Acadesine

Acadesine

SCHEMBL8722270

NC(=O)c1ncn([C@@H]2O[C@H](CO)[C@@H](O)[C@H]2O)c1N.O=P(O)(O)O

nearest known ligand 0.91

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

PRKAA1PRKAA2PRKAB1PRKAB2PRKAG1PRKAG2PRKAG3

The experimentally established mechanism targets of Acadesine. 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
KDM4E B2RXH2 2/20 0.91
TP53 P04637 2/20 0.91
TDP1 Q9NUW8 1/20 0.91
MAPT P10636 1/20 0.91
ATIC P31939 2/20 0.74
FBP1 P09467 1/20 0.74
SMN1; SMN2 Q16637 4/20 0.70
ALDH1A1 P00352 3/20 0.70
HTT P42858 2/20 0.70
BLM P54132 2/20 0.70
TSHR P16473 2/20 0.70
GAA P10253 1/20 0.70
LMNA P02545 4/20 0.55
THPO P40225 2/20 0.55
PMP22 Q01453 2/20 0.55
GMNN O75496 1/20 0.55
NFKB1 P19838 1/20 0.55
DNMT1 P26358 1/20 0.55
MTOR P42345 1/20 0.55
RAB9A P51151 1/20 0.55

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
Acadesine SCHEMBL30433377 1.00 KDM4E (0.91) KDM4ETP53TDP1MAPTATIC
Acadesine SCHEMBL5053863 0.95 KDM4E (1.00) KDM4ETP53TDP1MAPTATIC
Acadesine SCHEMBL10017743 0.95 KDM4E (1.00) KDM4ETP53TDP1MAPTATIC
Acadesine SCHEMBL14520658 0.95 KDM4E (1.00) KDM4ETP53TDP1MAPTATIC
Acadesine SCHEMBL7141001 0.95 KDM4E (1.00) KDM4ETP53TDP1MAPTATIC
Acadesine SCHEMBL6113798 0.95 KDM4E (1.00) KDM4ETP53TDP1MAPTATIC
Acadesine SCHEMBL2631614 0.95 KDM4E (1.00) KDM4ETP53TDP1MAPTATIC
Acadesine SCHEMBL2394079 0.95 KDM4E (1.00) KDM4ETP53TDP1MAPTATIC
Acadesine SCHEMBL28745421 0.95 KDM4E (1.00) KDM4ETP53TDP1MAPTATIC
Acadesine SCHEMBL2619704 0.95 KDM4E (1.00) KDM4ETP53TDP1MAPTATIC

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 11 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11834469-B2 AMP-activated protein kinase activating compounds and uses thereof SKYLARK BIOSCIENCE LLC (US) 2023-12-05 US disclosed
US-11779590-B2 AMP-activated protein kinase activating compounds and uses thereof SKYLARK BIOSCIENCE LLC (US) 2023-10-10 US disclosed
US-20220133765-A1 AMP-ACTIVATED PROTEIN KINASE ACTIVATING COMPOUNDS AND USES THEREOF SKYLARK BIOSCIENCE LLC (US) 2022-05-05 US disclosed
US-20210230209-A1 AMP-ACTIVATED PROTEIN KINASE ACTIVATING COMPOUNDS AND USES THEREOF SKYLARK BIOSCIENCE LLC (US) 2021-07-29 US disclosed
EP-3833359-A2 AMP-ACTIVATED PROTEIN KINASE ACTIVATING COMPOUNDS AND USES THEREOF Skylark Bioscience LLC (US) 2021-06-16 EP disclosed
CN-112739352-A Compounds that activate AMP-activated protein kinase and uses thereof 斯凯拉克生物科技有限责任公司 2021-04-30 CN disclosed
US-5827831-A Lipid nucleotide analog prodrugs for oral administration NEXSTAR PHARMACEUTICALS, INC. (US) 1998-10-27 US disclosed
US-5744592-A IMPROVING THE BIOAVAILABILITY AND ABSORPTION OF A DRUG THROUGH THE DIGESTIVE TRACT BY COVALENTLY BONDING THE DRUG AND A 1-O-OR-S-ALKYL-SN-GLYCERO-3-PHOSPHATE NEXSTAR PHARMACEUTICALS, INC. (US) 1998-04-28 US disclosed
US-5506347-A ADENOSINE KINASE INHIBITOR GENSIA, INC. (US) 1996-04-09 US disclosed
US-5484809-A ANTITUMOR VESTAR, INC. (US) 1996-01-16 US disclosed
US-5411947-A converting drugs having suitable functional groups to 1-O-alkyl-, 1-O-acyl-, 1-S-acyl, and 1-S-alkyl-sn-glycero-3-phosphate derivatives; drugs such as AZT, cladribine, AICA-Riboside VESTAR, INC. (US) 1995-05-02 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-20210230209-A1 AMP-ACTIVATED PROTEIN KINASE ACTIVATING COMPOUNDS AND USES THEREOF PRKAG1, PRKAG2, PRKAG3 KDM4E 3446/4885TP53 858/4885TDP1 1958/4885
US-20220133765-A1 AMP-ACTIVATED PROTEIN KINASE ACTIVATING COMPOUNDS AND USES THEREOF MYLK2, PRKAG1, PRKAG3 KDM4E 2380/4885TP53 432/4885TDP1 221/4885
US-11779590-B2 AMP-activated protein kinase activating compounds and uses thereof MYLK2, PRKAG1, PRKAG3 KDM4E 2380/4885TP53 432/4885TDP1 221/4885
US-11834469-B2 AMP-activated protein kinase activating compounds and uses thereof PRKAG1, PRKAG2, PRKAG3 KDM4E 3603/4885TP53 898/4885TDP1 2079/4885

“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.