SCHEMBL1624629

SCHEMBL1624629

Cc1cc(C)c(N)c(Nc2ccc(CCO)cc2)n1

nearest known ligand 0.51

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.51
KMT2A Q03164 1/20 0.51
CDC7 O00311 1/20 0.39
ALK Q9UM73 1/20 0.39
RAB9A P51151 2/20 0.39
NPC1 O15118 1/20 0.39
ALDH1A1 P00352 5/20 0.39
KDM4E B2RXH2 5/20 0.39
HPGD P15428 5/20 0.39
HSD17B10 Q99714 3/20 0.39
SMN1; SMN2 Q16637 1/20 0.39
AGPAT2 O15120 1/20 0.39
FCGR3B O75015 1/20 0.39
FCGR1A P12314 1/20 0.39
FCGR2A P12318 1/20 0.39
GAA P10253 2/20 0.39
CDK1 P06493 2/20 0.37
KDR P35968 2/20 0.37
PDE4B Q07343 2/20 0.37
MAPK1 P28482 1/20 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
SCHEMBL7169031 0.92 MEN1 (0.49) MEN1KMT2ARAB9ANPC1ALDH1A1
SCHEMBL7017813 0.87 MEN1 (0.49) MEN1KMT2ARAB9ANPC1ALDH1A1
SCHEMBL1625684 0.86 AGPAT2 (0.42) MEN1KMT2ACDC7ALKALDH1A1
SCHEMBL3950718 0.83 KMT2A (0.50) MEN1KMT2ARAB9ANPC1ALDH1A1
SCHEMBL1625442 0.82 MEN1 (0.50) MEN1KMT2ARAB9ANPC1ALDH1A1
SCHEMBL1625505 0.81 MEN1 (0.49) MEN1KMT2ARAB9ANPC1ALDH1A1
SCHEMBL1626147 0.81 MEN1 (0.49) MEN1KMT2ARAB9ANPC1ALDH1A1
SCHEMBL1623514 0.80 MEN1 (0.41) MEN1KMT2ACDC7ALKRAB9A
SCHEMBL1626044 0.79 CDC7 (0.40) MEN1KMT2ACDC7ALKALDH1A1
SCHEMBL1624553 0.79 PDE4B (0.40) MEN1KMT2ARAB9ANPC1AGPAT2

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 35 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-106745722-A A kind of mobile tunnel type anaerobic pond support meanss and its method of work 徐州工程学院 2017-05-31 CN claimed
CN-106745722-B Mobile tunnel type anaerobic tank supporting device and working method thereof 徐州腾睿智能装备有限公司 2020-09-15 CN disclosed
CN-106745722-A A kind of mobile tunnel type anaerobic pond support meanss and its method of work 徐州工程学院 2017-05-31 CN disclosed
EP-1666480-B1 Aryl or Heteroaryl Fused Imidazole Compounds as intermediates for Anti-Inflammatory And Analgesic Agents. RAQUALIA PHARMA INC (JP) 2014-10-01 EP disclosed
US-7960407-B2 Crystal forms of an imidazole derivative REQUALIA PHARMA INC. (JP) 2011-06-14 US disclosed
US-7928119-B2 Use of EP4 receptor ligands in the treatment of IL-6 involved diseases PFIZER INC. (US) 2011-04-19 US disclosed
CN-101137656-B Crystal forms of imidazole derivatives PFIZER JAPAN INC 2010-12-22 CN disclosed
EP-1861400-B1 CRYSTAL FORMS OF AN IMIDAZOLE DERIVATIVE RAQUALIA PHARMA INC (JP) 2010-05-26 EP disclosed
WO-2005102389-A9 COMBINATIONS COMPRISING ALPHA-2-DELTA LIGANDS AND EP4 RECEPTOR ANTAGONISTS PFIZER PROD INC (US) 2009-04-30 WO disclosed
US-20090036495-A1 Combinations Comprising Alpha-2-Delta Ligands and Ep4 Receptor Antagonists PFIZER, INC. 2009-02-05 US disclosed
US-6710054-B2 CONTAINING SULFONYLAMINOCARBONYL GROUPS; PROSTAGLANDIN INHIBITORS PFIZER INC 2004-03-23 US disclosed
CN-1476448-A Aryl or heteroaryl fused imidazole compounds as anti-inflammatory and analgesic agents ������ҩ�����޹�˾ 2004-02-18 CN disclosed
US-20030236260-A1 Use of EP4 receptor ligands in the treatment of IL-6 involved diseases SHIMOJO MASATO 2003-12-25 US disclosed
WO-2003086371-A2 USE OF EP4 RECEPTOR LIGANDS IN THE TREATMENT OF IL-6 INVOLVED DISEASES PFIZER JAPAN INC. (JP) 2003-10-23 WO disclosed
EP-1326864-A2 ARYL OR HETEROARYL FUSED IMIDAZOLE COMPOUNDS AS ANTI-INFLAMMATORY AND ANALGESIC AGENTS PFIZER PHARMACEUTICALS INC. (JP) 2003-07-16 EP disclosed
EP-1326606-A2 EP4 RECEPTOR INHIBITORS TO TREAT RHEUMATOID ARTHRITIS PFIZER PHARMACEUTICALS INC. (JP) 2003-07-16 EP disclosed
US-20020107273-A1 Aryl or heteroaryl fused imidazole compounds as anti-inflammatory and analgesic agents ASKAT INC. (JP) 2002-08-08 US disclosed
US-20020077329-A1 EP4 receptor inhibitors to treat rheumatoid arthritis PFIZER PHARMACEUTICALS INC. (JP) 2002-06-20 US disclosed
WO-2002032422-A2 EP4 RECEPTOR INHIBITORS TO TREAT RHEUMATOID ARTHRITIS PFIZER PHARMACEUTICALS INC. (JP) 2002-04-25 WO disclosed
WO-2002032900-A2 ARYL OR HETEROARYL FUSED IMIDAZOLE COMPOUNDS AS ANTI-INFLAMMATORY AND ANALGESIC AGENTS PFIZER PHARMACEUTICALS INC. (JP) 2002-04-25 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 (4 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-20020107273-A1 Aryl or heteroaryl fused imidazole compounds as anti-inflammatory and analgesic agents PTGS1, PTGS2, OPRM1 MEN1 3912/4885KMT2A 2917/4885CDC7 4230/4885
US-20030236260-A1 Use of EP4 receptor ligands in the treatment of IL-6 involved diseases PTGER4, PTGER1, IL6 MEN1 4475/4885KMT2A 4355/4885CDC7 4334/4885
US-20020077329-A1 EP4 receptor inhibitors to treat rheumatoid arthritis PTGER4, PTGER1, PTGER2 MEN1 4826/4885KMT2A 3764/4885CDC7 4194/4885
US-20090036495-A1 Combinations Comprising Alpha-2-Delta Ligands and Ep4 Receptor Antagonists PTGER4, PTGER2, OPRL1 MEN1 4563/4885KMT2A 2227/4885CDC7 4582/4885

“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.