SCHEMBL3289909

SCHEMBL3289909

CC(=O)Cl.c1ccc(-c2ccc(C3CCCCC3)cc2)cc1

nearest known ligand 0.58

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 1/20 0.58
RAB9A P51151 1/20 0.58
SLC6A2 P23975 1/20 0.51
SLC6A4 P31645 1/20 0.51
DHODH Q02127 1/20 0.49
HAO1 Q9UJM8 1/20 0.45
KMO O15229 1/20 0.45
CYP3A4 P08684 2/20 0.45
CYP2C9 P11712 1/20 0.45
APP P05067 1/20 0.45
KMT2A Q03164 2/20 0.44
SMN1; SMN2 Q16637 2/20 0.44
TDP1 Q9NUW8 2/20 0.44
KDM4E B2RXH2 1/20 0.44
GLA P06280 1/20 0.44
HTT P42858 1/20 0.44
HIF1A Q16665 1/20 0.44
L3MBTL1 Q9Y468 1/20 0.44
ACMSD Q8TDX5 1/20 0.44
HDAC1 Q13547 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
Bicarbonate SCHEMBL27623769 0.90 NPC1 (0.66) NPC1RAB9ASLC6A2SLC6A4DHODH
SCHEMBL27848727 0.86 NPC1 (0.58) NPC1RAB9ASLC6A2SLC6A4DHODH
SCHEMBL537001 0.86 NPC1 (0.58) NPC1RAB9ASLC6A2SLC6A4DHODH
SCHEMBL18561699 0.86 NPC1 (0.58) NPC1RAB9ASLC6A2SLC6A4DHODH
SCHEMBL15758248 0.84 NPC1 (0.60) NPC1RAB9ASLC6A2SLC6A4DHODH
Acetone SCHEMBL28117313 0.82 KMO (0.58) HAO1KMOCYP2C9KMT2ASMN1; SMN2
SCHEMBL11290635 0.82 KMO (0.58) NPC1RAB9ADHODHHAO1KMO
Fluoride SCHEMBL28559395 0.82 NPC1 (0.58) NPC1RAB9ASLC6A2SLC6A4DHODH
Hydrogen Peroxide SCHEMBL28451101 0.82 NPC1 (0.52) NPC1RAB9ADHODHHAO1KMO
SCHEMBL28751412 0.81 NPC1 (0.54) NPC1RAB9ASLC6A2SLC6A4DHODH

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-8404731-B2 Substituted imidazole derivatives, compositions, and methods of use as PTPase inhibitors TRANSTECH PHARMA, INC. (US) 2013-03-26 US disclosed
US-20120196906-A1 Substituted Imidazole Derivatives, Compositions, and Methods of Use as PTPase Inhibitors TRANSTECH PHARMA, INC. (US) 2012-08-02 US disclosed
CN-101374835-B Substituted imidazole derivatives, compositions, and methods of use as PTPase inhibitors TRANSTECH PHARMA INC 2012-04-25 CN disclosed
US-7723369-B2 Substituted imidazole derivatives, compositions, and methods of use as PTPase inhibitors TRANSTECH PHARMA, INC. (US) 2010-05-25 US disclosed
US-20100113331-A1 Substituted Imidazole Derivatives, Compositions, and Methods of Use as PtPase Inhibitors TRANSTECH PHARMA, INC. (US) 2010-05-06 US disclosed
CN-101374835-A Substituted imidazole derivatives, compositions, and methods of use as PTPase inhibitors TRANSTECH PHARMA INC (US) 2009-02-25 CN disclosed
EP-1991544-A2 SUBSTITUTED IMIDAZOLE DERIVATIVES AND THEIR USE AS PTPASE INHIBITORS Transtech Pharma, Inc. (US) 2008-11-19 EP disclosed
US-20070191385-A1 Substituted imidazole derivatives, compositions, and methods of use as PTPase inhibitors VTV THERAPEUTICS LLC 2007-08-16 US disclosed
WO-2007089857-A2 SUBSTITUTED IMIDAZOLE DERIVATIVES AND THEIR USE AS PTPASE INHIBITORS TRANSTECH PHARMA, INC. (US) 2007-08-09 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 (3 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-20070191385-A1 Substituted imidazole derivatives, compositions, and methods of use as PTPase inhibitors PTP4A1, PTPRJ, PTP4A2 NPC1 2905/4885RAB9A 2481/4885SLC6A2 2934/4885
US-20100113331-A1 Substituted Imidazole Derivatives, Compositions, and Methods of Use as PtPase Inhibitors PTP4A1, PTPRJ, PTP4A2 NPC1 2905/4885RAB9A 2481/4885SLC6A2 2934/4885
US-20120196906-A1 Substituted Imidazole Derivatives, Compositions, and Methods of Use as PTPase Inhibitors PTP4A1, PTPRJ, PTP4A2 NPC1 2905/4885RAB9A 2481/4885SLC6A2 2934/4885

“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.