SCHEMBL355917

SCHEMBL355917

O=c1[nH]cnc2c1N=C[N]2

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
ALDH1A1 P00352 2/20 0.40
PARP1 P09874 9/20 0.38
PDPK1 O15530 4/20 0.38
SMN1; SMN2 Q16637 3/20 0.38
CA12 O43570 1/20 0.38
ALOX15 P16050 1/20 0.38
CA9 Q16790 1/20 0.38
TNKS2 Q9H2K2 1/20 0.38
AURKA O14965 1/20 0.34
DAPK3 O43293 1/20 0.34
JAK2 O60674 1/20 0.34
PRKD3 O94806 1/20 0.34
MAP4K4 O95819 1/20 0.34
PAK4 O96013 1/20 0.34
ABL1 P00519 1/20 0.34
CSF1R P07333 1/20 0.34
RET P07949 1/20 0.34
IGF1R P08069 1/20 0.34
MET P08581 1/20 0.34
PDGFRB P09619 1/20 0.34

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
SCHEMBL1867923 0.83 ALDH1A1 (0.40) ALDH1A1PARP1PDPK1SMN1; SMN2CA12
SCHEMBL24783219 0.69 ALDH1A1 (0.35) ALDH1A1PARP1PDPK1SMN1; SMN2CA12
SCHEMBL3245216 0.65 ALDH1A1 (0.39) ALDH1A1PARP1PDPK1SMN1; SMN2CA12
SCHEMBL29561093 0.65 ALDH1A1 (0.39) ALDH1A1PARP1PDPK1SMN1; SMN2CA12
SCHEMBL142922 0.64 QTRT1 (0.42) DYRK1AXDHPNP
SCHEMBL14793587 0.64 ALDH1A1 (0.38) ALDH1A1PARP1PDPK1SMN1; SMN2CA12
SCHEMBL14793621 0.64 HPGD (0.38) ALDH1A1PARP1PDPK1SMN1; SMN2CA12
SCHEMBL4455591 0.64
SCHEMBL2790086 0.62 TDP1 (0.31) LMNA
SCHEMBL5110684 0.62 MAPT (0.38) PARP1AURKAGSK3B

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-112105627-B Unnatural base pair compositions and methods of use 斯克利普斯研究所 2024-07-02 CN claimed
US-11814407-B2 Multiple coupling and oxidation method ROCHE INNOVATION CENTER COPENHAGEN A/S (CH) 2023-11-14 US claimed
US-20230257413-A1 ARTIFICIAL NUCLEIC ACID, METHOD FOR PRODUCING SAME, AND USE THEREOF RIKEN GENESIS CO., LTD. (JP) 2023-08-17 US claimed
EP-4219517-A1 NOVEL ARTIFICIAL NUCLEIC ACID, METHOD FOR PRODUCING SAME, AND USE THEREOF Riken Genesis Co., Ltd. (JP) 2023-08-02 EP claimed
CN-116322706-A Novel artificial nucleic acid, method for producing same, and use thereof 株式会社理真思 2023-06-23 CN claimed
CN-115677810-A Double-stranded oligonucleotide, composition containing double-stranded oligonucleotide, conjugate, preparation method and application 苏州瑞博生物技术股份有限公司 2023-02-03 CN claimed
CN-113646007-A Novel artificial nucleic acid, method for producing same, and use thereof 希森美康株式会社 2021-11-12 CN claimed
US-11142545-B2 Synthesis of thiolated oligonucleotides without a capping step BIOGEN MA INC. (US) 2021-10-12 US claimed
US-11001602-B2 Diarylsulfide backbone containing photolabile protecting groups ROCHE DIAGNOSTICS OPERATIONS, INC. (US) 2021-05-11 US claimed
US-10947262-B2 Hydrophobic interaction chromatography for purification of oligonucleotides BIOGEN MA INC. (US) 2021-03-16 US claimed
US-4999428-A Process for preparing cyclopentyl purine derivatives SCHERING CORPORATION (US) 1991-03-12 US claimed
EP-0412995-A1 CYCLOPENTYL PURINE DERIVATIVES, INTERMEDIATES AND PROCESSES FOR PREPARATION SCHERING CORPORATION (US) 1991-02-20 EP claimed
EP-0253412-B1 N-PHOSPHONYLMETHOXYALKYL DERIVATIVES OF PYRIMIDINE AND PURINE BASES, METHODS FOR THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS THEREFROM WITH ANTIVIRAL ACTIVITY Ceskoslovenska akademie ved (CS) 1990-10-31 EP claimed
EP-0339842-A2 Novel oligoribonucleotide derivatives and application thereof to antiviral agents ISIS PHARMACEUTICALS, INC. (US) 1989-11-02 EP claimed
WO-1989010367-A1 CYCLOPENTYL PURINE DERIVATIVES, INTERMEDIATES AND PROCESSES FOR PREPARATION SCHERING CORPORATION (US) 1989-11-02 WO claimed
EP-0338842-A1 Cyclopentyl purine derivatives, intermediates and processes for preparation SCHERING CORPORATION (US) 1989-10-25 EP claimed
EP-0278501-A2 Nucleotide analogs, their production and use Takeda Chemical Industries, Ltd. (JP) 1988-08-17 EP claimed
EP-0253412-A2 N-Phosphonylmethoxyalkyl derivatives of pyrimidine and purine bases, methods for their preparation and pharmaceutical compositions therefrom with antiviral activity Ceskoslovenska akademie ved (CS) 1988-01-20 EP claimed
EP-0236935-A2 Carboxylic purine nucleosides, their production and use Takeda Chemical Industries, Ltd. (JP) 1987-09-16 EP claimed
EP-0219838-A2 Carbocyclic purine nucleosides, their production and use Takeda Chemical Industries, Ltd. (JP) 1987-04-29 EP 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 (5 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-20230257413-A1 ARTIFICIAL NUCLEIC ACID, METHOD FOR PRODUCING SAME, AND USE THEREOF NSUN2, NSUN3, POLRMT ALDH1A1 986/4885PARP1 556/4885PDPK1 4329/4885
US-11001602-B2 Diarylsulfide backbone containing photolabile protecting groups CRY2, PRXL2A, MGMT ALDH1A1 1217/4885PARP1 2517/4885PDPK1 3811/4885
US-11814407-B2 Multiple coupling and oxidation method RNGTT, PCNA, TYMP ALDH1A1 932/4885PARP1 361/4885PDPK1 2115/4885
US-10947262-B2 Hydrophobic interaction chromatography for purification of oligonucleotides IPO5, IPO4, PHAX ALDH1A1 4330/4885PARP1 1981/4885PDPK1 4820/4885
US-11142545-B2 Synthesis of thiolated oligonucleotides without a capping step RNGTT, NSUN3, NSUN2 ALDH1A1 2661/4885PARP1 1750/4885PDPK1 4355/4885

“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.