Fludarabine

Fludarabine

SCHEMBL158659

Nc1nc(F)nc2c1ncn2[C@@H]1O[C@H](CO)[C@@H](O)[C@@H]1O.O=c1[nH]c(=O)n([C@H]2C[C@H](O)[C@@H](CO)O2)cc1F

nearest known ligand 0.65

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

TYMS

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

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.65
NT5E P21589 2/20 0.65
HIF1A Q16665 1/20 0.65
SMN1; SMN2 Q16637 2/20 0.60
CA5A P35218 1/20 0.53
DNMT1 P26358 3/20 0.52
FPR2 P25090 2/20 0.52
DNMT3B Q9UBC3 2/20 0.52
DTYMK P23919 2/20 0.52
PNP P00491 1/20 0.51
TP53 P04637 1/20 0.51
HTT P42858 1/20 0.51
PDE4D Q08499 1/20 0.51
PDE3A Q14432 1/20 0.51
RXFP1 Q9HBX9 1/20 0.51
ADORA2A P29274 2/20 0.51
ADORA3 P0DMS8 2/20 0.51
ADORA2B P29275 1/20 0.50

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 Phosphate SCHEMBL27849470 0.92 CA5A (0.68) LMNANT5EHIF1ASMN1; SMN2CA5A
Fludarabine Phosphate SCHEMBL28143246 0.92 CA5A (0.67) LMNANT5EHIF1ASMN1; SMN2CA5A
Fludarabine Phosphate SCHEMBL28142252 0.87 CA5A (0.59) LMNANT5EHIF1ASMN1; SMN2CA5A
Fludarabine SCHEMBL1674414 0.86 NT5E (0.62) LMNANT5EHIF1ACA5ADTYMK
Fludarabine SCHEMBL4455725 0.85 LMNA (0.47) LMNANT5EHIF1ASMN1; SMN2CA5A
Fludarabine Phosphate SCHEMBL20899648 0.85 CA5A (0.66) LMNANT5EHIF1ASMN1; SMN2CA5A
5-Fluorouridine SCHEMBL4390962 0.83 LMNA (0.83) LMNANT5ESMN1; SMN2
5-Fluorouridine SCHEMBL4390966 0.83 LMNA (0.83) LMNANT5ESMN1; SMN2
Fludarabine SCHEMBL8934950 0.83 LMNA (0.76) LMNANT5EHIF1ASMN1; SMN2CA5A
Fludarabine SCHEMBL1697072 0.83 LMNA (0.76) LMNANT5EHIF1ASMN1; SMN2CA5A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11890276-B2 Methods of treating pancreatic cancer CHEMOCENTRYX, INC. (US) 2024-02-06 US claimed
WO-2023194441-A1 COMBINATION OF HDAC INHIBITORS AND STATINS FOR USE IN THE TREATMENT OF PANCREATIC CANCER ISTITUTO NAZIONALE TUMORI IRCCS - FONDAZIONE G. PASCALE (IT) 2023-10-12 WO claimed
CN-109053595-B Salts of epidermal growth factor receptor kinase inhibitors 西建卡尔有限责任公司 2022-04-01 CN claimed
US-20210401816-A1 METHODS OF TREATING PANCREATIC CANCER CHEMOCENTRYX, INC. 2021-12-30 US claimed
EP-3297438-B1 CCR2 MODULATORS CHEMOCENTRYX INC (US) 2021-10-20 EP claimed
US-11116756-B2 Methods of treating pancreatic cancer CHEMOCENTRYX, INC. (US) 2021-09-14 US claimed
CN-108135168-B CCR2 modulators 凯莫森特里克斯股份有限公司 2021-07-20 CN claimed
US-20200179359-A1 METHODS OF TREATING PANCREATIC CANCER CHEMOCENTRYX, INC. 2020-06-11 US claimed
US-10583131-B2 Methods of treating pancreatic cancer CHEMOCENTRYX, INC. (US) 2020-03-10 US claimed
US-20190350911-A1 METHODS OF TREATING PANCREATIC CANCER CHEMOCENTRYX, INC. 2019-11-21 US claimed
EP-2155177-A2 MODIFICATION OF BIOLOGICAL TARGETING GROUPS FOR THE TREATMENT OF CANCER Intezyne Technologies Incorporated (US) 2010-02-24 EP claimed
