1.00
KDR P35968 9/20 1.00
PRKCQ Q04759 7/20 1.00
PRKD3 O94806 5/20 1.00
PRKCA P17252 5/20 1.00
PRKCH P24723 5/20 1.00
PRKCI P41743 5/20 1.00
PRKCE Q02156 5/20 1.00
PRKCD Q05655 5/20 1.00
PRKD1 Q15139 5/20 1.00
MYLK Q15746 4/20 1.00
CDK4 P11802 3/20 1.00
CDK2 P24941 3/20 1.00
MAP3K11 Q16584 3/20 1.00
CAMKK2 Q96RR4 3/20 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
Lestaurtinib SCHEMBL16139562 1.00 NTRK1 (1.00) NTRK1KDRPRKCQFLT3PRKD3
Lestaurtinib SCHEMBL730955 1.00 NTRK1 (1.00) NTRK1KDRPRKCQFLT3PRKD3
Lestaurtinib SCHEMBL12228516 1.00 NTRK1 (1.00) NTRK1KDRPRKCQFLT3PRKD3
Lestaurtinib SCHEMBL29625224 1.00 NTRK1 (1.00) NTRK1KDRPRKCQFLT3PRKD3
Lestaurtinib SCHEMBL17971367 1.00 NTRK1 (1.00) NTRK1KDRPRKCQFLT3PRKD3
Lestaurtinib SCHEMBL17971365 1.00 NTRK1 (1.00) NTRK1KDRPRKCQFLT3PRKD3
Lestaurtinib SCHEMBL12963759 1.00 NTRK1 (1.00) NTRK1KDRPRKCQFLT3PRKD3
Lestaurtinib SCHEMBL13169434 1.00 NTRK1 (1.00) NTRK1KDRPRKCQFLT3PRKD3
Lestaurtinib SCHEMBL30149252 0.99 NTRK1 (0.98) NTRK1KDRPRKCQFLT3PRKD3
SCHEMBL14342269 0.94 NTRK1 (0.89) NTRK1KDRPRKCQFLT3PRKD3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4378957-A2 COMBINATION THERAPIES COMPRISING ANTIBODY MOLECULES TO PD-1 Novartis AG (CH) 2024-06-05 EP claimed
CN-110882294-A Pharmaceutical composition for relieving and/or treating inflammatory pain 西安跃亿智产信息科技有限公司 2020-03-17 CN claimed
EP-2635299-B1 METHODS FOR TREATING HAIR LOSS DISORDERS UNIV COLUMBIA (US) 2019-07-31 EP claimed
EP-3325504-B1 METHODS FOR IMPROVING THE EFFICACY AND EXPANSION OF IMMUNE CELLS NOVARTIS AG (CH) 2026-05-27 EP disclosed
EP-3523331-B1 CHIMERIC ANTIGEN RECEPTORS FOR THE TREATMENT OF CANCER NOVARTIS AG (CH) 2026-05-27 EP disclosed
US-12594321-B2 Bispecific chimeric antigen receptor that binds CD19 and CD20, encoding nucleic acid molecules thereof and methods of use thereof to treat cancer NOVARTIS AG (CH) 2026-04-07 US disclosed
US-12527818-B2 Platinum-based chemotherapy, mast binding agents, glucocorticoid receptor (GR) binding agents, and/or HSP90 binding agents for uses in treating cancer EMORY UNIVERSITY (US) 2026-01-20 US disclosed
US-20250333480-A1 FUSION MOLECULES AND USES THEREOF FOUNDATION MEDICINE, INC. (US) 2025-10-30 US disclosed
US-20250333479-A1 NOVEL FUSION MOLECULES AND USES THEREOF FOUNDATION MEDICINE, INC. (US) 2025-10-30 US disclosed
US-12391946-B2 Use of a Janus kinase inhibitor and a telomerase inhibitor for the treatment of myeloproliferative neoplasms GERON CORPORATION (US) 2025-08-19 US disclosed
US-20250249112-A1 MACROPINOCYTOSIS SELECTIVE NON-BINDING PROTEIN-DRUG CONJUGATES TEZCAT BIOSCIENCES, INC. 2025-08-07 US disclosed
