Fludarabine

Fludarabine

SCHEMBL1981701

Nc1nc(F)nc2c1ncn2C1O[C@H](CO)[C@@H](O)[C@@H]1O

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ LMNA P02545 1/20 1.00
▸ NT5E P21589 1/20 1.00
▸ HIF1A Q16665 1/20 1.00
▸ ADORA2A P29274 7/20 0.73
▸ ADORA2B P29275 5/20 0.73
▸ ADORA3 P0DMS8 3/20 0.71
▸ CA5A P35218 1/20 0.70
▸ ADORA1 P30542 2/20 0.69
▸ DPP4 P27487 1/20 0.69
▸ MEN1 O00255 1/20 0.69
▸ SLC28A1 O00337 1/20 0.69
▸ MAP3K7 O43318 1/20 0.69
▸ SLC28A2 O43868 1/20 0.69
▸ GAPDH P04406 1/20 0.69
▸ MAPK1 P28482 1/20 0.69
▸ STAT6 P42226 1/20 0.69
▸ PI4KA P42356 1/20 0.69
▸ KMT2A Q03164 1/20 0.69
▸ SMN1; SMN2 Q16637 1/20 0.69
▸ PI4K2B Q8TCG2 1/20 0.69

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
Fludarabine SCHEMBL14031844 1.00 LMNA (1.00) LMNANT5EHIF1AADORA2AADORA2B
Fludarabine SCHEMBL5505924 1.00 LMNA (1.00) LMNANT5EHIF1AADORA2AADORA2B
Fludarabine SCHEMBL12232219 1.00 LMNA (1.00) LMNANT5EHIF1AADORA2AADORA2B
Fludarabine SCHEMBL977919 1.00 LMNA (1.00) LMNANT5EHIF1AADORA2AADORA2B
Fludarabine SCHEMBL12018226 1.00 LMNA (1.00) LMNANT5EHIF1AADORA2AADORA2B
Fludarabine SCHEMBL12019517 1.00 LMNA (1.00) LMNANT5EHIF1AADORA2AADORA2B
Fludarabine SCHEMBL3047091 1.00 LMNA (1.00) LMNANT5EHIF1AADORA2AADORA2B
Fludarabine SCHEMBL3655059 1.00 LMNA (1.00) LMNANT5EHIF1AADORA2AADORA2B
Fludarabine SCHEMBL6882489 1.00 LMNA (1.00) LMNANT5EHIF1AADORA2AADORA2B
Fludarabine SCHEMBL13046076 1.00 LMNA (1.00) LMNANT5EHIF1AADORA2AADORA2B

