SCHEMBL3893181

SCHEMBL3893181

CN(C)C(n1nnc2ccccc21)=[N+](C)C

nearest known ligand 0.57

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ DGAT1 O75907 1/20 0.57
▸ KMT2A Q03164 3/20 0.51
▸ MAPT P10636 2/20 0.51
▸ KDM4E B2RXH2 1/20 0.51
▸ ALDH1A1 P00352 1/20 0.51
▸ HTT P42858 1/20 0.51
▸ NPSR1 Q6W5P4 1/20 0.51
▸ GAA P10253 11/20 0.47
▸ MGAM O43451 10/20 0.47
▸ AMY1A P0DUB6 10/20 0.47
▸ SI P14410 10/20 0.47
▸ MGAM2 Q2M2H8 10/20 0.47
▸ SLC9A1 P19634 2/20 0.47
▸ F2 P00734 2/20 0.47
▸ HPGD P15428 1/20 0.47
▸ POLB P06746 1/20 0.44
▸ MAPK1 P28482 1/20 0.44
▸ ATM Q13315 1/20 0.44
▸ KEAP1 Q14145 1/20 0.44
▸ KCNMA1 Q12791 1/20 0.44

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
SCHEMBL21073734 0.94 DGAT1 (0.51) DGAT1KMT2AMAPTKDM4EALDH1A1
SCHEMBL21904738 0.94 DGAT1 (0.51) DGAT1KMT2AMAPTKDM4EALDH1A1
SCHEMBL1971917 0.94 DGAT1 (0.51) DGAT1KMT2AMAPTKDM4EALDH1A1
SCHEMBL21904737 0.92 DGAT1 (0.49) DGAT1KMT2AMAPTKDM4EALDH1A1
SCHEMBL2732055 0.83 DGAT1 (0.49) DGAT1KMT2AMAPTKDM4EALDH1A1
SCHEMBL29031460 0.83 DGAT1 (0.49) DGAT1KMT2AMAPTKDM4EALDH1A1
SCHEMBL29354525 0.77 TUBB4A (0.44) DGAT1KMT2AMAPTKDM4EALDH1A1
SCHEMBL12019911 0.77 TUBB4A (0.44) DGAT1KMT2AMAPTKDM4EALDH1A1
SCHEMBL1277493 0.77 TUBB4A (0.44) DGAT1KMT2AMAPTKDM4EALDH1A1
SCHEMBL425007 0.77 KMT2A (0.61) DGAT1KMT2AMAPTKDM4EALDH1A1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
WO-2023141692-A1 SYNTHETIC GLYCOLIPIDS AND GLYCOLIPOSOME COMPOSITIONS SUITABLE FOR CARGO DELIVERY TO THE CENTRAL NERVOUS SYSTEM KORANEX CAPITAL (CA) 2023-08-03 — — WO claimed
US-11708341-B2 Synthesis of (S)-2-amino-4-methyl-((R)-2-methyloxirane-2-yl)-pentan-1-one and pharmaceutically acceptable salts thereof AMGEN INC. 2023-07-25 — — US claimed
EP-3494108-B1 SYNTHESIS OF (S)-2-AMINO-4-METHYL-1-((R)-2-METHYLOXIRANE-2-YL)-PENTAN-1-ONE AND PHARMACEUTICALLY ACCEPTABLE SALTS THEREOF AMGEN INC (US) 2020-10-28 — — EP claimed
CN-114599375-B Nucleic acid delivery promoters 国立大学法人高知大学 2025-02-11 — — CN disclosed
EP-3899532-B1 A LABELLING METHOD TO DISTINGUISH ISOBARIC AMINO ACIDS AND AMINO ACID COMBINATIONS RAPID NOVOR INC (CA) 2024-02-14 — — EP disclosed
WO-2023141692-A1 SYNTHETIC GLYCOLIPIDS AND GLYCOLIPOSOME COMPOSITIONS SUITABLE FOR CARGO DELIVERY TO THE CENTRAL NERVOUS SYSTEM KORANEX CAPITAL (CA) 2023-08-03 — — WO disclosed
US-11708341-B2 Synthesis of (S)-2-amino-4-methyl-((R)-2-methyloxirane-2-yl)-pentan-1-one and pharmaceutically acceptable salts thereof AMGEN INC. 2023-07-25 — — US disclosed
EP-3899532-A1 A LABELLING METHOD TO DISTINGUISH ISOBARIC AMINO ACIDS AND AMINO ACID COMBINATIONS Rapid Novor Inc. (CA) 2021-10-27 — — EP disclosed
WO-2020124252-A1 A LABELLING METHOD TO DISTINGUISH ISOBARIC AMINO ACIDS AND AMINO ACID COMBINATIONS RAPID NOVOR INC. (CA) 2020-06-25 — — WO disclosed
EP-3380455-A1 TRYPANOSOMES INHIBITORS H. Hoffnabb-La Roche Ag (CH) 2018-10-03 — — EP disclosed
CN-108368152-A Improvement in Solid phase peptide synthesis CEM有限公司 2018-08-03 — — CN disclosed
WO-2014001820-A1 JAPANESE CEDAR PEPTIDE FOR PREVENTING OR TREATING ALLERGY CIRCASSIA LIMITED (GB) 2014-01-03 — — WO disclosed
WO-2013179044-A2 CLADOSPORIUM PEPTIDES CIRCASSIA LIMITED (GB) 2013-12-05 — — WO disclosed
WO-2013179043-A1 ALTERNARIA PEPTIDES CIRCASSIA LIMITED (GB) 2013-12-05 — — WO disclosed
US-20090182057-A1 DEUTERATED AMINOGLYCIDAL COMPOUNDS AUSPEX PHARMACEUTICALS, INC. (US) 2009-07-16 — — US disclosed
EP-1487484-B1 USE OF MIXTURES OF LIPOPEPTIDES FOR VACCINE PRODUCTION CENTRE NAT RECH SCIENT (FR) 2009-02-11 — — EP disclosed
EP-1801086-A1 Synthesis of carbon acid amides Synthacon GmbH (DE) 2007-06-27 — — EP disclosed
EP-1315739-B1 METHOD FOR BINDING, IN SOLUTION, A PEPTIDE AND A LIPOPHILIC VECTOR AND USES THEREOF PASTEUR INSTITUT (FR) 2004-08-18 — — EP disclosed
EP-1315739-A2 METHOD FOR BINDING, IN SOLUTION, A PEPTIDE AND A LIPOPHILIC VECTOR AND USES THEREOF INSTITUT PASTEUR DE LILLE Etablissement Public (FR) 2003-06-04 — — EP disclosed
WO-2002020558-A2 METHOD FOR BINDING, IN SOLUTION, A PEPTIDE AND A LIPOPHILIC VECTOR AND USES THEREOF INSTITUT PASTEUR DE LILLE (FR) 2002-03-14 — — 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-20090182057-A1 DEUTERATED AMINOGLYCIDAL COMPOUNDS ADRB2, GLRB, ADRB1 DGAT1 2172/4885KMT2A 3732/4885MAPT 3578/4885
US-11708341-B2 Synthesis of (S)-2-amino-4-methyl-((R)-2-methyloxirane-2-yl)-pentan-1-one and pharmaceutically acceptable salts thereof EPOR, KDM5A, PSMA5 DGAT1 4706/4885KMT2A 98/4885MAPT 4106/4885

“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.

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