Eflornithine

Eflornithine

SCHEMBL4510

Cl.NCCCC(N)(C(=O)O)C(F)F.O

nearest known ligand 0.96

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

ODC1

The experimentally established mechanism targets of Eflornithine. 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
▸ ODC1 known ✓ P11926 2/20 0.92
▸ BLM P54132 3/20 0.96
▸ LMNA P02545 3/20 0.96
▸ KDM4E B2RXH2 1/20 0.96
▸ MAPT P10636 1/20 0.96
▸ RAB9A P51151 1/20 0.96
▸ PMP22 Q01453 1/20 0.96
▸ SMN1; SMN2 Q16637 1/20 0.96
▸ ARG1 P05089 3/20 0.59
▸ ARG2 P78540 2/20 0.39
▸ NPSR1 Q6W5P4 2/20 0.34
▸ THRB P10828 2/20 0.32
▸ KMT2A Q03164 2/20 0.32
▸ GABRR3 A8MPY1 1/20 0.32
▸ GABRP O00591 1/20 0.32
▸ GABRD O14764 1/20 0.32
▸ HDAC3 O15379 1/20 0.32
▸ GABBR2 O75899 1/20 0.32
▸ CYP1A2 P05177 1/20 0.32
▸ GABRA1 P14867 1/20 0.32

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
D-Eflornithine SCHEMBL3238104 1.00 BLM (0.96) BLMLMNAKDM4EMAPTRAB9A
Eflornithine, (S)- SCHEMBL559145 1.00 BLM (0.96) BLMLMNAKDM4EMAPTRAB9A
Eflornithine SCHEMBL4809264 1.00 BLM (0.96) BLMLMNAKDM4EMAPTRAB9A
Eflornithine SCHEMBL5051665 1.00 BLM (0.96) BLMLMNAKDM4EMAPTRAB9A
Eflornithine SCHEMBL1397750 1.00 BLM (0.96) BLMLMNAKDM4EMAPTRAB9A
D-Eflornithine SCHEMBL7208883 0.98 BLM (1.00) BLMLMNAKDM4EMAPTRAB9A
Eflornithine SCHEMBL6779168 0.98 BLM (1.00) BLMLMNAKDM4EMAPTRAB9A
Eflornithine, (S)- SCHEMBL6779172 0.98 BLM (1.00) BLMLMNAKDM4EMAPTRAB9A
Eflornithine SCHEMBL3244711 0.98 ODC1 (0.96) BLMLMNAKDM4EMAPTRAB9A
Eflornithine, (S)- SCHEMBL1322403 0.98 BLM (1.00) BLMLMNAKDM4EMAPTRAB9A

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

Appears in 8577 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260137642-A1 METHODS OF TREATING PATIENTS HAVING TYPE 1 DIABETES WITH EFLORNITHINE CANCER PREVENTION PHARMACEUTICALS, INC. (US) 2026-05-21 — — US claimed
US-20260116861-A1 ISOXAZOLE HYDROXAMIC ACIDS AS HISTONE DEACETYLASE 6 INHIBITORS THE GEORGE WASHINGTON UNIVERSITY, A CONGRESSIONALLY CHARTERED NOT-FOR-PROFIT CORPORATION (US) 2026-04-30 — — US claimed
US-12605349-B2 Methods of treating grade 3 astrocytoma Orbus Therapeutics, Inc. (US) 2026-04-21 — — US claimed
US-20260060950-A1 METHODS OF TREATING GRADE 3 ASTROCYTOMA ORBUS THERAPEUTICS INC (US) 2026-03-05 — — US claimed
US-12522572-B2 Isoxazole hydroxamic acids as histone deacetylase 6 inhibitors THE GEORGE WASHINGTON UNIVERSITY, A CONGRESSIONALLY CHARTERED NOT-FOR-PROFIT CORPORATION (US) 2026-01-13 — — US claimed
EP-4524131-A1 SMALL MOLECULES FOR TREATING CANCER, INHABITING CHEMOKINE ACTIVITY AND/OR INDUCING CELL DEATH AlonBio Ltd. (IL) 2025-03-19 — — EP claimed
WO-2025050100-A1 COMPOSITIONS AND METHODS FOR TREATING HAIR AND SKIN CONDITIONS RELATED TO FOLLICULOPILOSEBACEOUS UNITS OLSEN ELISE A (US) 2025-03-06 — — WO claimed
US-12202803-B2 Small molecules for treating cancer, inhibiting chemokine activity and/or inducing cell death ALONBIO LTD. (IL) 2025-01-21 — — US claimed
WO-2024220593-A1 COMPOSITIONS AND METHODS FOR PREVENTION OF CHEMOTHERAPY- OR RADIATION-RELATED HAIR LOSS OLSEN ELISE A (US) 2024-10-24 — — WO claimed
US-20240343697-A1 ISOXAZOLE HYDROXAMIC ACIDS AS HISTONE DEACETYLASE 6 INHIBITORS THE GEORGE WASHINGTON UNIVERSITY, A CONGRESSIONALLY CHARTERED NOT-FOR-PROFIT CORPORATION (US) 2024-10-17 — — US claimed
US-6764493-B1 Tissue removal using biocompatible materials PEARL TECHNOLOGY HOLDINGS, LLC 2004-07-20 — — US claimed
US-6730809-B2 FORMED VIA CHEMICAL REDUCTION AND HYDROLYSIS WITH MINIMAL USE OF HALOGENATED SOLVENTS; COMPRISES USE OF INTERMEDIATES SUCH AS ETHYL 2-BENZYLIDENEAMINO-2-DIFLUOROMETHYL-4-CYANOBUTANOATE WOMEN FIRST HEALTHCARE, INC. 2004-05-04 — — US claimed
EP-1311266-A2 COMBINATION HIV THERAPY INCLUDING CAMPTOTHECIN SuperGen, Inc. (US) 2003-05-21 — — EP claimed
US-20030083384-A1 Processes for the production of alpha-difluoromethyl ornithine (DFMO) BRISTOL-MYERS SQUIBB COMPANY TO WOMEN FIRST HEALTHCARE, INC. 2003-05-01 — — US claimed
EP-0617968-B1 HIV protease inhibitors in pharmaceutical combinations for the treatment of AIDS MERCK & CO INC (US) 2003-01-08 — — EP claimed
EP-0692963-B1 USE OF TERBINAFINE FOR THE THERAPEUTIC TREATMENT OF PNEUMOCYSTOSIS VSL PHARMA LTD (IE) 2002-06-26 — — EP claimed
WO-2002038125-A2 TISSUE REMOVAL USING BIOCOMPATIBLE MATERIALS PEARL TECHNOLOGY HOLDINGS, LLC (US) 2002-05-16 — — WO claimed
WO-2002000168-A2 COMBINATION HIV THERAPY INCLUDING CAMPTOTHECIN SUPERGEN, INC. (US) 2002-01-03 — — WO claimed
EP-0692963-A1 USE OF TERBINAFINE FOR THE THERAPEUTIC TREATMENT OF PNEUMOCYSTOSIS Mendes S.R.L. (IT) 1996-01-24 — — EP claimed
WO-1994020082-A1 USE OF TERBINAFINE FOR THE THERAPEUTIC TREATMENT OF PNEUMOCYSTOSIS MENDES S.R.L. (IT) 1994-09-15 — — WO claimed
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