SCHEMBL4771047

SCHEMBL4771047

CCN1CCN(c2nc(-c3cc(OC)ccn3)cc3ccccc23)CC1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 3/20 0.51
KMT2A Q03164 3/20 0.51
CYP1A2 P05177 1/20 0.51
CYP2C19 P33261 1/20 0.51
L3MBTL1 Q9Y468 1/20 0.51
DRD2 P14416 1/20 0.47
DRD4 P21917 1/20 0.47
CCR1 P32246 1/20 0.44
CCR5 P51681 1/20 0.44
CCR8 P51685 1/20 0.44
LMNA P02545 1/20 0.44
MAPT P10636 1/20 0.44
TUBB4A P04350 1/20 0.43
TUBB P07437 1/20 0.43
TUBA3C P0DPH7 1/20 0.43
TUBA1B P68363 1/20 0.43
TUBA4A P68366 1/20 0.43
TUBB4B P68371 1/20 0.43
TUBB3 Q13509 1/20 0.43
TUBB2A Q13885 1/20 0.43

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 SCHEMBL6292033 0.99 SMN1; SMN2 (0.50) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
SCHEMBL4763604 0.85 SMN1; SMN2 (0.65) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
SCHEMBL4768407 0.84 TSHR (0.52) SMN1; SMN2KMT2ACYP1A2CYP2C19DRD2
SCHEMBL4763566 0.84 HRH3 (0.48) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
SCHEMBL4774077 0.84 SMN1; SMN2 (0.46) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
Hydrochloric Acid SCHEMBL4763437 0.84 SMN1; SMN2 (0.64) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
Hydrochloric Acid SCHEMBL4764011 0.83 TSHR (0.51) SMN1; SMN2KMT2ACYP1A2CYP2C19DRD2
Hydrochloric Acid SCHEMBL4768944 0.83 SMN1; SMN2 (0.45) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
Hydrochloric Acid SCHEMBL4770729 0.83 HRH3 (0.47) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1
SCHEMBL4774677 0.83 LMNA (0.47) SMN1; SMN2KMT2ACYP1A2CYP2C19L3MBTL1

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 10 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
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 SMN1; SMN2 27/4885KMT2A 1240/4885CYP1A2 2126/4885
US-20040204421-A1 Certain 1,3-disubstituted isoquinoline derivatives MUSK, HTR1A, RYR1 SMN1; SMN2 37/4885KMT2A 1300/4885CYP1A2 1489/4885

“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.