Clofarabine

Clofarabine

SCHEMBL1467619

Nc1nc(Cl)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@H]1F

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

POLA1POLA2POLD1POLD2POLD3POLD4POLEPOLE2POLE3PRIM1PRIM2RRM1RRM2RRM2B

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

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
PDE2A O00408 8/20 1.00
ADORA3 P0DMS8 2/20 1.00
PDE4D Q08499 2/20 1.00
PDE3A Q14432 2/20 1.00
ADORA2A P29274 1/20 1.00
ADORA1 P30542 1/20 1.00
ADRA1A P35348 1/20 1.00
NT5E P21589 8/20 0.69
CD99 P14209 2/20 0.69
LMNA P02545 3/20 0.64
HIF1A Q16665 1/20 0.64
TP53 P04637 2/20 0.64
PNP P00491 1/20 0.62
HTT P42858 1/20 0.62
SMN1; SMN2 Q16637 1/20 0.62
RXFP1 Q9HBX9 1/20 0.62

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
Clofarabine SCHEMBL12595105 1.00 PDE2A (1.00) PDE2AADORA3PDE4DPDE3AADORA2A
Clofarabine SCHEMBL17752021 1.00 PDE2A (1.00) PDE2AADORA3PDE4DPDE3AADORA2A
Clofarabine SCHEMBL4570563 1.00 PDE2A (1.00) PDE2AADORA3PDE4DPDE3AADORA2A
Clofarabine SCHEMBL5975001 1.00 PDE2A (1.00) PDE2AADORA3PDE4DPDE3AADORA2A
Clofarabine SCHEMBL12139443 1.00 PDE2A (1.00) PDE2AADORA3PDE4DPDE3AADORA2A
Clofarabine SCHEMBL23620882 1.00 PDE2A (1.00) PDE2AADORA3PDE4DPDE3AADORA2A
Clofarabine SCHEMBL15468200 1.00 PDE2A (1.00) PDE2AADORA3PDE4DPDE3AADORA2A
Clofarabine SCHEMBL9040 1.00 PDE2A (1.00) PDE2AADORA3PDE4DPDE3AADORA2A
Clofarabine SCHEMBL10026375 1.00 PDE2A (1.00) PDE2AADORA3PDE4DPDE3AADORA2A
Clofarabine SCHEMBL18739936 1.00 PDE2A (1.00) PDE2AADORA3PDE4DPDE3AADORA2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3427743-A1 ANTI-HEPATOMA-VIRUS AGENT Kagoshima University (JP) 2019-01-16 EP claimed
US-7470784-B2 Methods for synthesizing 2-chloro-9-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)-9H-purin-6-amine SOUTHERN RESEARCH INSTITUTE (US) 2008-12-30 US claimed
EP-1261350-B1 METHODS FOR SYNTHESIZING 2-CHLORO-9-(2-DEOXY-2-FLUORO-BETA-D-ARABINOFURANOSYL)-9H-PURIN-6-AMINE SOUTHERN RES INST (US) 2006-07-12 EP claimed
US-20050288500-A1 Methods for synthesizing 2-chloro-9-(2-deoxy-2-fluoro-B-D-arabinofuranosyl)-9H-purin-6-amine SOUTHERN RESEARCH INSTITUTE (US) 2005-12-29 US claimed
US-6949640-B2 Method for synthesizing 2-chloro-9-(2-fluoro-β-D-arabinofuranosyl)-9H-purin-6-amine SOUTHERN RESEARCH INSTITUTE (US) 2005-09-27 US claimed
EP-1053012-B1 PHARMACEUTICAL COMPOSITIONS COMPRISING PEG-ASPARAGINASE FOR THE TREATMENT OF HIV INFECTIONS ENZON PHARMACEUTICALS INC (US) 2003-07-23 EP claimed
EP-1261350-A4 METHODS FOR SYNTHESIZING 2-CHLORO-9-(2-DEOXY-2-FLUORO-$g(b)-D-ARABINOFURANOSYL)- i 9H /i -PURIN-6-AMINE SOUTHERN RES INST (US) 2003-04-16 EP claimed
US-20030023078-A1 Method for synthesizing 2-chloro-9-(2-fluoro-beta-d-arabinofuranosyl)-9h-purin-6-amine SOUTHERN RESEARCH INSTITUTE 2003-01-30 US claimed
EP-1261350-A1 METHODS FOR SYNTHESIZING 2-CHLORO-9-(2-DEOXY-2-FLUORO-$g(b)-D-ARABINOFURANOSYL)- i 9H /i -PURIN-6-AMINE Southern Research Institute (US) 2002-12-04 EP claimed
WO-2001010454-A9 PHARMACEUTICAL COMPOSITION COMPRISING PEG-ASPARAGINASE FOR THE TREATMENT OF HIV INFECTION AVENTIS PHARM PROD INC (US) 2002-11-07 WO claimed
EP-1143990-A3 PHARMACEUTICAL COMPOSTIONS COMPRISING PEG-ASPARAGINASE FOR THE TREATMENT OF HIV INFECTIONS Aventis Pharmaceuticals Inc. (US) 2002-03-27 EP claimed
EP-1143990-A2 PHARMACEUTICAL COMPOSTIONS COMPRISING PEG-ASPARAGINASE FOR THE TREATMENT OF HIV INFECTIONS Aventis Pharmaceuticals Inc. (US) 2001-10-17 EP claimed
WO-2001060383-A1 METHODS FOR SYNTHESIZING 2-CHLORO-9-(2-DEOXY-2-FLUORO-β-D-ARABINOFURANOSYL)-9H-PURIN-6-AMINE SOUTHERN RESEARCH INSTITUTE (US) 2001-08-23 WO claimed
WO-2001010454-A2 PHARMACEUTICAL COMPOSITION COMPRISING PEG-ASPARAGINASE FOR THE TREATMENT OF HIV INFECTION AVENTIS PHARMACEUTICALS PRODUCTS INC. (US) 2001-02-15 WO claimed
EP-1053012-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING PEG-ASPARAGINASE FOR THE TREATMENT OF HIV INFECTIONS Aventis Pharmaceuticals Products Inc. (US) 2000-11-22 EP claimed
WO-1999039732-A1 PHARMACEUTICAL COMPOSITIONS COMPRISING PEG-ASPARAGINASE FOR THE TREATMENT OF HIV INFECTIONS AVENTIS PHARMACEUTICALS PRODUCTS INC. (US) 1999-08-12 WO claimed
US-5661136-A 2-halo-2'-fluoro ARA adenosines as antinoplastic agents SOUTHERN RESEARCH INSTITUTE (US) 1997-08-26 US claimed
EP-0314011-A2 Purine derivatives F. HOFFMANN-LA ROCHE AG (CH) 1989-05-03 EP claimed
US-10987372-B2 Anti-hepatoma-virus agent KAGOSHIMA UNIVERSITY (JP) 2021-04-27 US disclosed
EP-0314011-A2 Purine derivatives F. HOFFMANN-LA ROCHE AG (CH) 1989-05-03 EP 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-10987372-B2 Anti-hepatoma-virus agent HAVCR2, HDGF, HDGFL3 PDE2A 4650/4885ADORA3 2205/4885PDE4D 4594/4885

“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.