SCHEMBL2906281

SCHEMBL2906281

CC1CCC(N)(C(=O)O)CC1

nearest known ligand 0.64

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
▸ GRM4 Q14833 8/20 0.52
▸ CYP1A2 P05177 4/20 0.52
▸ CYP2C19 P33261 4/20 0.52
▸ GRM2 Q14416 3/20 0.52
▸ GRM3 Q14832 3/20 0.52
▸ ALOX15 P16050 3/20 0.52
▸ TDP1 Q9NUW8 2/20 0.52
▸ GRM8 O00222 2/20 0.52
▸ GRM6 O15303 2/20 0.52
▸ LMNA P02545 1/20 0.52
▸ GRM5 P41594 1/20 0.52
▸ MTOR P42345 1/20 0.52
▸ GRM1 Q13255 1/20 0.52
▸ PLCB1 Q9NQ66 1/20 0.52
▸ TSHR P16473 1/20 0.52
▸ ALDH1A1 P00352 2/20 0.43
▸ CYP2C9 P11712 2/20 0.43
▸ MEN1 O00255 1/20 0.43
▸ KMT2A Q03164 1/20 0.43
▸ CYP2D6 P10635 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
SCHEMBL14372097 1.00 GRM4 (0.52) GRM4CYP1A2CYP2C19GRM2GRM3
SCHEMBL8179890 1.00 GRM4 (0.52) GRM4CYP1A2CYP2C19GRM2GRM3
Hydrochloric Acid SCHEMBL28534660 0.98 GRM4 (0.50) GRM4CYP1A2CYP2C19GRM2GRM3
SCHEMBL31415502 0.92 GRM4 (0.46) GRM4CYP1A2CYP2C19GRM2GRM3
SCHEMBL31415320 0.92 GRM4 (0.46) GRM4CYP1A2CYP2C19GRM2GRM3
SCHEMBL2898361 0.86 GRM4 (0.59) GRM4CYP1A2CYP2C19GRM2GRM3
SCHEMBL912861 0.78 GRM4 (0.54) GRM4CYP1A2CYP2C19GRM2GRM3
SCHEMBL544530 0.78 GRM4 (0.54) GRM4CYP1A2CYP2C19GRM2GRM3
SCHEMBL5007909 0.78 GRM4 (0.54) GRM4CYP1A2CYP2C19GRM2GRM3
SCHEMBL5007910 0.78 GRM4 (0.54) GRM4CYP1A2CYP2C19GRM2GRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-11970495-B2 Indolizine derivatives and their application in medicine KIND PHARMACEUTICAL (CN) 2024-04-30 — — US disclosed
US-11945817-B2 Indolizine derivatives and their application in medicine KIND PHARMACEUTICAL (CN) 2024-04-02 — — US disclosed
US-20230257379-A1 INDOLIZINE DERIVATIVES AND THEIR APPLICATION IN MEDICINE KIND PHARMACEUTICAL (CN) 2023-08-17 — — US disclosed
US-20230242527-A1 INDOLIZINE DERIVATIVES AND THEIR APPLICATION IN MEDICINE KIND PHARMACEUTICAL (CN) 2023-08-03 — — US disclosed
US-11655249-B2 Indolizine derivatives and their application in medicine KIND PHARMACEUTICAL (CN) 2023-05-23 — — US disclosed
WO-2023081730-A1 4-HYDROXY-2-OXO-1,2-DIHYDRO-1,8-NAPHTHYRIDINE-3-CARBOXAMIDE DERIVATIVES AS CANNABINOID CB2 RECEPTOR MODULATORS FOR THE TREATMENT OF CANCER TEON THERAPEUTICS, INC. (US) 2023-05-11 — — WO disclosed
EP-3613742-B1 INDOLIZINE DERIVATIVES AND APPLICATION THEREOF IN MEDICINE KIND PHARMACEUTICAL (CN) 2022-12-07 — — EP disclosed
CN-108727468-B Cyclic peptide, pharmaceutical or cosmetic composition comprising the same, and preparation method thereof 陈建添 2021-12-03 — — CN disclosed
