SCHEMBL82782

SCHEMBL82782

C[C@@H](CCNCc1cccnc1)N(C(=O)O)C(C)(C)C

nearest known ligand 0.52

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
NAMPT P43490 3/20 0.46
CHRM2 P08172 1/20 0.46
CYP1A2 P05177 1/20 0.46
CYP2D6 P10635 1/20 0.46
LMNA P02545 3/20 0.45
L3MBTL1 Q9Y468 1/20 0.45
ALDH1A1 P00352 3/20 0.44
HTT P42858 2/20 0.44
MAPT P10636 1/20 0.44
KMT2A Q03164 2/20 0.43
PKM P14618 1/20 0.43
KDM4E B2RXH2 1/20 0.43
NPSR1 Q6W5P4 1/20 0.42
RECQL P46063 1/20 0.42
HPGD P15428 1/20 0.42
SMN1; SMN2 Q16637 1/20 0.42

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
SCHEMBL8921038 0.86 L3MBTL1 (0.43) L3MBTL1ALDH1A1HTTMAPTKMT2A
SCHEMBL28953789 0.77 L3MBTL1 (0.41) NAMPTCYP1A2CYP2D6LMNAL3MBTL1
SCHEMBL2679135 0.77 LMNA (0.55) CHRM2CYP1A2CYP2D6LMNAL3MBTL1
SCHEMBL23607289 0.74 CYP3A4 (0.53) NAMPTCHRM2CYP1A2CYP2D6LMNA
SCHEMBL23607288 0.74 CYP3A4 (0.53) NAMPTCHRM2CYP1A2CYP2D6LMNA
SCHEMBL3587130 0.74 S1PR1 (0.45) ALDH1A1KMT2A
SCHEMBL18423894 0.73 CYP1A2 (0.61) CHRM2CYP1A2CYP2D6LMNAALDH1A1
SCHEMBL82613 0.73 CYP1A2 (0.61) CHRM2CYP1A2CYP2D6LMNAALDH1A1
SCHEMBL1529369 0.72 KDM4E (0.46) CYP1A2LMNAALDH1A1HTTMAPT
Hydrochloric Acid SCHEMBL29464214 0.72 CYP1A2 (0.59) CHRM2CYP1A2CYP2D6LMNAALDH1A1

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 4 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11267823-B2 Substituted 1,2,3,3a,4,5,7,9,13,13a-decahydropyrido[1′,2′:4,5]pyrazino[1,2-a]pyrrolo[1,2-c]pyrimidines having HIV integrase inhibitory activity SHIONOGI & CO., LTD. (JP) 2022-03-08 US disclosed
US-20200339598-A1 POLYCYCLIC CARBAMOYLPYRIDONE DERIVATIVE HAVING HIV INTEGRASE INHIBITORY ACTIVITY SHIONOGI & CO., LTD. (JP) 2020-10-29 US disclosed
US-20160137666-A1 SUBSTITUTED CYCLOPENTA[4,5]OXAZOLO[3,2-a]PYRIDO[1,2-d]PYRAZINES AS HIV INTEGRASE INHIBITORS SHIONOGI & CO., LTD. (JP) 2016-05-19 US disclosed
US-8129385-B2 Substituted 5-hydroxy-3,4,6,9,9a, 10-hexanhydro-2h-1-oxa04a,8a-diaza-anthracene-6,10-dioness SHIONOGI & CO., LTD. (JP) 2012-03-06 US 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 (3 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-20160137666-A1 SUBSTITUTED CYCLOPENTA[4,5]OXAZOLO[3,2-a]PYRIDO[1,2-d]PYRAZINES AS HIV INTEGRASE INHIBITORS NR4A1, NR4A2, NR4A3 NAMPT 1790/4885CHRM2 3164/4885CYP1A2 516/4885
US-11267823-B2 Substituted 1,2,3,3a,4,5,7,9,13,13a-decahydropyrido[1′,2′:4,5]pyrazino[1,2-a]pyrrolo[1,2-c]pyrimidines having HIV integrase inhibitory activity TYMP, TYMS, POLA1 NAMPT 2622/4885CHRM2 4732/4885CYP1A2 652/4885
US-20200339598-A1 POLYCYCLIC CARBAMOYLPYRIDONE DERIVATIVE HAVING HIV INTEGRASE INHIBITORY ACTIVITY NR4A1, NCOA4, NR4A2 NAMPT 994/4885CHRM2 2301/4885CYP1A2 1502/4885

“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.