SCHEMBL1376362

SCHEMBL1376362

Cc1ccccc1OP(Oc1ccccc1C)Oc1ccccc1C.[Ni]

nearest known ligand 0.45

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
TSHR P16473 3/20 0.45
NPC1 O15118 2/20 0.45
RAB9A P51151 2/20 0.45
SMN1; SMN2 Q16637 2/20 0.45
MEN1 O00255 1/20 0.45
KMT2A Q03164 1/20 0.45
ACHE P22303 1/20 0.43
ALDH1A1 P00352 2/20 0.39
GLA P06280 1/20 0.39
CYP1A2 P05177 2/20 0.38
KDM4E B2RXH2 1/20 0.38
HPGD P15428 2/20 0.38
CA12 O43570 1/20 0.38
CA1 P00915 1/20 0.38
CA2 P00918 1/20 0.38
CA4 P22748 1/20 0.38
CA7 P43166 1/20 0.38
CA9 Q16790 1/20 0.38
CA14 Q9ULX7 1/20 0.38
SCN4A P35499 2/20 0.37

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
SCHEMBL11864172 1.00 TSHR (0.45) TSHRNPC1RAB9ASMN1; SMN2MEN1
SCHEMBL10706430 1.00 TSHR (0.45) TSHRNPC1RAB9ASMN1; SMN2MEN1
SCHEMBL27387712 0.97 TSHR (0.46) TSHRNPC1RAB9ASMN1; SMN2MEN1
SCHEMBL215848 0.97 TSHR (0.46) TSHRNPC1RAB9ASMN1; SMN2MEN1
SCHEMBL29405565 0.97 TSHR (0.46) TSHRNPC1RAB9ASMN1; SMN2MEN1
SCHEMBL11818909 0.95 TSHR (0.45) TSHRNPC1RAB9ASMN1; SMN2MEN1
SCHEMBL27491899 0.95 TSHR (0.45) TSHRNPC1RAB9ASMN1; SMN2MEN1
Hydrochloric Acid SCHEMBL10779050 0.95 TSHR (0.45) TSHRNPC1RAB9ASMN1; SMN2MEN1
SCHEMBL27476174 0.95 TSHR (0.45) TSHRNPC1RAB9ASMN1; SMN2MEN1
SCHEMBL27524236 0.95 TSHR (0.45) TSHRNPC1RAB9ASMN1; SMN2MEN1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-111892514-A Method for preparing adiponitrile by direct hydrocyanation of butadiene 阳泉煤业(集团)有限责任公司 2020-11-06 CN disclosed
US-8772527-B2 Process for isomerization of cis-2-pentenenitrile to 3-pentenenitriles BASF SE (DE) 2014-07-08 US disclosed
US-20130289299-A1 Process for Isomerization of CIS-2-Pentenenitrile to 3-Pentenenitriles BASF SE (DE) 2013-10-31 US disclosed
US-8530690-B2 Process for isomerizing CIS-2-pentenenitrile to 3-pentenenitriles BASF SE (DE) 2013-09-10 US disclosed
US-20110288326-A1 PROCESS FOR ISOMERIZING CIS-2-PENTENENITRILE TO 3-PENTENENITRILES BASF SE (DE) 2011-11-24 US 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-20110288326-A1 PROCESS FOR ISOMERIZING CIS-2-PENTENENITRILE TO 3-PENTENENITRILES PARN, CPNE4, AAAS TSHR 3145/4885NPC1 3583/4885RAB9A 1803/4885
US-20130289299-A1 Process for Isomerization of CIS-2-Pentenenitrile to 3-Pentenenitriles PORCN, PIN1, ORAI2 TSHR 4507/4885NPC1 2807/4885RAB9A 4628/4885

“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.