SCHEMBL82460

SCHEMBL82460

N[C@](O)(Cc1ccccc1)c1ccccc1

nearest known ligand 0.61

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
CYP1A2 P05177 3/20 0.61
CYP2C9 P11712 3/20 0.61
CYP2C19 P33261 3/20 0.61
SLC6A2 P23975 1/20 0.52
TAAR1 Q96RJ0 1/20 0.52
HIF1A Q16665 2/20 0.52
SMN1; SMN2 Q16637 1/20 0.52
KCNA5 P22460 1/20 0.47
MAPK1 P28482 2/20 0.46
KDM4E B2RXH2 1/20 0.46
LMNA P02545 1/20 0.46
FDPS P14324 1/20 0.45
KIF11 P52732 5/20 0.44
KCNN4 O15554 1/20 0.44
CYP3A4 P08684 2/20 0.43
RECQL P46063 1/20 0.42
CYP2D6 P10635 1/20 0.40

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
SCHEMBL2067595 1.00 CYP1A2 (0.61) CYP1A2CYP2C9CYP2C19SLC6A2TAAR1
SCHEMBL2067126 1.00 CYP1A2 (0.61) CYP1A2CYP2C9CYP2C19SLC6A2TAAR1
SCHEMBL8375787 0.78 CYP1A2 (0.47) CYP1A2CYP2C9CYP2C19TAAR1HIF1A
SCHEMBL2573964 0.78 TAAR1 (0.58) CYP1A2CYP2C9CYP2C19SLC6A2TAAR1
SCHEMBL135743 0.78 TAAR1 (0.58) CYP1A2CYP2C9CYP2C19SLC6A2TAAR1
SCHEMBL8098084 0.78 TAAR1 (0.58) CYP1A2CYP2C9CYP2C19SLC6A2TAAR1
SCHEMBL2406230 0.76 SLC6A2 (0.56) CYP1A2CYP2C9CYP2C19SLC6A2TAAR1
Hydrochloric Acid SCHEMBL11784213 0.76 SLC6A2 (0.56) CYP1A2CYP2C9CYP2C19SLC6A2TAAR1
SCHEMBL2790358 0.76 TAAR1 (0.50) CYP1A2CYP2C9CYP2C19TAAR1HIF1A
SCHEMBL912792 0.76 CYP2C9 (0.67) CYP1A2CYP2C9CYP2C19SLC6A2TAAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
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
US-7902207-B2 Process for production of amines TAKASAGO INTERNATIONAL CORPORATION (JP) 2011-03-08 US disclosed
US-20090318421-A1 Polycyclic carbamoylpyridone derivative having hiv integrase inhibitory activity VIIV HEALTHCARE COMPANY 2009-12-24 US disclosed
US-7531657-B2 Method for preparing sulphostin and analogue thereof or preparation intermediate thereof NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2009-05-12 US disclosed
US-20070142639-A1 Process for production of amines TAKASAGO INTERNATIONAL CORPORATION (JP) 2007-06-21 US disclosed
US-20050020834-A1 Method for preparation of sulphostin and its analogue or intermediates thereof NIPPON KAYAKU KABUSHIKI KAISHA (JP) 2005-01-27 US disclosed
EP-1457494-A1 PROCESSES FOR PREPARATION OF SULPHOSTIN AND ITS ANALOGUES OR INTERMEDIATES THEREOF Nippon Kayaku Kabushiki Kaisha (JP) 2004-09-15 EP 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-20050020834-A1 Method for preparation of sulphostin and its analogue or intermediates thereof SOST, PTMS, FGF23 CYP1A2 3890/4885CYP2C9 3495/4885CYP2C19 4034/4885
US-20070142639-A1 Process for production of amines SMS, CCNT1, PEAK1 CYP1A2 287/4885CYP2C9 505/4885CYP2C19 460/4885
US-20090318421-A1 Polycyclic carbamoylpyridone derivative having hiv integrase inhibitory activity NR4A1, NCOA4, NR4A2 CYP1A2 1565/4885CYP2C9 1767/4885CYP2C19 1075/4885

“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.