SCHEMBL1461064

SCHEMBL1461064

COc1cccc2[nH]cc(C[C@H](N)C(=O)O)c12

nearest known ligand 0.70

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 3/20 0.61
KDM4E B2RXH2 3/20 0.61
MAPT P10636 3/20 0.61
LMNA P02545 2/20 0.61
TSHR P16473 2/20 0.61
BLM P54132 2/20 0.61
PMP22 Q01453 2/20 0.61
MEN1 O00255 2/20 0.61
MPO P05164 1/20 0.61
HIF1A Q16665 1/20 0.61
HTR2A P28223 4/20 0.58
MTNR1A P48039 1/20 0.56
MTNR1B P49286 1/20 0.56
HTR6 P50406 1/20 0.52
ALDH1A1 P00352 1/20 0.51
CYP3A4 P08684 1/20 0.51
HTR1A P08908 1/20 0.51
ADORA3 P0DMS8 1/20 0.51
ALOX15 P16050 1/20 0.51
NFKB1 P19838 1/20 0.51

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
SCHEMBL18029216 1.00 KMT2A (0.61) KMT2AKDM4EMAPTLMNATSHR
SCHEMBL1461062 1.00 KMT2A (0.61) KMT2AKDM4EMAPTLMNATSHR
SCHEMBL29809866 1.00 KMT2A (0.61) KMT2AKDM4EMAPTLMNATSHR
SCHEMBL2013303 1.00 KMT2A (0.61) KMT2AKDM4EMAPTLMNATSHR
SCHEMBL2013301 0.89 MTNR1A (0.58) KMT2AKDM4EMAPTLMNATSHR
Hydrochloric Acid SCHEMBL28174730 0.88 MTNR1A (0.57) KMT2AKDM4EMAPTLMNATSHR
Hydrochloric Acid SCHEMBL28174732 0.88 MTNR1A (0.57) KMT2AKDM4EMAPTLMNATSHR
SCHEMBL24328917 0.86 SMN1; SMN2 (0.60) KMT2AKDM4EMAPTLMNATSHR
SCHEMBL28409765 0.86 SMN1; SMN2 (0.60) KMT2AKDM4EMAPTLMNATSHR
SCHEMBL24328893 0.86 MTNR1A (0.57) KMT2AKDM4EMAPTLMNATSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117529489-A Bicyclic peptide ligands specific for NK cells 拜斯科技术开发有限公司 2024-02-06 CN claimed
US-20160331725-A1 USE OF COMPOUNDS THAT ARE ABLE TO INCREASE THE SERUM IGF-1 LEVEL FOR THE PREPARATION OF A THERAPEUTICAL COMPOSITION FOR TREATMENT OF VARIOUS DISEASE STATES ASSOCIATED WITH A REDUCED IGF-1 SERUM LEVEL IN HUMANS AND ANIMALS VEIJLEN N.V. 2016-11-17 US claimed
EP-2513016-B1 IMPROVED METHOD FOR PRODUCING INTERMEDIATES FOR THE PRODUCTION OF MACROCYCLES THAT ARE INHIBITORS OF THE PROTEASOMIC DEGRADATION OF P27, SUCH AS ARGYRIN AND DERIVATIVES THEREOF Helmholtz Zentrum für Infektionsforschung GmbH (DE) 2016-02-17 EP claimed
US-8853249-B2 Method for producing intermediates for the production of macrocycles that are inhibitors of the proteasomic degradation of p27, such as argyrin and derivatives thereof Helmholtz-Zentrum für Infektionsforschungs GmbH (DE) 2014-10-07 US claimed
US-20120295941-A1 Method For Producing Intermediates For The Production Of Macrocycles That Are Inhibitors Of The Proteasomic Degradation of P27, Such As Argyrin And Derivatives Thereof GOTTFRIED WILHELM LEIBNIZ UNIVERSITAT (DE) 2012-11-22 US claimed
EP-2513016-A1 IMPROVED METHOD FOR PRODUCING INTERMEDIATES FOR THE PRODUCTION OF MACROCYCLES THAT ARE INHIBITORS OF THE PROTEASOMIC DEGRADATION OF P27, SUCH AS ARGYRIN AND DERIVATIVES THEREOF Helmholtz-Zentrum für Infektionsforschung GmbH (DE) 2012-10-24 EP claimed
EP-2303916-B1 METHOD FOR PRODUCING INTERMEDIATES FOR THE PRODUCTION OF NOVEL MACROCYCLES THAT ARE INHIBITORS OF THE PROTEASOMIC DEGRADATION OF P27, SUCH AS ARGYRIN AND DERIVATIVES THEREOF, AND USES OF SAID MACROCYCLES HELMHOLTZ INFEKTIONSFORSCHUNG (DE) 2012-05-09 EP claimed
US-20110311564-A1 Method for Producing Intermediates for the Production of Novel Macrocycles that are Inhibitors of the Proteasomic Degradation of p27, such as Argyrin and Derivatives Thereof, and Uses of Said Macrocycles GOTTFRIED WILHELM LEIBNIZ UNIVERSITAT HANNOVER (DE) 2011-12-22 US claimed