WO-2008013782-A2 METHODS FOR PROMOTING MYELINATION, NEURONAL SURVIVAL AND OLIGODENDROCYTE DIFFERENTIATION VIA ADMINISTRATION OF SP35 OR TRKA ANTAGONISTS BIOGEN IDEC MA INC. (US) 2008-01-31 WO disclosed
US-20080021013-A1 JAK inhibitors for treatment of myeloproliferative disorders CEPHALON, INC. (US) 2008-01-24 US disclosed
US-20080021013-A1 JAK inhibitors for treatment of myeloproliferative disorders CEPHALON, INC. (US) 2008-01-24 US disclosed
US-20070281907-A1 Kinase Inhibitor Phosphonate Conjugates GILEAD SCIENCES, INC. 2007-12-06 US disclosed
US-20070281907-A1 Kinase Inhibitor Phosphonate Conjugates GILEAD SCIENCES, INC. 2007-12-06 US disclosed
WO-2007075307-A2 CRYSTALLINE LESTAURTINIB HYDRATES AND CRYSTALLINE LESTAURTINIB HEMIHYDRATE HEMIACETONITRILEATE AND CRYSTALLINE LESTAURTINIB HEMIHYDRATE HEMITETRAHYDROFURANATE ABBOTT LABORATORIES (US) 2007-07-05 WO disclosed
WO-2007070444-A1 LESTAURTINIB CRYSTALLINE FORM 1, CRYSTALLINE LESTAURIMIB ANHYDRATE AND AMORPHOUS LESTAURIMIB ABBOTT LABORATORIES (US) 2007-06-21 WO disclosed
US-20070135401-A1 Lestaurtinib Crystalline Form 1, crystalline lestaurimib anhydrate and amorphous lestaurimib ABBOTT LABORATORIES 2007-06-14 US disclosed
US-20070135628-A1 Crystalline lestaurtinib hydrates and crystalline lestaurtinib hemihydrate hemiacetonitrileate and crystalline lestaurtinib hemihydrate hemitetrahydrofuranate ABBOTT LABORATORIES 2007-06-14 US 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 (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-12594321-B2 Bispecific chimeric antigen receptor that binds CD19 and CD20, encoding nucleic acid molecules thereof and methods of use thereof to treat cancer CD2, CD22, KLRK1 NTRK1 319/4885FLT3 107/4885JAK2 798/4885
US-12527818-B2 Platinum-based chemotherapy, mast binding agents, glucocorticoid receptor (GR) binding agents, and/or HSP90 binding agents for uses in treating cancer HSP90AB1, HSP90B1, MAST1 NTRK1 694/4885FLT3 759/4885JAK2 520/4885
US-20080021013-A1 JAK inhibitors for treatment of myeloproliferative disorders JAK2, JAK3, JAK1 NTRK1 3652/4885FLT3 17/4885JAK2 1/4885
US-20250333479-A1 NOVEL FUSION MOLECULES AND USES THEREOF RPS27A, CD2BP2, FGB NTRK1 1066/4885FLT3 548/4885JAK2 2701/4885
US-12391946-B2 Use of a Janus kinase inhibitor and a telomerase inhibitor for the treatment of myeloproliferative neoplasms TERT, JAK2, MCL1 NTRK1 2857/4885FLT3 106/4885JAK2 2/4885
US-20250333480-A1 FUSION MOLECULES AND USES THEREOF RPS27A, CD2BP2, FGB NTRK1 1138/4885FLT3 441/4885JAK2 2272/4885
US-20070281907-A1 Kinase Inhibitor Phosphonate Conjugates PIK3CA, PNKP, PLK1 NTRK1 755/4885FLT3 159/4885JAK2 510/4885

“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.