Lodenosine

Lodenosine

SCHEMBL97908

Nc1ncnc2c1ncn2[C@@H]1O[C@H](CO)C[C@@H]1F

nearest known ligand 0.61

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Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
EGFR P00533 1/20 0.61
ERBB2 P04626 1/20 0.61
ADORA3 P0DMS8 4/20 0.59
ADORA2B P29275 3/20 0.59
ADORA2A P29274 2/20 0.59
ADORA1 P30542 2/20 0.59
PI4KA P42356 2/20 0.59
PI4K2B Q8TCG2 2/20 0.59
PI4K2A Q9BTU6 2/20 0.59
PI4KB Q9UBF8 2/20 0.59
DPP4 P27487 1/20 0.59
MEN1 O00255 1/20 0.59
SLC28A1 O00337 1/20 0.59
MAP3K7 O43318 1/20 0.59
SLC28A2 O43868 1/20 0.59
GAPDH P04406 1/20 0.59
MAPK1 P28482 1/20 0.59
STAT6 P42226 1/20 0.59
KMT2A Q03164 1/20 0.59
SMN1; SMN2 Q16637 1/20 0.59

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
Lodenosine SCHEMBL3482 1.00 EGFR (0.61) EGFRERBB2ADORA3ADORA2BADORA2A
Lodenosine SCHEMBL16670086 1.00 EGFR (0.61) EGFRERBB2ADORA3ADORA2BADORA2A
Lodenosine SCHEMBL29663669 1.00 EGFR (0.61) EGFRERBB2ADORA3ADORA2BADORA2A
Lodenosine SCHEMBL29831913 1.00 EGFR (0.61) EGFRERBB2ADORA3ADORA2BADORA2A
Lodenosine SCHEMBL8451244 1.00 EGFR (0.61) EGFRERBB2ADORA3ADORA2BADORA2A
Lodenosine SCHEMBL3483 1.00 EGFR (0.61) EGFRERBB2ADORA3ADORA2BADORA2A
Lodenosine SCHEMBL29421139 1.00 EGFR (0.61) EGFRERBB2ADORA3ADORA2BADORA2A
Lodenosine SCHEMBL29329162 1.00 EGFR (0.61) EGFRERBB2ADORA3ADORA2BADORA2A
Lodenosine SCHEMBL30998176 1.00 EGFR (0.61) EGFRERBB2ADORA3ADORA2BADORA2A
Lodenosine SCHEMBL22869478 1.00 EGFR (0.61) EGFRERBB2ADORA3ADORA2BADORA2A

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 3068 patents — a generic fragment claimed broadly, so it's down-weighted as IP noise. Top by claim status then date:

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260144879-A1 ANTI-VIRAL AND HEPATIC-TARGETED DRUGS AI-BIOPHARMA (FR) 2026-05-28 US claimed
US-20260108619-A1 CONJUGATION LINKERS, CELL BINDING MOLECULE-DRUG CONJUGATES CONTAINING THE LINKERS, METHODS OF MAKING AND USES SUCH CONJUGATES WITH THE LINKERS HANGZHOU DAC BIOTECH CO., LTD. (CN) 2026-04-23 US claimed
US-12576124-B2 Formulation of a conjugate of a tubulysin analog to a cell-binding molecule HANGZHOU DAC BIOTECH CO., LTD (CN) 2026-03-17 US claimed
US-20260021101-A1 COMPOSITIONS AND METHODS FOR TREATING, PREVENTING OR REVERSING AGE-ASSOCIATED INFLAMMATION AND DISORDERS BROWN UNIVERSITY (US) 2026-01-22 US claimed
US-20250339551-A1 AN ANTIBODY-DRUG CONJUGATE HAVING TWO OR MORE DIFFERENT FUNCTIONAL SMALL MOLECULES FOR ENHANCED TREATMENT OF REFRACTORY DISEASES HANGZHOU SEEHE BIOTECHNOLOGY CO., LTD (CN) 2025-11-06 US claimed
EP-4642492-A1 AN ANTIBODY-DRUG CONJUGATE HAVING TWO OR MORE FUNCTIONAL SMALL MOLECULE COMPOUNDS FOR ENHANCED TREATMENT OF REFRACTORY DISEASES Hangzhou Seehe Biotechnology Co., Ltd (CN) 2025-11-05 EP claimed
EP-4642484-A1 TARGETED TREATMENT OF PROSTATE CANCERS AND OTHER TUMORS BY AN ANTIBODY-DRUG CONJUGATE Hangzhou Seehe Biotechnology Co., Ltd (CN) 2025-11-05 EP claimed
CN-120145057-A Soft contrast learning fault diagnosis method based on large language model question-answer dialogue 武汉理工大学 2025-06-13 CN claimed
CN-119740406-A Typhoon vortex initialization method and typhoon vortex initialization system 南京信息工程大学 2025-04-01 CN claimed
US-12220464-B2 Specific conjugation linkers, specific immunoconjugates thereof, methods of making and uses such conjugates thereof HANGZHOU DAC BIOTECH CO., LTD. (CN) 2025-02-11 US claimed
WO-1999064048-A9 INHIBITORS OF HIV REVERSE TRANSCRIPTASE ADVANCED MEDICINE INC (US) 2000-07-20 WO claimed
EP-1003541-A1 INHIBITORS OF HIV REVERSE TRANSCRIPTASE Advanced Medicine, Inc. (US) 2000-05-31 EP claimed
WO-1999064048-A1 INHIBITORS OF HIV REVERSE TRANSCRIPTASE ADVANCED MEDICINE, INC. (US) 1999-12-16 WO claimed
US-5565437-A 2',3'-dideoxy-2'-fluoro-purine nucleosides and methods for using same THE UNITED STATES OF AMERICA AS REPRESENTED BY THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 1996-10-15 US claimed
US-5495010-A Acid stable purine dideoxynucleosides THE UNITED STATES OF AMERICA AS REPRESENTED BY THE DEPARTMENT OF HEALTH AND HUMAN SERVICES (US) 1996-02-27 US claimed
EP-0287313-B1 Acid stable dideoxynucleosides active against the cytopathic effects of human immunodeficiency virus US COMMERCE (US) 1995-01-04 EP claimed
EP-0464137-A4 INHIBITION OF HIV USING SYNERGISTIC COMBINATIONS OF NUCLEOSIDE DERIVATIVES 1992-01-15 EP claimed
EP-0464137-A1 INHIBITION OF HIV USING SYNERGISTIC COMBINATIONS OF NUCLEOSIDE DERIVATIVES ONCOGEN LIMITED PARTNERSHIP (US) 1992-01-08 EP claimed
EP-0428109-A2 Deoxyfluoronucleoside process Bristol-Myers Squibb Company (US) 1991-05-22 EP claimed
WO-1990011081-A1 INHIBITION OF HIV USING SYNERGISTIC COMBINATIONS OF NUCLEOSIDE DERIVATIVES ONCOGEN LIMITED PARTNERSHIP (US) 1990-10-04 WO claimed