SCHEMBL18330199

SCHEMBL18330199

C[C@@H]1OCC2(CCN(C(=O)OC(C)(C)C)CC2)C1O

nearest known ligand 0.45

Predicted protein targets (top 11)

geneUniProtsupporting neighboursconfidence
▸ USP2 O75604 1/20 0.45
▸ SMN1; SMN2 Q16637 1/20 0.45
▸ GPR119 Q8TDV5 3/20 0.41
▸ RECQL P46063 1/20 0.41
▸ KDM4E B2RXH2 1/20 0.40
▸ MAPT P10636 1/20 0.40
▸ THRB P10828 1/20 0.40
▸ HPGD P15428 1/20 0.40
▸ NAMPT P43490 7/20 0.39
▸ EPHX2 P34913 1/20 0.39
▸ EPHX1 P07099 1/20 0.38

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
SCHEMBL21952178 1.00 USP2 (0.45) USP2SMN1; SMN2GPR119RECQLKDM4E
SCHEMBL30295739 1.00 USP2 (0.45) USP2SMN1; SMN2GPR119RECQLKDM4E
SCHEMBL26822575 1.00 USP2 (0.45) USP2SMN1; SMN2GPR119RECQLKDM4E
SCHEMBL38665956 1.00 USP2 (0.45) USP2SMN1; SMN2GPR119RECQLKDM4E
SCHEMBL23172919 0.85 USP2 (0.44) USP2SMN1; SMN2GPR119RECQLHPGD
SCHEMBL38665118 0.84 USP2 (0.43) USP2SMN1; SMN2GPR119RECQLKDM4E
SCHEMBL19735994 0.84 USP2 (0.43) USP2SMN1; SMN2GPR119RECQLKDM4E
SCHEMBL30626319 0.81 USP2 (0.40) USP2SMN1; SMN2GPR119RECQLHPGD
SCHEMBL30626326 0.81 USP2 (0.40) USP2SMN1; SMN2GPR119RECQLHPGD
SCHEMBL38666559 0.80 USP2 (0.40) USP2SMN1; SMN2GPR119RECQLKDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20260102394-A1 PYRAZOLO[3,4-B]PYRAZINE SHP2 PHOSPHATASE INHIBITORS OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2026-04-16 — — US disclosed
US-12458640-B2 Pyrazolo[3,4-b]pyrazine SHP2 phosphatase inhibitors OTSUKA PHARMACEUTICAL CO., LTD. (JP) 2025-11-04 — — US disclosed
CN-114206885-B Pyrazolo [3,4-B ] pyrazines SHP2 phosphatase inhibitors 大冢制药株式会社 2025-05-02 — — CN disclosed
EP-4499648-A1 PROCESS FOR PREPARING SHP2 INHIBITORS GENZYME CORPORATION (US) 2025-02-05 — — EP disclosed
US-20250034160-A1 Process For Preparing SHP2 Inhibitors GENZYME CORPORATION (US) 2025-01-30 — — US disclosed
CN-114981268-B Pyrimidine-4 (3H) -ketone heterocyclic compound, preparation method and application thereof in medicine 北京诺诚健华医药科技有限公司 2025-01-28 — — CN disclosed
CN-112513050-B Heterocyclic compounds which inhibit SHP2 activity 大鹏药品工业株式会社 2024-12-20 — — CN disclosed
CN-112625028-B Compounds and compositions for inhibiting SHP2 activity 诺华股份有限公司 2024-10-29 — — CN disclosed
CN-118871443-A Method for preparing SHP2 inhibitor 建新公司 2024-10-29 — — CN disclosed
EP-3630770-B1 PYRAZOLO[3,4-B]PYRAZINE DERIVATIVES AS SHP2 PHOSPHATASE INHIBITORS RELAY THERAPEUTICS INC (US) 2024-08-28 — — EP disclosed
US-10336774-B2 N-azaspirocycloalkane substituted N-heteroaryl compounds and compositions for inhibiting the activity of SHP2 NOVARTIS AG (CH) 2019-07-02 — — US disclosed
US-20190185475-A1 COMPOUNDS AND COMPOSITIONS FOR INHBITING THE ACTIVITY OF SHP2 NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH INC. 2019-06-20 — — US disclosed
EP-3310779-B1 COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF SHP2 NOVARTIS AG (CH) 2019-05-08 — — EP disclosed
US-20180201623-A1 N-AZASPIROCYCLOALKANE SUBSTITUTED N-HETEROARYL COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF SHP2 NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH INC. 2018-07-19 — — US disclosed
US-20180201623-A1 N-AZASPIROCYCLOALKANE SUBSTITUTED N-HETEROARYL COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF SHP2 NOVARTIS INSTITUTES FOR BIOMEDICAL RESEARCH INC. 2018-07-19 — — US disclosed
US-9938295-B2 — — 2018-04-10 — — US disclosed
US-9938295-B2 — — 2018-04-10 — — US disclosed
US-20170015680-A1 N-AZASPIROCYCLOALKANE SUBSTITUTED N-HETEROARYL COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF SHP2 NOVARTIS AG (CH) 2017-01-19 — — US disclosed
US-20170015680-A1 N-AZASPIROCYCLOALKANE SUBSTITUTED N-HETEROARYL COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF SHP2 NOVARTIS AG (CH) 2017-01-19 — — US disclosed
WO-2016203404-A1 COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF SHP2 NOVARTIS AG (CH) 2016-12-22 — — 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 (7 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-10336774-B2 N-azaspirocycloalkane substituted N-heteroaryl compounds and compositions for inhibiting the activity of SHP2 PTPN5, PTPN1, PTPN7 USP2 1924/4885SMN1; SMN2 2598/4885GPR119 1069/4885
US-12458640-B2 Pyrazolo[3,4-b]pyrazine SHP2 phosphatase inhibitors PTPN5, PTPRZ1, PTPN1 USP2 2048/4885SMN1; SMN2 3093/4885GPR119 1866/4885
US-20180201623-A1 N-AZASPIROCYCLOALKANE SUBSTITUTED N-HETEROARYL COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF SHP2 PTPN5, PTPN1, PTPN7 USP2 1924/4885SMN1; SMN2 2598/4885GPR119 1069/4885
US-20190185475-A1 COMPOUNDS AND COMPOSITIONS FOR INHBITING THE ACTIVITY OF SHP2 PTPN1, PTPN3, PTPN5 USP2 3908/4885SMN1; SMN2 3724/4885GPR119 604/4885
US-20260102394-A1 PYRAZOLO[3,4-B]PYRAZINE SHP2 PHOSPHATASE INHIBITORS PTPN5, PTPN1, PTPN3 USP2 2101/4885SMN1; SMN2 2037/4885GPR119 2016/4885
US-20170015680-A1 N-AZASPIROCYCLOALKANE SUBSTITUTED N-HETEROARYL COMPOUNDS AND COMPOSITIONS FOR INHIBITING THE ACTIVITY OF SHP2 PTPN5, PTPN1, PTPN7 USP2 1924/4885SMN1; SMN2 2598/4885GPR119 1069/4885
US-20250034160-A1 Process For Preparing SHP2 Inhibitors PTPN7, PTPRCAP, PTPN18 USP2 491/4885SMN1; SMN2 3016/4885GPR119 1610/4885

“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.

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