SCHEMBL4764535

SCHEMBL4764535

CCN1CCN(c2nc(-c3nc(C)c(CCO)s3)cc3ccccc23)CC1

nearest known ligand 0.43

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
CYP2D6 P10635 2/20 0.43
CNR1 P21554 1/20 0.43
CNR2 P34972 1/20 0.43
SMN1; SMN2 Q16637 4/20 0.40
KMT2A Q03164 3/20 0.40
CYP1A2 P05177 2/20 0.40
CYP2C19 P33261 2/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
POLB P06746 2/20 0.39
GBA1 P04062 2/20 0.39
HTT P42858 2/20 0.39
HPGD P15428 1/20 0.39
PAX8 Q06710 1/20 0.39
HRH4 Q9H3N8 1/20 0.39
LMNA P02545 1/20 0.39
MAPT P10636 1/20 0.39
NPC1 O15118 1/20 0.38
CYP2C9 P11712 1/20 0.38
RAB9A P51151 1/20 0.38
SRC P12931 1/20 0.38

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
Hydrochloric Acid SCHEMBL4770494 0.99 CYP2D6 (0.42) CYP2D6CNR1CNR2SMN1; SMN2KMT2A
SCHEMBL4763837 0.84 HRH4 (0.41) CYP2D6CNR1CNR2SMN1; SMN2KMT2A
SCHEMBL4772106 0.81 CYP2D6 (0.45) CYP2D6CNR1CNR2SMN1; SMN2KMT2A
Hydrochloric Acid SCHEMBL4768909 0.80 CYP2D6 (0.44) CYP2D6CNR1CNR2SMN1; SMN2KMT2A
SCHEMBL4773924 0.78 SMN1; SMN2 (0.44) CYP2D6CNR1CNR2SMN1; SMN2KMT2A
Hydrochloric Acid SCHEMBL4773289 0.77 SMN1; SMN2 (0.43) CYP2D6CNR1CNR2SMN1; SMN2KMT2A
SCHEMBL4770718 0.76 CYP2D6 (0.47) CYP2D6CNR1CNR2SMN1; SMN2KMT2A
Hydrochloric Acid SCHEMBL4771037 0.75 CYP2D6 (0.46) CYP2D6CNR1CNR2SMN1; SMN2KMT2A
SCHEMBL4773581 0.74 SMN1; SMN2 (0.42) CYP2D6CNR1CNR2SMN1; SMN2KMT2A
SCHEMBL7778369 0.74 KMT2A (0.43) CYP2D6CNR1CNR2SMN1; SMN2KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20020013460-A1 Condensed pyridine compound EISAI CO., LTD 2002-01-31 US claimed
EP-1020445-A1 FUSED PYRIDINE DERIVATIVES Eisai Co., Ltd. (JP) 2000-07-19 EP claimed
EP-1020445-B1 FUSED PYRIDINE DERIVATIVES EISAI R&D MAN CO LTD (JP) 2008-08-13 EP disclosed
US-6875761-B2 Certain 1,3-disubstituted isoquinoline derivatives EISAI CO., LTD. (JP) 2005-04-05 US disclosed
US-20040204421-A1 Certain 1,3-disubstituted isoquinoline derivatives EISAI CO., LTD. 2004-10-14 US disclosed
US-6790844-B2 MUSCLE RELAXANTS; ANTISEROTONINE AGENT EISAI CO., LTD (JP) 2004-09-14 US disclosed
US-20020013460-A1 Condensed pyridine compound EISAI CO., LTD 2002-01-31 US disclosed
US-6340759-B1 ANTISPASMODIC AGENTS EISAI CO., LTD. (JP) 2002-01-22 US disclosed
EP-1020445-A1 FUSED PYRIDINE DERIVATIVES Eisai Co., Ltd. (JP) 2000-07-19 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 (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-20020013460-A1 Condensed pyridine compound MUSK, HTR1A, PAX3 CYP2D6 3573/4885CNR1 475/4885CNR2 220/4885
US-20040204421-A1 Certain 1,3-disubstituted isoquinoline derivatives MUSK, HTR1A, RYR1 CYP2D6 2558/4885CNR1 367/4885CNR2 235/4885

“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.