SCHEMBL416659

SCHEMBL416659

CC1(C)C2CC[C@@]1(CS(=O)(=O)N1CO1)C(=O)C2

nearest known ligand 0.67

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 3/20 0.67
KMT2A Q03164 4/20 0.63
MEN1 O00255 3/20 0.63
KDM4E B2RXH2 1/20 0.59
ALDH1A1 P00352 2/20 0.56
F2 P00734 2/20 0.55
PRSS1 P07477 2/20 0.55
PRSS2 P07478 2/20 0.55
PRSS3 P35030 2/20 0.55
TSHR P16473 1/20 0.53
HSD17B10 Q99714 1/20 0.53
L3MBTL1 Q9Y468 1/20 0.53
CYP1A2 P05177 1/20 0.52
CYP2C19 P33261 1/20 0.52
CXCR3 P49682 1/20 0.52

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
SCHEMBL1603596 1.00 SMN1; SMN2 (0.67) SMN1; SMN2KMT2AMEN1KDM4EALDH1A1
SCHEMBL306514 1.00 SMN1; SMN2 (0.67) SMN1; SMN2KMT2AMEN1KDM4EALDH1A1
SCHEMBL158053 1.00 SMN1; SMN2 (0.67) SMN1; SMN2KMT2AMEN1KDM4EALDH1A1
SCHEMBL29652034 0.83 SMN1; SMN2 (0.48) SMN1; SMN2KMT2AMEN1KDM4EALDH1A1
SCHEMBL362333 0.83 SMN1; SMN2 (0.48) SMN1; SMN2KMT2AMEN1KDM4EALDH1A1
SCHEMBL6337655 0.83 SMN1; SMN2 (0.48) SMN1; SMN2KMT2AMEN1KDM4EALDH1A1
SCHEMBL6335926 0.83 SMN1; SMN2 (0.48) SMN1; SMN2KMT2AMEN1KDM4EALDH1A1
SCHEMBL6842010 0.83 SMN1; SMN2 (0.48) SMN1; SMN2KMT2AMEN1KDM4EALDH1A1
SCHEMBL29040265 0.83 SMN1; SMN2 (0.82) SMN1; SMN2KMT2AMEN1KDM4EL3MBTL1
SCHEMBL11623286 0.83 SMN1; SMN2 (0.82) SMN1; SMN2KMT2AMEN1KDM4EL3MBTL1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250313590-A1 Phosphoramidite morpholino monomers towards synthesis/convergent synthesis of PMO, TMO, their chimera oligos in 5 prime to 3 prime direction INDIAN ASSOCIATION FOR THE CULTIVATION OF SCIENCE (IACS) (IN) 2025-10-09 US claimed
US-20250001384-A1 APPARATUS AND METHODS FOR SYNTHESIZING BIOPOLYMERS ARIZONA BOARD OF REGENTS ON BEHALF OF ARIZONA STATE UNIVERSITY 2025-01-02 US claimed
US-11912734-B2 Solid-phase synthesis of oligonucleotides containing N6-(2-deoxy-alpha,beta-derythropentofuranosyl)-2,6-diamino-4-hydroxy-5-formamidopyrimidine (Fapy⋅dG) THE JOHNS HOPKINS UNIVERSITY (US) 2024-02-27 US claimed
US-20210291137-A1 APPARATUS AND METHODS FOR SYNTEHSIZING BIOPOLYMERS ARIZONA BOARD OF REGENTS ON BEHALF OF ARIZONA STATE UNIVERSITY (US) 2021-09-23 US claimed
US-20210238213-A1 SOLID-PHASE SYNTHESIS OF OLIGONUCLEOTIDES CONTAINING N6-(2-DEOXY-ALPHA,BETA-DERYTHROPENTOFURANOSYL)-2,6-DIAMINO-4-HYDROXY-5-FORMAMIDOPYRIMIDINE (Fapy.dG) THE JOHNS HOPKINS UNIVERSITY 2021-08-05 US claimed
EP-2711370-B1 METHOD FOR PRODUCING OLIGONUCLEOTIDES AJINOMOTO KK (JP) 2018-01-03 EP claimed
EP-2459525-B1 ENANTIO- AND STEREO-SPECIFIC SYNTHESES OF -AMINO- - HYDROXY AMIDES MERCK SHARP & DOHME (US) 2017-03-01 EP claimed
US-9029528-B2 Solution-based method of making oligonucleotides via phosphoramidite coupling AJINOMOTO CO., INC. (JP) 2015-05-12 US claimed
EP-2711370-A1 METHOD FOR PRODUCING OLIGONUCLEOTIDE Ajinomoto Co., Inc. (JP) 2014-03-26 EP claimed
US-20120296074-A1 PRODUCTION METHOD OF OLIGONUCLEOTIDE AJINOMOTO CO., INC. (JP) 2012-11-22 US claimed
US-20040215016-A1 Stereospecific enrichment of heterocyclic enantiomers R.T. ALAMO VENTURES I, LLC 2004-10-28 US claimed
US-6809195-B1 COMPRISES A MODIFIED PHOSPHORAMIDITE PROTOCOL IN WHICH OXIDATION AND CAPPING STEPS ARE COMBINED INTO A SINGLE STEP; INCREASED EFFICIENCY; SOLID PHASE SYNTHESIS ISIS PHARMACEUTICALS, INC. 2004-10-26 US claimed
