SCHEMBL5585204

SCHEMBL5585204

COC(=O)N1CCc2ccccc21

nearest known ligand 0.67

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NOTUM Q6P988 2/20 0.67
RAB9A P51151 7/20 0.61
NPC1 O15118 5/20 0.61
L3MBTL1 Q9Y468 1/20 0.61
SMN1; SMN2 Q16637 6/20 0.61
NFKB1 P19838 3/20 0.61
NFKB2 Q00653 3/20 0.61
RELA Q04206 3/20 0.61
MAPT P10636 3/20 0.61
PKM P14618 2/20 0.61
MAOB P27338 1/20 0.61
ALDH1A1 P00352 4/20 0.60
TSHR P16473 2/20 0.60
HPGD P15428 2/20 0.58
TP53 P04637 2/20 0.58
USP2 O75604 1/20 0.57
KMT2A Q03164 2/20 0.57
MEN1 O00255 1/20 0.57
POLB P06746 1/20 0.56
SIGMAR1 Q99720 1/20 0.56

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
SCHEMBL30721522 1.00 NOTUM (0.67) NOTUMRAB9ANPC1L3MBTL1SMN1; SMN2
SCHEMBL30039812 0.90 NOTUM (0.69) NOTUML3MBTL1SMN1; SMN2MAPTALDH1A1
SCHEMBL926908 0.90 NOTUM (0.69) NOTUML3MBTL1SMN1; SMN2MAPTALDH1A1
SCHEMBL30401717 0.89 NOTUM (0.67) NOTUML3MBTL1SMN1; SMN2MAPTALDH1A1
SCHEMBL9530206 0.89 NOTUM (0.62) NOTUMSMN1; SMN2MAPTALDH1A1TSHR
SCHEMBL2116912 0.83 NPC1 (0.71) NOTUMRAB9ANPC1L3MBTL1SMN1; SMN2
SCHEMBL29554766 0.83 NPC1 (0.71) NOTUMRAB9ANPC1L3MBTL1SMN1; SMN2
SCHEMBL30681385 0.83 RAB9A (0.66) NOTUMRAB9ANPC1L3MBTL1SMN1; SMN2
SCHEMBL12282796 0.82 NOTUM (0.67) NOTUMRAB9ANPC1L3MBTL1SMN1; SMN2
SCHEMBL30900483 0.82 NOTUM (0.61) NOTUMRAB9ANPC1L3MBTL1SMN1; SMN2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-115894327-A Process for preparing indoline carboxylic ester 阿拉善盟锦源科技发展有限公司 2023-04-04 CN claimed
EP-3204347-B1 ENAMINE COMPOUNDS FOR PROTECTING AGAINST UV RADIATION COMMW SCIENT IND RES ORG (AU) 2024-10-23 EP disclosed
EP-3670515-B1 PYRIMIDO-DIAZEPINONE COMPOUNDS AND METHODS OF TREATING DISORDERS DANA FARBER CANCER INST INC (US) 2024-03-06 EP disclosed
CN-115894327-A Process for preparing indoline carboxylic ester 阿拉善盟锦源科技发展有限公司 2023-04-04 CN disclosed
CN-115894327-A Process for preparing indoline carboxylic ester 阿拉善盟锦源科技发展有限公司 2023-04-04 CN disclosed
US-11512042-B2 Enamine compounds for absorbance of electromagnetic energy COMMONWEALTH SCIENTIFIC AND INDUSTRIAL RESEARCH ORGANISATION (AU) 2022-11-29 US disclosed
CN-107108429-B Compound (I) 联邦科学与工业研究组织 2022-08-19 CN disclosed
US-11024812-B2 Compound for organic-electric element, organic-electric element using same, and electronic device for same DUK SAN NEOLUX CO., LTD. (KR) 2021-06-01 US disclosed
US-11024812-B2 Compound for organic-electric element, organic-electric element using same, and electronic device for same DUK SAN NEOLUX CO., LTD. (KR) 2021-06-01 US disclosed
EP-3738964-A1 PYRIMIDO-DIAZEPINONE COMPOUNDS AND METHODS OF TREATING DISORDERS Dana Farber Cancer Institute, Inc. (US) 2020-11-18 EP disclosed
US-20030166650-A1 Cinnamide derivatives as KCNQ potassium channel modulators BRISTOL-MYERS SQUIBB COMPANY 2003-09-04 US disclosed
CN-1374349-A Process for producing asymmetric hypomethyl dye BAYER AG (DE) 2002-10-16 CN disclosed
EP-0687251-B1 1,3-DIHYDROINDOL-2-ONE DERIVATIVES SUBSTITUTED IN POSITION 3 BY A NITROGEN GROUP AS VASOPRESSIN AND/OR OCYTOCINE AGONISTS AND/OR ANTAGONISTS SANOFI SYNTHELABO (FR) 2002-02-27 EP disclosed
US-5773612-A VASOPRESSIN OR OXYTOCIN RECEPTORS SANOFI (FR) 1998-06-30 US disclosed
US-5594023-A 1,3-dihydroindol-2-one derivatives substituted in the 3-position by a nitrogen-containing group, their preparation and the pharmaceutical compositions in which they are present SANOFI (FR) 1997-01-14 US disclosed
EP-0687251-A1 1,3-DIHYDROINDOL-2-ONE DERIVATIVES SUBSTITUTED IN POSITION 3 BY A NITROGEN GROUP AS VASOPRESSIN AND/OR OCYTOCINE AGONISTS AND/OR ANTAGONISTS SANOFI (FR) 1995-12-20 EP disclosed
WO-1995018105-A1 1,3-DIHYDROINDOL-2-ONE DERIVATIVES SUBSTITUTED IN POSITION 3 BY A NITROGEN GROUP AS VASOPRESSIN AND/OR OCYTOCINE AGONISTS AND/OR ANTAGONISTS SANOFI (FR) 1995-07-06 WO disclosed
US-5401738-A Angiotensin antagonist, hypotensive, aldosteronism, cardiac insufficiency MERCK PATENT GESELLSCHAFT MIT BESCHRANKTER (DE) 1995-03-28 US disclosed
CN-1082542-A Benzimidizole derivatives MERCK PATENT GMBH (DE) 1994-02-23 CN disclosed
EP-0574787-A2 Benzimidazole derivatives as angiotensin II antagonists MERCK PATENT GmbH (DE) 1993-12-22 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-11024812-B2 Compound for organic-electric element, organic-electric element using same, and electronic device for same PIEZO1, OR10J3, OR51E2 NOTUM 73/4885RAB9A 3738/4885NPC1 3510/4885
US-20030166650-A1 Cinnamide derivatives as KCNQ potassium channel modulators KCNH2, KCNH3, KCNQ1 NOTUM 2404/4885RAB9A 1857/4885NPC1 189/4885
US-11512042-B2 Enamine compounds for absorbance of electromagnetic energy ENO1, NQO1, NNMT NOTUM 4567/4885RAB9A 2329/4885NPC1 4139/4885

“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.