SCHEMBL3907332

SCHEMBL3907332

c1ccc(CCNC2CCCC2)cc1

nearest known ligand 0.81

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TAAR1 Q96RJ0 2/20 0.81
GRIN2B Q13224 7/20 0.71
SIGMAR1 Q99720 3/20 0.57
GRIN1 Q05586 1/20 0.57
NPC1 O15118 3/20 0.57
RAB9A P51151 3/20 0.57
SMN1; SMN2 Q16637 3/20 0.57
LMNA P02545 1/20 0.57
ALOX12 P18054 1/20 0.57
TP53 P04637 1/20 0.57
EPHX1 P07099 1/20 0.57
TSHR P16473 1/20 0.57
EPHX2 P34913 1/20 0.57
OPRM1 P35372 1/20 0.56
OPRL1 P41146 1/20 0.56
ALDH1A1 P00352 4/20 0.53
MEN1 O00255 1/20 0.53
KMT2A Q03164 1/20 0.53
KDM4E B2RXH2 1/20 0.50
MAPT P10636 1/20 0.50

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
SCHEMBL22216853 0.98 TAAR1 (0.84) TAAR1GRIN2BSIGMAR1GRIN1NPC1
SCHEMBL1240954 0.98 TAAR1 (0.84) TAAR1GRIN2BSIGMAR1GRIN1NPC1
SCHEMBL21792273 0.98 TAAR1 (0.84) TAAR1GRIN2BSIGMAR1GRIN1NPC1
SCHEMBL25002632 0.98 TAAR1 (0.84) TAAR1GRIN2BSIGMAR1GRIN1NPC1
SCHEMBL5332051 0.98 TAAR1 (0.84) TAAR1GRIN2BSIGMAR1GRIN1NPC1
SCHEMBL24075499 0.98 TAAR1 (0.84) TAAR1GRIN2BSIGMAR1GRIN1NPC1
SCHEMBL3665298 0.98 TAAR1 (0.84) TAAR1GRIN2BSIGMAR1GRIN1NPC1
SCHEMBL24767088 0.98 TAAR1 (0.84) TAAR1GRIN2BSIGMAR1GRIN1NPC1
SCHEMBL3760581 0.96 TAAR1 (0.75) TAAR1GRIN2BSIGMAR1GRIN1NPC1
SCHEMBL662411 0.92 GRIN2B (0.76) TAAR1GRIN2BSIGMAR1GRIN1OPRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230053333-A1 PREPARATION METHOD OF CRYSTAL STRUCTURE ANALYSIS SAMPLE FOR STRUCTURAL ANALYSIS USING CRYSTAL SPONGE METHOD KIRIN HOLDINGS KABUSHIKI KAISHA (JP) 2023-02-23 US disclosed
EP-4006024-A1 HETEROCYCLIC AMIDE COMPOUND, PREPARATION METHOD THEREFOR AND USE THEREOF Shanghai Jemincare Pharmaceuticals Co., Ltd. (CN) 2022-06-01 EP disclosed
US-7994326-B2 For treatment of various forms of neurodegeneration, including that from stroke, Alzheimer's disease, Parkinson's disease, and Huntington's disease NORTHWESTERN UNIVERSITY (US) 2011-08-09 US disclosed
EP-2018364-A1 THERAPEUTIC FLUOROETHYL UREAS Allergan, Inc. (US) 2009-01-28 EP disclosed
US-20080108814-A1 Potent and highly selective heteroaromatic inhibitors of neuronal nitric oxide synthase NATIONAL INSTITUTES OF HEALTH (NIH), U.S. DEPT. OF HEALTH AND HUMAN SERVICES (DHHS), U.S. GOVERNMENT 2008-05-08 US disclosed
WO-2007137029-A1 THERAPEUTIC FLUOROETHYL UREAS ALLERGAN, INC. (US) 2007-11-29 WO disclosed
CN-1514831-A Medicinal composition containing 1,3-thiazine derivative ��Ұ����ҩ��ʽ���� 2004-07-21 CN disclosed
CN-1387519-A 2-imino-1, 3-thiazine derivatives SHIONOGI & CO (JP) 2002-12-25 CN 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 (1 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-20080108814-A1 Potent and highly selective heteroaromatic inhibitors of neuronal nitric oxide synthase NOS1, NOS2, NOS3 TAAR1 1066/4885GRIN2B 65/4885SIGMAR1 896/4885

“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.