SCHEMBL14703141

SCHEMBL14703141

N=C(NCc1ccc(Cl)c(Cl)c1)NC(=N)N1CCCC1

nearest known ligand 0.48

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
▸ EPHX2 P34913 1/20 0.48
▸ HRH3 Q9Y5N1 3/20 0.47
▸ TSHR P16473 2/20 0.44
▸ SMN1; SMN2 Q16637 3/20 0.43
▸ POLB P06746 2/20 0.43
▸ SIGMAR1 Q99720 3/20 0.41
▸ ALDH1A1 P00352 2/20 0.41
▸ LMNA P02545 1/20 0.41
▸ HPGD P15428 2/20 0.39
▸ MEN1 O00255 2/20 0.39
▸ KMT2A Q03164 2/20 0.39
▸ NPC1 O15118 1/20 0.39
▸ RAB9A P51151 1/20 0.39
▸ ERN1 O75460 1/20 0.39
▸ TAOK1 Q7L7X3 1/20 0.39
▸ TAOK3 Q9H2K8 1/20 0.39

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
SCHEMBL14703147 0.99 EPHX2 (0.47) EPHX2HRH3TSHRSMN1; SMN2POLB
SCHEMBL28487664 0.86 HRH3 (0.45) EPHX2HRH3TSHRSMN1; SMN2POLB
Hydrochloric Acid SCHEMBL18191032 0.85 HRH3 (0.44) EPHX2HRH3TSHRSMN1; SMN2POLB
SCHEMBL14703674 0.85 PHGDH (0.40) EPHX2HRH3SMN1; SMN2ALDH1A1MEN1
SCHEMBL14703437 0.85 ALDH1A1 (0.45) HRH3SMN1; SMN2POLBALDH1A1LMNA
SCHEMBL14703252 0.84 SMN1; SMN2 (0.46) EPHX2SMN1; SMN2ALDH1A1
SCHEMBL14703140 0.83 ALDH1A1 (0.47) HRH3SMN1; SMN2ALDH1A1LMNAHPGD
SCHEMBL14703673 0.83 ALDH1A1 (0.47) HRH3SMN1; SMN2ALDH1A1LMNAHPGD
SCHEMBL919132 0.82 TSHR (0.57) EPHX2HRH3TSHRSMN1; SMN2POLB
SCHEMBL18197821 0.82 HRH3 (0.43) EPHX2HRH3TSHRSMN1; SMN2POLB

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-2742020-B1 N1-CYCLIC AMINE-N5-SUBSTITUTED BIGUANIDE DERIVATIVES, METHODS OF PREPARING THE SAME AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME IMMUNOMET THERAPEUTICS INC (US) 2017-10-25 — — EP disclosed
US-9321742-B2 N1-cyclic amine-N5-substituted biguanide derivatives, methods of preparing the same and pharmaceutical composition comprising the same IMMUNOMET THERAPEUTICS INC. (US) 2016-04-26 — — US disclosed
US-9321742-B2 N1-cyclic amine-N5-substituted biguanide derivatives, methods of preparing the same and pharmaceutical composition comprising the same IMMUNOMET THERAPEUTICS INC. (US) 2016-04-26 — — US disclosed
US-20140179661-A1 N1-Cyclic Amine-N5-Substituted Biguanide Derivatives, Methods of Preparing the Same and Pharmaceutical Composition Comprising the Same HANALL BIOPHARMA CO., LTD. (KR) 2014-06-26 — — US disclosed
US-20140179661-A1 N1-Cyclic Amine-N5-Substituted Biguanide Derivatives, Methods of Preparing the Same and Pharmaceutical Composition Comprising the Same HANALL BIOPHARMA CO., LTD. (KR) 2014-06-26 — — US disclosed
WO-2013022279-A2 N1-CYCLIC AMINE-N5-SUBSTITUTED BIGUANIDE DERIVATIVES, METHODS OF PREPARING THE SAME AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME HANALL BIOPHARMA CO., LTD. (KR) 2013-02-14 — — WO 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-20140179661-A1 N1-Cyclic Amine-N5-Substituted Biguanide Derivatives, Methods of Preparing the Same and Pharmaceutical Composition Comprising the Same PRKAG1, GCKR, GPR119 EPHX2 4387/4885HRH3 3910/4885TSHR 1205/4885

“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.

Send feedback