US-7638558-B2 drug loaded micelle of a triblock polymer tert-butylphenylsilylpropene-polyethylene glycol-b-poly(tert-butylaspartic acid-b-polyphenylalanine-copoly( tert-buyltyrosine) has a drug-loaded inner core, a crosslinked outer core, and a hydrophilic shell INTEZYNE TECHNOLOGIES, INC. (US) 2009-12-29 US claimed
EP-1907444-B1 POLYMERIC MICELLES FOR DRUG DELIVERY INTEZYNE TECHNOLOGIES INC (US) 2009-08-19 EP claimed
US-20090110662-A1 MODIFICATION OF BIOLOGICAL TARGETING GROUPS FOR THE TREATMENT OF CANCER INTEZYNE TECHNOLOGIES, INC. (US) 2009-04-30 US claimed
US-20090098200-A1 COMPOSITIONS COMPRISING LIPOPHILIC ACTIVE COMPOUNDS AND METHOD FOR THEIR PREPARATION SOLUBEST LTD. (IL) 2009-04-16 US claimed
WO-2009040818-A1 COMPOSITIONS COMPRISING LIPOPHILIC ACTIVE COMPOUNDS AND METHOD FOR THEIR PREPARATION SOLUBEST LTD (IL) 2009-04-02 WO claimed
WO-2008134761-A2 MODIFICATION OF BIOLOGICAL TARGETING GROUPS FOR THE TREATMENT OF CANCER INTEZYNE TECHNOLOGIES, INC. (US) 2008-11-06 WO claimed
EP-1907444-A2 POLYMERIC MICELLES FOR DRUG DELIVERY Intezyne Technologies Incorporated (US) 2008-04-09 EP claimed
US-20060240092-A1 drug loaded micelle of a triblock polymer tert-butylphenylsilylpropene-polyethylene glycol-b-poly(tert-butylaspartic acid-b-polyphenylalanine-copoly( tert-buyltyrosine) has a drug-loaded inner core, a crosslinked outer core, and a hydrophilic shell INTEZYNE TECHNOLOGIES, INC. 2006-10-26 US claimed
WO-2006107903-A2 POLYMERIC MICELLES FOR DRUG DELIVERY INTEZYNE TECHNOLOGIES, INCORPORATED (US) 2006-10-12 WO claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (8 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-20200179359-A1 METHODS OF TREATING PANCREATIC CANCER RNASE1, KRAS, PNLIP LMNA 4359/4885NT5E 2108/4885HIF1A 1570/4885
US-20190350911-A1 METHODS OF TREATING PANCREATIC CANCER RNASE1, KRAS, PNLIP LMNA 4359/4885NT5E 2108/4885HIF1A 1570/4885
US-11116756-B2 Methods of treating pancreatic cancer RNASE1, KRAS, PNLIP LMNA 4359/4885NT5E 2108/4885HIF1A 1570/4885
US-20210401816-A1 METHODS OF TREATING PANCREATIC CANCER RNASE1, KRAS, PNLIP LMNA 4359/4885NT5E 2108/4885HIF1A 1570/4885
US-20060240092-A1 drug loaded micelle of a triblock polymer tert-butylphenylsilylpropene-polyethylene glycol-b-poly(tert-butylaspartic acid-b-polyphenylalanine-copoly( tert-buyltyrosine) has a drug-loaded inner core, a crosslinked outer core, and a hydrophilic shell ABCB1, TERT, ABCB4 LMNA 1309/4885NT5E 4389/4885HIF1A 3482/4885
US-11890276-B2 Methods of treating pancreatic cancer RNASE1, KRAS, PNLIP LMNA 4359/4885NT5E 2108/4885HIF1A 1570/4885
US-20090110662-A1 MODIFICATION OF BIOLOGICAL TARGETING GROUPS FOR THE TREATMENT OF CANCER CD44, CD47, EPCAM LMNA 3626/4885NT5E 709/4885HIF1A 1250/4885
US-10583131-B2 Methods of treating pancreatic cancer RNASE1, KRAS, PNLIP LMNA 4359/4885NT5E 2108/4885HIF1A 1570/4885

“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.