SCHEMBL797545

SCHEMBL797545

c1nc(NC2CC2)c2nc[nH]c2n1

nearest known ligand 0.51

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
LMNA P02545 3/20 0.51
HTT P42858 3/20 0.51
PAK1 Q13153 1/20 0.51
PKM P14618 2/20 0.50
HSD17B10 Q99714 1/20 0.50
HPGDS O60760 2/20 0.47
CYP1A2 P05177 1/20 0.45
CYP3A4 P08684 1/20 0.45
CYP2D6 P10635 1/20 0.45
NFKB1 P19838 1/20 0.45
ADORA1 P30542 1/20 0.45
THPO P40225 1/20 0.45
PMP22 Q01453 1/20 0.45
IRAK4 Q9NWZ3 7/20 0.44
JAK2 O60674 4/20 0.42
JAK1 P23458 4/20 0.42
EGFR P00533 1/20 0.41

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
SCHEMBL30473749 1.00 LMNA (0.51) LMNAHTTPAK1PKMHSD17B10
SCHEMBL9205078 0.93 LMNA (0.56) LMNAHTTPAK1PKMHSD17B10
SCHEMBL5452621 0.93 LMNA (0.60) LMNAHTTPAK1PKMHSD17B10
SCHEMBL5458071 0.92 LMNA (0.61) LMNAHTTPAK1PKMHSD17B10
SCHEMBL797230 0.92 LMNA (0.61) LMNAHTTPAK1PKMHSD17B10
SCHEMBL5670409 0.90 RPS6KB1 (0.48) LMNAHTTPAK1PKMHSD17B10
Hydrochloric Acid SCHEMBL1748687 0.89 RPS6KB1 (0.47) LMNAHTTPAK1PKMHSD17B10
SCHEMBL6643407 0.81 GBA1 (0.39) LMNAHTTPAK1HPGDS
SCHEMBL133156 0.78 CHUK (0.45) LMNAHTTPAK1PKMHSD17B10
SCHEMBL30590050 0.78 CHUK (0.45) LMNAHTTPAK1PKMHSD17B10

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20140303112-A1 Method for treating disease or condition susceptible to amelioration by AMPK activators and compounds of formula which are useful to activate AMP-activated protein kinase (AMPK) ENERGENESIS BIOMEDICAL CO., LTD (TW) 2014-10-09 US claimed
US-20260035403-A1 NUCLEOSIDE LINE-1 INHIBITORS TRANSPOSON THERAPEUTICS, INC. (US) 2026-02-05 US disclosed
CN-119278043-A Nucleoside LINE-1 inhibitors 转位治疗股份有限公司 2025-01-07 CN disclosed
WO-2023192491-A2 NUCLEOSIDE LINE-1 INHIBITORS TRANSPOSON THERAPEUTICS, INC. (US) 2023-10-05 WO disclosed
US-20210338706-A1 ADENOSINE ANALOG AND ITS USE IN REGULATING THE CIRCADIAN CLOCK NATIONAL INSTITUTE OF BIOLOGICAL SCIENCES, BEIJING (CN) 2021-11-04 US disclosed
EP-2427195-B1 HETEROCYCLIC COMPOUNDS AND USES THEREOF INTELLIKINE LLC (US) 2019-05-01 EP disclosed
EP-3040337-B1 2, 6-DI-NITROGEN-CONTAINING SUBSTITUTED PURINE DERIVATIVE, AND PREPARATION METHOD, PHARMACEUTICAL COMPOSITION AND USE THEREOF ZHEJIANG MED XINCHANG PHARM (CN) 2019-04-17 EP disclosed
CN-104418858-B Nitrogenous substituted purine derivative of 2,6- bis- and preparation method thereof and its pharmaceutical composition and application 浙江医药股份有限公司新昌制药厂 2018-12-11 CN disclosed
WO-2018133835-A1 NUCLEOSIDE ANALOGUE REGULATING MAMMALIAN CIRCADIAN RHYTHM NATIONAL INSTITUTE OF BIOLOGICAL SCIENCES, BEIJING (CN) 2018-07-26 WO disclosed
WO-2018133854-A1 ADENOSINE ANALOG AND ITS USE IN REGULATING THE CIRCADIAN CLOCK NATIONAL INSTITUTE OF BIOLOGICAL SCIENCES, BEIJING (CN) 2018-07-26 WO disclosed
US-5420115-A Method for the treatment of protoza infections with 21 -deoxy-21 -fluoropurine nucleosides BURROUGHS WELLCOME CO. (US) 1995-05-30 US disclosed
EP-0286425-B1 Therapeutic nucleosides WELLCOME FOUND (GB) 1995-01-11 EP disclosed
US-5185437-A 6-substituted 2',3'-dideoxypurine nucleosides; treatment for human immunodeficiency virus and heptatis b virus BURROUGHS WELLCOME CO. (US) 1993-02-09 US disclosed
US-5068320-A 2-amino-6-(cyclopropylamino)purine-9-β-D-2',3'-dideoxyribofuranoside and its pharmaceutically acceptable salts BURROUGHS WELLCOME CO. (US) 1991-11-26 US disclosed
EP-0421819-A1 Therapeutic nucleosides THE WELLCOME FOUNDATION LIMITED (GB) 1991-04-10 EP disclosed
EP-0417999-A1 Antiviral compounds THE WELLCOME FOUNDATION LIMITED (GB) 1991-03-20 EP disclosed
EP-0366287-A1 Therapeutic nucleosides THE WELLCOME FOUNDATION LIMITED (GB) 1990-05-02 EP disclosed
EP-0317128-A2 Anti-HIV Pyrimidine Nucleosides THE WELLCOME FOUNDATION LIMITED (GB) 1989-05-24 EP disclosed
EP-0294114-A2 Antiviral compounds THE WELLCOME FOUNDATION LIMITED (GB) 1988-12-07 EP disclosed
EP-0286425-A2 Therapeutic nucleosides THE WELLCOME FOUNDATION LIMITED (GB) 1988-10-12 EP 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-20140303112-A1 Method for treating disease or condition susceptible to amelioration by AMPK activators and compounds of formula which are useful to activate AMP-activated protein kinase (AMPK) PRKAG2, PRKAB2, PRKAG1 LMNA 599/4885HTT 3291/4885PAK1 197/4885
US-20260035403-A1 NUCLEOSIDE LINE-1 INHIBITORS L3MBTL1, TDP1, TRDMT1 LMNA 71/4885HTT 214/4885PAK1 2953/4885
US-20210338706-A1 ADENOSINE ANALOG AND ITS USE IN REGULATING THE CIRCADIAN CLOCK PER2, CRY1, ADORA2A LMNA 2993/4885HTT 4069/4885PAK1 3069/4885

“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.