US-20040198972-A1 Processes for the preparation of oligonucleotides ISIS PHARMACEUTICALS, INC. 2004-10-07 US claimed
US-20040192912-A1 Process for preparing the antiviral agent [1S-(1alpha,3 alpha,4beta)]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one BRISTOL-MYERS SQUIBB COMPANY 2004-09-30 US claimed
US-6730790-B2 INCLUDING RACEMIC MONOCHLOROFLOSEQUINAN, PURIFIED ENANTIOMERS OF MONOCHLOROFLOSEQUINAN AND SULFONE DERIVATIVE OF MONOCHLOROFLOSEQUINAN R.T. ALAMO VENTURES I. LLC 2004-05-04 US claimed
US-6649764-B2 Racemization of flusequinan using triphenylphosphine and 10-camphorsulfonyl-oxaziridine to form racemic mixtures R. T. ALAMO VENTURES I, LLC 2003-11-18 US claimed
US-6639061-B1 Rodified oligonucleotides that bear 3'-methylene phosphonate or phosphodiester linkages between constituent monomer nucleoside units ISIS PHARMACEUTICALS, INC. 2003-10-28 US claimed
US-20030166677-A1 CHLORINATED HETEROCYCLIC COMPOUNDS AND METHODS OF SYNTHESIS R.T. ALAMO VENTURES I, LLC 2003-09-04 US claimed
US-20030139586-A1 C3' -methylene hydrogen phosphonate oligomers and related compounds COOK PHILLIP DAN (US) 2003-07-24 US claimed
US-20030120075-A1 Stereospecific enrichment of heterocyclic enantiomers R.T. ALAMO ADVENTURES I, LLC 2003-06-26 US 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 (10 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-20250313590-A1 Phosphoramidite morpholino monomers towards synthesis/convergent synthesis of PMO, TMO, their chimera oligos in 5 prime to 3 prime direction MTAP, METTL14, M6PR SMN1; SMN2 1256/4885KMT2A 3591/4885MEN1 1315/4885
US-20030139586-A1 C3' -methylene hydrogen phosphonate oligomers and related compounds NT5C3B, NUDT1, MTAP SMN1; SMN2 2377/4885KMT2A 3080/4885MEN1 659/4885
US-20040192912-A1 Process for preparing the antiviral agent [1S-(1alpha,3 alpha,4beta)]-2-amino-1,9-dihydro-9-[4-hydroxy-3-(hydroxymethyl)-2-methylenecyclopentyl]-6H-purin-6-one SAMHD1, NUDT1, ENTPD1 SMN1; SMN2 2454/4885KMT2A 2959/4885MEN1 3108/4885
US-20030166677-A1 CHLORINATED HETEROCYCLIC COMPOUNDS AND METHODS OF SYNTHESIS STS, SCLY, HCCS SMN1; SMN2 4873/4885KMT2A 1092/4885MEN1 1262/4885
US-20040198972-A1 Processes for the preparation of oligonucleotides RNGTT, RNMT, NUDT1 SMN1; SMN2 1547/4885KMT2A 3566/4885MEN1 3129/4885
US-20210238213-A1 SOLID-PHASE SYNTHESIS OF OLIGONUCLEOTIDES CONTAINING N6-(2-DEOXY-ALPHA,BETA-DERYTHROPENTOFURANOSYL)-2,6-DIAMINO-4-HYDROXY-5-FORMAMIDOPYRIMIDINE (Fapy.dG) DPYD, TYMP, RNGTT SMN1; SMN2 769/4885KMT2A 1684/4885MEN1 3043/4885
US-20120296074-A1 PRODUCTION METHOD OF OLIGONUCLEOTIDE RNGTT, POLM, RNMT SMN1; SMN2 938/4885KMT2A 3808/4885MEN1 2987/4885
US-20040215016-A1 Stereospecific enrichment of heterocyclic enantiomers CBR3, POR, CBR1 SMN1; SMN2 3953/4885KMT2A 3103/4885MEN1 3536/4885
US-20030120075-A1 Stereospecific enrichment of heterocyclic enantiomers CBR3, POR, CBR1 SMN1; SMN2 3953/4885KMT2A 3103/4885MEN1 3536/4885
US-11912734-B2 Solid-phase synthesis of oligonucleotides containing N6-(2-deoxy-alpha,beta-derythropentofuranosyl)-2,6-diamino-4-hydroxy-5-formamidopyrimidine (Fapy⋅dG) DPYD, TYMP, RNGTT SMN1; SMN2 722/4885KMT2A 1513/4885MEN1 3096/4885

“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.