EP-3628677-B1 METHOD FOR PREPARING A CYCLOPEPTIDE UNIV NAT TSING HUA (TW) 2021-11-10 — — EP disclosed
US-20210253570-A1 INDOLIZINE DERIVATIVES AND THEIR APPLICATION IN MEDICINE KIND PHARMACEUTICAL (CN) 2021-08-19 — — US disclosed
US-6140358-A FOR CONTROLLING PESTS AND WEEDS BAYER AKTIENGESELLSCHAFT (DE) 2000-10-31 — — US disclosed
US-5965579-A ANTAGONISTS OF THE NEUROTENSIN RECEPTORS; INCREASING AFFINITY FOR HUMAN NEUROTENSIN RECEPTORS SANOFI (FR) 1999-10-12 — — US disclosed
US-5939449-A NOVEL COMPOUNDS HAVING HIGH AFFINITY FOR THE NEUROTENSIN RECEPTORS SANOFI (FR) 1999-08-17 — — US disclosed
US-5936123-A COMPOUNDS SUCH AS 3-ISOPROPYL-4-HYDRAZINOBENZOIC ACID AND ITS SALTS SANOFI (FR) 1999-08-10 — — US disclosed
US-5925661-A NERVOUS SYSTEM DISORDERS SANOFI (FR) 1999-07-20 — — US disclosed
WO-1999032488-A1 METHOD FOR PREPARING A HYDANTOIN DERIVATIVE SUBSTITUTED IN POSITION 5, METHOD FOR PREPARING AN α-AMINO ACID ALKALINE SALT FROM SAID HYDANTOIN DERIVATIVE AND METHOD FOR ESTERIFYING CYCLIC α-AMINO ACIDS SERANALIS (FR) 1999-07-01 — — WO disclosed
US-5723483-A NEUROTENSIN ANTAGONIST, HYPOTENSIVE AGENTS AND FOR NEUROPSYCHIATRIC DISORDERS SANOFI (FR) 1998-03-03 — — US disclosed
US-5585497-A USEFUL IN TREATMENT OF NEUROPSYCHIATRIC DISORDERS, ESPECIALLY THOSE ASSOCIATED WITH A DYSFUNCTION OF THE DOPAMINERGIC SYSTEMS SANOFI (FR) 1996-12-17 — — US disclosed
US-5523455-A PREPARED USING A NAPHTHYLHYDRAZINE CHEMICAL INTERMEDIATE SANOFI (FR) 1996-06-04 — — US disclosed
US-5502059-A DOPAMINERGIC DYSFUNCTION DISORDERS SANOFI (FR) 1996-03-26 — — US 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-20230257379-A1 INDOLIZINE DERIVATIVES AND THEIR APPLICATION IN MEDICINE INMT, IDO1, IDO2 GRM4 1294/4885CYP1A2 72/4885CYP2C19 40/4885
US-11970495-B2 Indolizine derivatives and their application in medicine INMT, IDO1, IDO2 GRM4 1294/4885CYP1A2 72/4885CYP2C19 40/4885
US-20230242527-A1 INDOLIZINE DERIVATIVES AND THEIR APPLICATION IN MEDICINE INMT, IDO1, IDO2 GRM4 1294/4885CYP1A2 72/4885CYP2C19 40/4885
US-11945817-B2 Indolizine derivatives and their application in medicine INMT, IDO1, IDO2 GRM4 1294/4885CYP1A2 72/4885CYP2C19 40/4885
US-20210253570-A1 INDOLIZINE DERIVATIVES AND THEIR APPLICATION IN MEDICINE INMT, IDO1, IDO2 GRM4 1294/4885CYP1A2 72/4885CYP2C19 40/4885
US-11655249-B2 Indolizine derivatives and their application in medicine INMT, IDO1, IDO2 GRM4 1294/4885CYP1A2 72/4885CYP2C19 40/4885

“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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