SCHEMBL14703477

SCHEMBL14703477

N=C(NCCc1ccccc1)NC(=N)N1CCCC1

nearest known ligand 0.58

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ NPC1 O15118 8/20 0.58
▸ RAB9A P51151 6/20 0.58
▸ SMN1; SMN2 Q16637 4/20 0.58
▸ HTT P42858 1/20 0.58
▸ GAA P10253 3/20 0.53
▸ TAAR1 Q96RJ0 1/20 0.49
▸ ALDH1A1 P00352 2/20 0.46
▸ DPP4 P27487 1/20 0.45
▸ TDP1 Q9NUW8 1/20 0.45
▸ SIGMAR1 Q99720 1/20 0.44
▸ KMT2A Q03164 3/20 0.44
▸ MEN1 O00255 2/20 0.44
▸ NPSR1 Q6W5P4 1/20 0.44
▸ LMNA P02545 1/20 0.44
▸ MAPT P10636 1/20 0.44

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
SCHEMBL14703378 0.99 NPC1 (0.61) NPC1RAB9ASMN1; SMN2HTTGAA
Hydrochloric Acid SCHEMBL17668295 0.99 NPC1 (0.57) NPC1RAB9ASMN1; SMN2HTTGAA
SCHEMBL14703148 0.99 NPC1 (0.61) NPC1RAB9ASMN1; SMN2HTTGAA
Hydrochloric Acid SCHEMBL17668293 0.97 NPC1 (0.59) NPC1RAB9ASMN1; SMN2HTTGAA
Hydrochloric Acid SCHEMBL17668288 0.97 NPC1 (0.59) NPC1RAB9ASMN1; SMN2HTTGAA
SCHEMBL16692416 0.86 MCHR1 (0.48) NPC1RAB9ASMN1; SMN2HTTTAAR1
SCHEMBL14703383 0.85 MCHR1 (0.50) NPC1RAB9ASMN1; SMN2HTTGAA
SCHEMBL19393790 0.85 NPC1 (0.45) NPC1RAB9ASMN1; SMN2HTTGAA
SCHEMBL17777313 0.85 MCHR1 (0.50) NPC1RAB9ASMN1; SMN2HTTGAA
SCHEMBL14703253 0.85 TSHR (0.50) NPC1RAB9ASMN1; SMN2HTTGAA

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 NPC1 308/4885RAB9A 1508/4885SMN1; SMN2 3229/4885

“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.

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