SCHEMBL4770422

SCHEMBL4770422

CCN1CCN(c2nc(-c3ccccc3OCCO[Si](C)(C)C(C)(C)C)cc3ccccc23)CC1

nearest known ligand 0.41

Predicted protein targets (top 18)

geneUniProtsupporting neighboursconfidence
KMT2A Q03164 5/20 0.40
SMN1; SMN2 Q16637 3/20 0.40
CYP1A2 P05177 1/20 0.40
CYP2C19 P33261 1/20 0.40
L3MBTL1 Q9Y468 1/20 0.40
MEN1 O00255 3/20 0.39
PIK3CD O00329 1/20 0.38
GBA1 P04062 1/20 0.37
POLB P06746 1/20 0.37
HPGD P15428 1/20 0.37
HTT P42858 1/20 0.37
PAX8 Q06710 1/20 0.37
ALDH1A1 P00352 3/20 0.37
KDM4E B2RXH2 2/20 0.37
TDP1 Q9NUW8 1/20 0.37
LMNA P02545 1/20 0.36
MAPT P10636 1/20 0.36
CNR2 P34972 2/20 0.36

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
SCHEMBL4770549 0.85 ROCK2 (0.37) KMT2ASMN1; SMN2CYP1A2CYP2C19L3MBTL1
SCHEMBL4770609 0.84 KMT2A (0.47) KMT2ASMN1; SMN2CYP1A2CYP2C19L3MBTL1
SCHEMBL4770426 0.84 CYP2D6 (0.39) KMT2ASMN1; SMN2CYP1A2CYP2C19L3MBTL1
Hydrochloric Acid SCHEMBL4766222 0.84 KMT2A (0.47) KMT2ASMN1; SMN2CYP1A2CYP2C19L3MBTL1
SCHEMBL4767474 0.83 SMN1; SMN2 (0.38) KMT2ASMN1; SMN2CYP1A2CYP2C19L3MBTL1
SCHEMBL4768653 0.81 CYP1A2 (0.48) KMT2ASMN1; SMN2CYP1A2CYP2C19L3MBTL1
Hydrochloric Acid SCHEMBL6292095 0.80 KMT2A (0.48) KMT2ASMN1; SMN2CYP1A2CYP2C19L3MBTL1
Oxalic Acid SCHEMBL6726418 0.78 ALDH1A1 (0.50) KMT2ASMN1; SMN2CYP1A2CYP2C19L3MBTL1
SCHEMBL4772789 0.77 METAP1 (0.42) KMT2ASMN1; SMN2CYP1A2CYP2C19L3MBTL1
SCHEMBL6292035 0.75 MAPT (0.45) KMT2ASMN1; SMN2CYP1A2CYP2C19L3MBTL1

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