SCHEMBL4875893

SCHEMBL4875893

CC(C)(C)OC(=O)N1CC2CC(NCc3ccccc3)CC2C1

nearest known ligand 0.54

Predicted protein targets (top 17)

geneUniProtsupporting neighboursconfidence
JAK1 P23458 2/20 0.54
JAK2 O60674 1/20 0.54
NR1H2 P55055 1/20 0.51
STS P08842 1/20 0.47
NAMPT P43490 1/20 0.46
ACHE P22303 1/20 0.46
GPR119 Q8TDV5 2/20 0.45
TACR1 P25103 1/20 0.45
KEAP1 Q14145 1/20 0.45
NFE2L2 Q16236 1/20 0.45
USP30 Q70CQ3 2/20 0.44
LMNA P02545 1/20 0.44
KDM4E B2RXH2 1/20 0.44
PKM P14618 1/20 0.44
RORC P51449 1/20 0.43
KMT2A Q03164 1/20 0.43
L3MBTL1 Q9Y468 1/20 0.43

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
SCHEMBL10320157 1.00 JAK1 (0.54) JAK1JAK2NR1H2STSNAMPT
SCHEMBL22435955 1.00 JAK1 (0.54) JAK1JAK2NR1H2STSNAMPT
SCHEMBL10449417 1.00 JAK1 (0.54) JAK1JAK2NR1H2STSNAMPT
SCHEMBL6269523 0.94 JAK2 (0.50) JAK1JAK2NR1H2STSNAMPT
SCHEMBL10321076 0.92 JAK2 (0.66) JAK1JAK2STSACHEGPR119
SCHEMBL10450116 0.92 JAK2 (0.66) JAK1JAK2STSACHEGPR119
SCHEMBL9937172 0.90 STS (0.50) JAK1JAK2STSNAMPTACHE
SCHEMBL29577032 0.89 JAK2 (0.46) JAK1JAK2STSNAMPTACHE
SCHEMBL21276388 0.89 NR1H2 (0.50) JAK1JAK2NR1H2NAMPTGPR119
SCHEMBL8215310 0.87 CARM1 (0.47) JAK1JAK2NR1H2STSNAMPT

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250115609-A1 AROMATIC HETEROCYCLIC COMPOUNDS, PREPARATION METHOD THEREFOR AND USES THEREOF INNOVSTONE THERAPEUTICS LIMITED (CN) 2025-04-10 US disclosed
EP-4450503-A1 AROMATIC HETEROCYCLIC COMPOUNDS, PREPARATION METHOD THEREFOR AND USES THEREOF Innovstone Therapeutics Limited (CN) 2024-10-23 EP disclosed
CN-118203585-A Pharmaceutical use of ENPP1 inhibitors 上海翊石医药科技有限公司 2024-06-18 CN disclosed
WO-2023109909-A1 AROMATIC HETEROCYCLIC COMPOUNDS, PREPARATION METHOD THEREFOR AND USES THEREOF 上海翊石医药科技有限公司 2023-06-22 WO disclosed
CN-116262750-A Aromatic heterocyclic compound and preparation method and application thereof 上海翊石医药科技有限公司 2023-06-16 CN disclosed
EP-3347097-B1 SUBSTITUTED AMINOPYRIMIDINE DERIVATIVES AS MODULATORS OF THE KINASES JAK, FLT3 AND AURORA SUNSHINE LAKE PHARMA CO LTD (CN) 2021-02-24 EP disclosed
EP-3312164-B1 SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE CALITOR SCIENCES LLC (US) 2020-12-09 EP disclosed
EP-3327006-B1 SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE CALITOR SCIENCES LLC (US) 2020-05-20 EP disclosed
US-10266521-B2 Substituted heteroaryl compounds and methods of use CALITOR SCIENCES, LLC (US) 2019-04-23 US disclosed
EP-3347097-A1 SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE Sunshine Lake Pharma Co., Ltd. (CN) 2018-07-18 EP disclosed
US-20150274705-A1 SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE SUNSHINE LAKE PHARMA CO., LTD. (CN) 2015-10-01 US disclosed
WO-2015148867-A1 SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE CALITOR SCIENCES, LLC (US) 2015-10-01 WO disclosed
WO-2015148868-A1 SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE CALITOR SCIENCES, LLC (US) 2015-10-01 WO disclosed
US-20150274704-A1 SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE SUNSHINE LAKE PHARMA CO., LTD. (CN) 2015-10-01 US disclosed
US-8987442-B2 Deuterium-substituted xanthine derivatives and methods of use CONCERT PHARMACEUTICALS, INC. (US) 2015-03-24 US disclosed
US-7381738-B2 Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity BRISTOL-MYERS SQUIBB COMPANY (US) 2008-06-03 US disclosed
US-7288563-B2 Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity BRISTOL-MYERS SQUIBB COMPANY (US) 2007-10-30 US disclosed
US-20050227960-A1 Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity BRISTOL-MYERS SQUIBB COMPANY 2005-10-13 US disclosed
US-20050192276-A1 Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity BRISTOL-MYERS SQUIBB COMPANY 2005-09-01 US disclosed
WO-2005079519-A2 SUBSTITUTED BICYCLOALKYLAMINE DERIVATIVES AS MODULATORS OF CHEMOKINE RECEPTOR ACTIVITY BRISTOL-MYERS SQUIBB COMPANY (US) 2005-09-01 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 (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-20050192276-A1 Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity CCR1, CCR2, BDKRB1 JAK1 2060/4885JAK2 2048/4885NR1H2 112/4885
US-20150274705-A1 SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE PRKACA, PACSIN2, PRKDC JAK1 299/4885JAK2 205/4885NR1H2 1076/4885
US-20050227960-A1 Substituted bicycloalkylamine derivatives as modulators of chemokine receptor activity CCR1, CCR2, CCR10 JAK1 1897/4885JAK2 1796/4885NR1H2 105/4885
US-10266521-B2 Substituted heteroaryl compounds and methods of use PRKACA, PRKDC, PRKACB JAK1 212/4885JAK2 214/4885NR1H2 1299/4885
US-20250115609-A1 AROMATIC HETEROCYCLIC COMPOUNDS, PREPARATION METHOD THEREFOR AND USES THEREOF ENPP1, WEE1, ENPP2 JAK1 539/4885JAK2 1638/4885NR1H2 2534/4885
US-20150274704-A1 SUBSTITUTED HETEROARYL COMPOUNDS AND METHODS OF USE PRKACA, PRKDC, PRKACB JAK1 278/4885JAK2 240/4885NR1H2 976/4885

“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.