WO-2011073173-A1 IMPROVED METHOD FOR PRODUCING INTERMEDIATES FOR THE PRODUCTION OF MACROCYCLES THAT ARE INHIBITORS OF THE PROTEASOMIC DEGRADATION OF P27, SUCH AS ARGYRIN AND DERIVATIVES THEREOF Helmholtz-Zentrum für Infektionsforschung GmbH (DE) 2011-06-23 WO claimed
EP-2303916-A1 METHOD FOR PRODUCING INTERMEDIATES FOR THE PRODUCTION OF NOVEL MACROCYCLES THAT ARE INHIBITORS OF THE PROTEASOMIC DEGRADATION OF P27, SUCH AS ARGYRIN AND DERIVATIVES THEREOF, AND USES OF SAID MACROCYCLES Helmholtz-Zentrum für Infektionsforschung GmbH (DE) 2011-04-06 EP claimed
JP-4641942-B2 2011-03-02 JP claimed
WO-2010006682-A1 METHOD FOR PRODUCING INTERMEDIATES FOR THE PRODUCTION OF NOVEL MACROCYCLES THAT ARE INHIBITORS OF THE PROTEASOMIC DEGRADATION OF P27, SUCH AS ARGYRIN AND DERIVATIVES THEREOF, AND USES OF SAID MACROCYCLES Helmholtz-Zentrum für Infektionsforschung GmbH (DE) 2010-01-21 WO claimed
EP-2138507-A1 Method for producing intermediates for the production of novel macrocycles that are inhibitors of the proteasomic degradation of p27, such as argyrin and derivatives thereof, and uses of said macrocycles Helmholtz-Zentrum für Infektionsforschung GmbH (DE) 2009-12-30 EP claimed
US-20080194553-A1 compounds that are capable of increasing the serum level of insulin-like growth factor 1 (IGF-1) for the preparation of a therapeutical composition,in the form of a food supplement, for the treatment of subjects suffering from serious fatigue and exhausting symptoms, burn-out and chronic fatigue syndrome VEIJLEN N.V. (NL) 2008-08-14 US claimed
EP-1670444-A2 USE OF INDOLEACETIC ACID DERIVATIVES WHICH INCREASE THE SERUM IGF-1 LEVEL FOR THE PREPARATION OF A THERAPEUTICAL COMPOSITION FOR TREATMENT OF VARIOUS DISEASES Veijlen N.V. (AN) 2006-06-21 EP claimed
WO-2005039546-A2 USE OF INDOLEACETIC ACID DERIVATIVES WHICH INCREASE THE SERUM IGF-1 LEVEL FOR THE PREPARATION OF A THERAPEUTICAL COMPOSITION FOR TREATMENT OF VARIOUS DISEASES VEIJLEN N.V. (AN) 2005-05-06 WO claimed
CN-122094701-A TLR3 binding bicyclic peptide ligands 2026-05-26 CN disclosed
EP-3894390-B1 SYNTHESIS OF (S)-6-HYDROXYTRYPTOPHAN AND DERIVATIVES THEREOF HEIDELBERG PHARMA RES GMBH (DE) 2026-05-20 EP disclosed
WO-2005039546-A2 USE OF INDOLEACETIC ACID DERIVATIVES WHICH INCREASE THE SERUM IGF-1 LEVEL FOR THE PREPARATION OF A THERAPEUTICAL COMPOSITION FOR TREATMENT OF VARIOUS DISEASES VEIJLEN N.V. (AN) 2005-05-06 WO disclosed
WO-2005034942-A1 ANIMAL FEED COMPOSITION VEIJLEN N.V. (AN) 2005-04-21 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-20120295941-A1 Method For Producing Intermediates For The Production Of Macrocycles That Are Inhibitors Of The Proteasomic Degradation of P27, Such As Argyrin And Derivatives Thereof SKP2, CDKN1A, MDM2 KMT2A 1847/4885KDM4E 1914/4885MAPT 3445/4885
US-20110311564-A1 Method for Producing Intermediates for the Production of Novel Macrocycles that are Inhibitors of the Proteasomic Degradation of p27, such as Argyrin and Derivatives Thereof, and Uses of Said Macrocycles SKP2, CDKN1A, PSMC1 KMT2A 1824/4885KDM4E 1695/4885MAPT 4040/4885

“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.