SCHEMBL254870

SCHEMBL254870

O=C(c1ccccc1)N1CCCC1

nearest known ligand 0.96

Predicted protein targets (top 10)

geneUniProtsupporting neighboursconfidence
HPGD P15428 8/20 0.96
ALDH1A1 P00352 3/20 0.81
USP2 O75604 1/20 0.81
MAPK1 P28482 1/20 0.78
SIGMAR1 Q99720 1/20 0.68
L3MBTL1 Q9Y468 2/20 0.68
L3MBTL3 Q96JM7 1/20 0.68
LMNA P02545 1/20 0.68
ACHE P22303 1/20 0.63
BLM P54132 1/20 0.61

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
SCHEMBL18228404 1.00 HPGD (0.96) HPGDALDH1A1USP2MAPK1SIGMAR1
SCHEMBL1927946 0.98 HPGD (1.00) HPGDALDH1A1USP2MAPK1SIGMAR1
SCHEMBL436090 0.98 HPGD (1.00) HPGDALDH1A1USP2MAPK1SIGMAR1
SCHEMBL243236 0.98 HPGD (1.00) HPGDALDH1A1USP2MAPK1SIGMAR1
SCHEMBL8919062 0.98 HPGD (1.00) HPGDALDH1A1USP2MAPK1SIGMAR1
SCHEMBL27929296 0.98 HPGD (1.00) HPGDALDH1A1USP2MAPK1SIGMAR1
Bicarbonate SCHEMBL1582960 0.96 HPGD (0.96) HPGDALDH1A1USP2MAPK1SIGMAR1
Hydrochloric Acid SCHEMBL9209631 0.96 HPGD (0.96) HPGDALDH1A1USP2MAPK1SIGMAR1
SCHEMBL1263133 0.95 HPGD (0.88) HPGDALDH1A1USP2MAPK1SIGMAR1
SCHEMBL2614241 0.93 HPGD (0.84) HPGDALDH1A1USP2MAPK1SIGMAR1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-119798265-A Asymmetric synthetic pyrrole method for preparing lixivium alkaloid 武汉大学深圳研究院 2025-04-11 CN claimed
CN-114805107-A N-alpha position arylation method of nitrogen-containing heterocycle realized by photocatalysis 哈尔滨工业大学(深圳) 2022-07-29 CN claimed
US-11279687-B2 Compounds and compositions for the inhibition of NAMPT VALO HEALTH, INC. (US) 2022-03-22 US claimed
EP-2626358-B1 Immunoassay for pyrrolidinophenones RANDOX LAB LTD (GB) 2015-09-02 EP claimed
US-20130210167-A1 IMMUNOASSAY FOR PYRROLIDINOPHENONES RANDOX LABORATORIES LIMITED (GB) 2013-08-15 US claimed
EP-2626358-A1 Immunoassay for pyrrolidinophenones Randox Laboratories Ltd. (GB) 2013-08-14 EP claimed
US-20100160305-A1 3, 4, 5 - Substituted Piperidine Compounds NOVARTIS AG (CH) 2010-06-24 US claimed
US-20100029647-A1 3,4,(5)-SUBSTITUTED TETRAHYDROPHYRIDINES NOVARTIS AG (CH) 2010-02-04 US claimed
US-20080194629-A1 3-Mono-and 3,5-Disubstituted Piperidine Derivatives as Renin Inhibitors BAESCHLIN DANIEL KASPAR 2008-08-14 US claimed
EP-1915366-A2 PIPERAZINE DERIVATIVE RENIN INHIBITORS Novartis AG (CH) 2008-04-30 EP claimed
EP-1841740-A1 3,4,(5)-SUBSTITUTED TETRAHVDROPYRIDINES Novartis AG (CH) 2007-10-10 EP claimed
US-20070232673-A1 2-Imino-benzimidazoles ABBOTT LABORATORIES 2007-10-04 US claimed
WO-2006128659-A2 PIPERAZINE DERIVATIVE RENIN INHIBITORS. NOVARTIS AG (CH) 2006-12-07 WO claimed
WO-2006117183-A1 3 -M0N0- AND 3 , 5-DISUBSTITUTED PIPERIDINE DERIVATIVES AS RENIN INHIBITORS NOVARTIS AG (CH) 2006-11-09 WO claimed
WO-2006094763-A1 3,4,5-SUBSTITUTED PIPERIDINE COMPOUNDS NOVARTIS AG (CH) 2006-09-14 WO claimed
WO-2006074924-A1 3,4,(5)-SUBSTITUTED TETRAHVDROPYRIDINES NOVARTIS AG (CH) 2006-07-20 WO claimed
WO-2006034196-A1 COMPOSITIONS FOR ENHANCING MEMORY AND METHODS THEREFOR LIFELIKE BIOMATIC INC. (US) 2006-03-30 WO claimed
US-20060063707-A1 Compositions for enhancing memory and methods therefor LIFELIKE BIOMATIC, INC. (US) 2006-03-23 US claimed
US-5496844-A Indole derivatives OTSUKA PHARMACEUTICAL FACTORY, INC. (JP) 1996-03-05 US claimed
EP-0639567-A1 INDOLE DERIVATIVE OTSUKA PHARMACEUTICAL FACTORY, INC. (JP) 1995-02-22 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (6 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-20060063707-A1 Compositions for enhancing memory and methods therefor GRIN1, GRIN3A, GRIN2A HPGD 1202/4885ALDH1A1 4321/4885USP2 3620/4885
US-11279687-B2 Compounds and compositions for the inhibition of NAMPT NAMPT, NNT, NQO1 HPGD 199/4885ALDH1A1 511/4885USP2 4856/4885
US-20100029647-A1 3,4,(5)-SUBSTITUTED TETRAHYDROPHYRIDINES REN, PAH, ACE HPGD 113/4885ALDH1A1 412/4885USP2 4728/4885
US-20070232673-A1 2-Imino-benzimidazoles CYP2C19, UGT2B7, UGT2B17 HPGD 501/4885ALDH1A1 39/4885USP2 4413/4885
US-20080194629-A1 3-Mono-and 3,5-Disubstituted Piperidine Derivatives as Renin Inhibitors REN, ACE, AGTR1 HPGD 435/4885ALDH1A1 231/4885USP2 3632/4885
US-20100160305-A1 3, 4, 5 - Substituted Piperidine Compounds REN, ACE, PIGO HPGD 309/4885ALDH1A1 56/4885USP2 3887/4885

“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.