SCHEMBL2546576

SCHEMBL2546576

CCCCC[C@@]1(n2ccc(=O)[nH]c2=O)O[C@H](CO)[C@@H](O)[C@H]1O

nearest known ligand 0.43

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
SLC28A1 O00337 1/20 0.43
SLC28A2 O43868 1/20 0.43
SLC29A1 Q99808 1/20 0.43
SLC28A3 Q9HAS3 1/20 0.43
P2RY14 Q15391 2/20 0.37
P2RY2 P41231 2/20 0.34
P2RY4 P51582 1/20 0.34
P2RY12 Q9H244 1/20 0.33
P2RY1 P47900 1/20 0.33
P2RY6 Q15077 2/20 0.33

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
SCHEMBL17748428 0.99 SLC28A1 (0.42) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL29508997 0.97 SLC28A1 (0.44) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
Acetic Acid SCHEMBL27645915 0.96 SLC28A1 (0.40) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL5567913 0.93 SLC28A1 (0.38) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL6879975 0.92 SLC28A1 (0.45) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL5616451 0.90 SLC28A1 (0.41) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL29512365 0.89 SLC28A1 (0.43) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL30906577 0.89 SLC28A1 (0.35) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL7456571 0.88 SLC28A1 (0.42) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14
SCHEMBL4064968 0.88 SLC28A1 (0.44) SLC28A1SLC28A2SLC29A1SLC28A3P2RY14

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-110156859-A Mustard seed acid compounds and its preparation method and application 中国科学院新疆理化技术研究所 2019-08-23 CN claimed
WO-2011133580-A1 USE OF DRUGS THAT ACTIVATE P2Y RECEPTORS TO ENHANCE SYNAPTOGENESIS BACK BAY SCIENTIFIC LLC (US) 2011-10-27 WO claimed
US-20110257109-A1 USE OF DRUGS THAT ACTIVATE P2Y RECEPTORS TO ENHANCE SYNAPTOGENESIS BACK BAY SCIENTIFIC, LLC 2011-10-20 US claimed
EP-3445368-B1 COMPOUNDS AND METHODS FOR TREATING NEUROLOGICAL AND CARDIOVASCULAR CONDITIONS ASTROCYTE PHARMACEUTICALS INC (US) 2024-07-17 EP disclosed
US-20240229036-A9 NUCLEIC ACID MEDICINE EXPRESSING SPLICING VARIANT OF MYOSTATIN KNC LABORATORIES CO., LTD. (JP) 2024-07-11 US disclosed
US-20240132893-A1 NUCLEIC ACID MEDICINE EXPRESSING SPLICING VARIANT OF MYOSTATIN KNC LABORATORIES CO., LTD. (JP) 2024-04-25 US disclosed
US-11958878-B2 Therapeutic agent for glycogen storage disease type IA DAIICHI SANKYO COMPANY, LIMITED (JP) 2024-04-16 US disclosed
EP-4299743-A1 NUCLEIC ACID MEDICINE EXPRESSING SPLICING VARIANT OF MYOSTATIN KNC Laboratories Co., Ltd. (JP) 2024-01-03 EP disclosed
US-11839615-B2 Compounds and methods for treating addiction and related disorders ASTROCYTE PHARMACEUTICALS, INC. (US) 2023-12-12 US disclosed
US-20230272403-A1 ANTISENSE OLIGONUCLEOTIDE INDUCING EXON SKIPPING OF ANGIOTENSIN CONVERTING ENZYME 2 GENE KNC LABORATORIES CO., LTD. (JP) 2023-08-31 US disclosed
EP-4201484-A1 ANTISENSE NUCLEIC ACID INDUCING EXON SKIPPING OF ANGIOTENSIN CONVERTING ENZYME 2 GENE KNC Laboratories Co., Ltd. (JP) 2023-06-28 EP disclosed
US-6316426-B1 NUCLEOSIDE DERIVATIVE FOR DIABETES, HEART DISEASE, CEREBROVASCULAR DISORDERS, PARKINSON'S DISEASE, INFANT RESPIRATORY DISTRESS SYNDROME AND FOR ENHANCEMENT OF PHOSPHOLIPID BIOSYNTHESIS PRO-NEURON, INC. 2001-11-13 US disclosed
US-6274563-B1 ADMINISTERING AS ANTIDIABETIC AGENT PRO-NEURON, INC. 2001-08-14 US disclosed
US-6258795-B1 Acylated uridine and cytidine and uses thereof PRO-NEURON, INC. 2001-07-10 US disclosed
US-5583117-A CARDIOVASCULAR, NERVOUS SYSTEM DISORDERS; DIABETES PRO-NEURON, INC. (US) 1996-12-10 US disclosed
US-5470838-A Method of delivering exogenous uridine or cytidine using acylated uridine or cytidine PRO-NEURON, INC. (US) 1995-11-28 US disclosed
EP-0339075-B1 ACYLATED URIDINE AND CYTIDINE AND USES THEREOF PRO-NEURON, INC. (US) 1993-08-18 EP disclosed
EP-0339075-A4 ACYLATED URIDINE AND CYTIDINE AND USES THEREOF. PRO NEURON INC (US) 1990-04-10 EP disclosed
EP-0339075-A1 ACYLATED URIDINE AND CYTIDINE AND USES THEREOF PRO-NEURON, INC. (US) 1989-11-02 EP disclosed
WO-1989003837-A1 ACYLATED URIDINE AND CYTIDINE AND USES THEREOF PRO-NEURON, INC. (US) 1989-05-05 WO 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 (2 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-11839615-B2 Compounds and methods for treating addiction and related disorders ADORA2A, TAAR5, ADORA3 SLC28A1 345/4885SLC28A2 315/4885SLC29A1 273/4885
US-11958878-B2 Therapeutic agent for glycogen storage disease type IA G6PC1, GAA, GBA3 SLC28A1 97/4885SLC28A2 141/4885SLC29A1 623/4885

“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.