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-20040059104-A1 Nucleotide mimics and their prodrugs BIOTA SCIENTIFIC MANAGEMENT PTY LTD (AU) 2004-03-25 — — US claimed
EP-2509990-A1 NOVEL PHOSPH(ON)ATE- AND SULF(ON)ATE-BASED PHOSPHATE MODIFIED NUCLEOSIDES USEFUL AS SUBSTRATES FOR POLYMERASES AND AS ANTIVIRAL AGENTS Katholieke Universiteit Leuven, K.U. Leuven R&D (BE) 2012-10-17 — — EP disclosed
US-20120245029-A1 NOVEL PHOSPH(ON)ATE- AND SULF(ON)ATE-BASED PHOSPHATE MODIFIED NUCLEOSIDES USEFUL AS SUBSTRATES FOR POLYMERASES AND AS ANTIVIRAL AGENTS KATHOLIEKE UNIVERSITEIT LEUVEN (BE) 2012-09-27 — — US disclosed
WO-2011069688-A1 NOVEL PHOSPH(ON)ATE- AND SULF(ON)ATE-BASED PHOSPHATE MODIFIED NUCLEOSIDES USEFUL AS SUBSTRATES FOR POLYMERASES AND AS ANTIVIRAL AGENTS KATHOLIEKE UNIVERSITEIT LEUVEN, K.U. LEUVEN R&D (BE) 2011-06-16 — — WO disclosed
US-7678782-B2 Bile-acid derived compounds for enhancing oral absorption and systemic bioavailability of drugs XENOPORT, INC. (US) 2010-03-16 — — US disclosed
EP-1974026-A2 MUTANT DEOXYADENOSINE KINASE ENZYMES AND THEIR USE ZGene A/S (DK) 2008-10-01 — — EP disclosed
US-20070248543-A1 Chicken Deoxycytidine and Deoxyadenosine Kinase Enzymes and Their Use ZGENE A/S (DK) 2007-10-25 — — US disclosed
WO-2007079753-A2 MUTANT DEOXYADENOSINE KINASE ENZYMES AND THEIR USE ZGENE A/S (DK) 2007-07-19 — — WO disclosed
EP-1781788-A2 CHICKEN DEOXYCYTIDINE AND DEOXYADENOSINE KINASE ENZYMES AND THEIR USE ZGene A/S (DK) 2007-05-09 — — EP disclosed
US-20070015716-A1 Bile-acid derived compounds for enhancing oral absorption and systemic bioavailability of drugs XENOPORT, INC. 2007-01-18 — — US disclosed
US-6656955-B2 Side effect reduction; synergistic mixture N-GENE RESEARCH LABORATORIES, INC. 2003-12-02 — — US disclosed
EP-1358200-A2 BILE-ACID DERIVED COMPOUNDS FOR ENHANCING ORAL ABSORPTION AND SYSTEMIC BIOAVAILABILITY OF DRUGS Xenoport, Inc. (US) 2003-11-05 — — EP disclosed
US-6440998-B1 Pharmaceutical composition having enhanced antitumor activity and/or reduced side effects, containing an antitumor agent and an hydroximic acid derivative N-GENE RESEARCH LABORATORIES, INC. 2002-08-27 — — US disclosed
US-20020099041-A1 Bile-acid derived compounds for enhancing oral absorption and systemic bioavailability of drugs XENOPORT, INC. 2002-07-25 — — US disclosed
WO-2002044324-A2 BILE-ACID DERIVED COMPOUNDS FOR ENHANCING ORAL ABSORPTION AND SYSTEMIC BIOAVAILABILITY OF DRUGS XENOPORT, INC. (US) 2002-06-06 — — WO disclosed
EP-0993304-A1 PHARMACEUTICAL COMPOSITION HAVING ENHANCED ANTITUMOR ACTIVITY AND/OR REDUCED SIDE EFFECTS, CONTAINING AN ANTITUMOR AGENT AND AN HYDROXAMIC ACID DERIVATIVE N-Gene Research Laboratories Inc. (US) 2000-04-19 — — EP disclosed
WO-1998058676-A1 PHARMACEUTICAL COMPOSITION HAVING ENHANCED ANTITUMOR ACTIVITY AND/OR REDUCED SIDE EFFECTS, CONTAINING AN ANTITUMOR AGENT AND AN HYDROXAMIC ACID DERIVATIVE N-GENE RESEARCH LABORATORIES INC. (US) 1998-12-30 — — WO disclosed
EP-0759926-B1 PROCESS FOR PRODUCING ARABINO-NUCLEOSIDES SCHERING AG (DE) 1998-08-19 — — EP disclosed
US-5712099-A Process for the production of arabinonucleosides SCHERING AKTIENGESELLSCHAFT (DE) 1998-01-27 — — US disclosed
US-4357324-A Prodrug derivatives of 9β-D-arabinofuranosyl-2-fluoroadenine THE UNITED STATES OF AMERICA AS REPRESENTED BY THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 1982-11-02 — — 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 (4 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-20070015716-A1 Bile-acid derived compounds for enhancing oral absorption and systemic bioavailability of drugs SLC10A2, ABCB11, SLC10A1 LMNA 3602/4885NT5E 1333/4885HIF1A 4760/4885
US-20020099041-A1 Bile-acid derived compounds for enhancing oral absorption and systemic bioavailability of drugs SLC10A2, ABCB11, SLC10A1 LMNA 3602/4885NT5E 1333/4885HIF1A 4760/4885
US-20120245029-A1 NOVEL PHOSPH(ON)ATE- AND SULF(ON)ATE-BASED PHOSPHATE MODIFIED NUCLEOSIDES USEFUL AS SUBSTRATES FOR POLYMERASES AND AS ANTIVIRAL AGENTS TYMP, PNP, MTAP LMNA 2238/4885NT5E 224/4885HIF1A 2229/4885
US-20040059104-A1 Nucleotide mimics and their prodrugs NUDT14, ENTPD5, MTAP LMNA 3677/4885NT5E 39/4885HIF1A 1667/4885

“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.

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