SCHEMBL29361023

SCHEMBL29361023

CC[C@H](C)[C@H](NC(=O)[C@H](CCC(=O)O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@@H](N)CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N[C@@H](CCCN=C(N)N)C(=O)N1CCC[C@H]1C(=O)N[C@@H](CO)C(=O)N[C@@H](Cc1ccc(O)cc1)C(=O)N[C@@H](CCCN=C(N)N)C(=O)O

nearest known ligand 0.74

Predicted protein targets (top 6)

geneUniProtsupporting neighboursconfidence
▸ NTSR1 P30989 12/20 0.74
▸ NTSR2 O95665 7/20 0.74
▸ SORT1 Q99523 4/20 0.74
▸ OPRD1 P41143 3/20 0.71
▸ OPRM1 P35372 1/20 0.71
▸ OPRK1 P41145 1/20 0.71

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
SCHEMBL30472155 0.90 NTSR1 (0.87) NTSR1NTSR2SORT1
SCHEMBL29416842 0.90 NTSR1 (0.87) NTSR1NTSR2SORT1
SCHEMBL29398203 0.90 NTSR1 (0.87) NTSR1NTSR2SORT1
SCHEMBL31280899 0.89 NTSR1 (0.74) NTSR1NTSR2SORT1OPRD1OPRM1
SCHEMBL29357887 0.89 OPRD1 (0.63) NTSR1NTSR2SORT1OPRD1OPRM1
SCHEMBL29353193 0.89 OPRD1 (0.63) NTSR1NTSR2SORT1OPRD1OPRM1
SCHEMBL30880437 0.88 NTSR1 (0.82) NTSR1NTSR2SORT1
SCHEMBL30999858 0.87 NTSR1 (0.62) NTSR1NTSR2SORT1OPRD1OPRM1
SCHEMBL30431861 0.87 NTSR1 (0.61) NTSR1NTSR2SORT1
SCHEMBL29725007 0.87 NTSR2 (0.71) NTSR1NTSR2SORT1OPRD1OPRM1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12583825-B2 Benzo[h]quinazolin-4-amine and thieno[3,2-h]quinazolin-4-amine derivatives for the treatment of cancer Redona Therapeutics, Inc. (US) 2026-03-24 — — US disclosed
EP-4698529-A1 BLOOD BRAIN BARRIER PENETRATING SELECTIVE INHIBITORS OF ROCK2 PROTEIN KINASES AND USES THEREOF Genosco Inc. (US) 2026-02-25 — — EP disclosed
EP-4698528-A1 SELECTIVE INHIBITORS OF ROCK2 PROTEIN KINASES AND USES THEREOF Genosco Inc. (US) 2026-02-25 — — EP disclosed
US-20250388567-A1 SELECTIVE G PROTEIN-COUPLED RECEPTOR KINASE 5 INHIBITORS, COMPOSITIONS, AND METHODS OF USE PURDUE RESEARCH FOUNDATION (US) 2025-12-25 — — US disclosed
US-20250346587-A1 NITROGEN-CONTAINING FIVE-MEMBERED HETEROCYCLIC DERIVATIVES AS CHECKPOINT KINASE 1 INHIBITOR AND USES THEREOF SPEROGENIX THERAPEUTICS LTD (CN) 2025-11-13 — — US disclosed
US-12435059-B2 AMP-activated protein kinase inhibitors and methods of making and using the same THE REGENTS OF THE UNIVERSITY OF COLORADO, A BODY CORPORATE (US) 2025-10-07 — — US disclosed
EP-4554944-A2 KINASE INHIBITORS The United States of America, as represented by the Secretary, Department of Health and Human Services (US) 2025-05-21 — — EP disclosed
WO-2025097025-A1 PROTEIN KINASE C (PKC) THETA INHIBITOR COMPOUNDS EVOMMUNE, INC. (US) 2025-05-08 — — WO disclosed
CN-113227054-B ROCK kinase inhibitors 切尔韦洛治疗有限责任公司 2025-04-11 — — CN disclosed
EP-4532492-A1 NITROGEN-CONTAINING FIVE-MEMBERED HETEROCYCLIC DERIVATIVES AS CHECKPOINT KINASE 1 INHIBITOR AND USES THEREOF Sperogenix Therapeutics Limited (HK) 2025-04-09 — — EP disclosed
WO-2022150381-A1 SELECTIVE INHIBITORS OF ROCK1 AND ROCK2 PROTEIN KINASES AND USES THEREOF Genosco Inc. (US) 2022-07-14 — — WO disclosed
CN-114380798-A Salts of Pim kinase inhibitors 因赛特公司 2022-04-22 — — CN disclosed
US-20220119406-A1 SUBSTITUTED ISOQUINOLINES AS ROCK KINASE INHIBITORS Cervello Therapeutics LLC (US) 2022-04-21 — — US disclosed
WO-2022074143-A1 BENZO[H]QUINAZOLIN-4-AMINE AND THIENO[3,2-H]QUINAZOLIN-4-AMINE DERIVATIVES FOR THE TREATMENT OF CANCER Basilea Pharmaceutica International AG (CH) 2022-04-14 — — WO disclosed
EP-3347351-B1 SALTS OF A PIM KINASE INHIBITOR INCYTE CORP (US) 2022-03-30 — — EP disclosed
US-11278541-B2 Low dose combination therapy for treatment of myeloproliferative neoplasms INCYTE CORPORATION (US) 2022-03-22 — — US disclosed
CN-114222747-A PIM kinase inhibitor composition and application thereof 斯奈普生物公司 2022-03-22 — — CN disclosed
EP-3962916-A1 PIM KINASE INHIBITOR COMPOSITIONS AND USES THEREOF Snap Bio, Inc. (US) 2022-03-09 — — EP disclosed
CN-108715590-B Thiazolecarboxamide and picolinamide compounds useful as PIM kinase inhibitors 因赛特公司 2022-03-08 — — CN disclosed
US-11229631-B2 Thiazolecarboxamides and pyridinecarboxamide compounds useful as Pim kinase inhibitors INCYTE CORPORATION (US) 2022-01-25 — — 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 (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-20250388567-A1 SELECTIVE G PROTEIN-COUPLED RECEPTOR KINASE 5 INHIBITORS, COMPOSITIONS, AND METHODS OF USE GRK5, GRK3, GRK2 NTSR1 952/4885NTSR2 1141/4885SORT1 4420/4885
US-20250346587-A1 NITROGEN-CONTAINING FIVE-MEMBERED HETEROCYCLIC DERIVATIVES AS CHECKPOINT KINASE 1 INHIBITOR AND USES THEREOF CHEK1, CHEK2, BUB1 NTSR1 3382/4885NTSR2 3850/4885SORT1 4852/4885
US-11278541-B2 Low dose combination therapy for treatment of myeloproliferative neoplasms PIM1, JAK2, JAK1 NTSR1 2687/4885NTSR2 3301/4885SORT1 4442/4885
US-12435059-B2 AMP-activated protein kinase inhibitors and methods of making and using the same PRKAA1, PRKAA2, PRKAG1 NTSR1 3608/4885NTSR2 3179/4885SORT1 4365/4885
US-11229631-B2 Thiazolecarboxamides and pyridinecarboxamide compounds useful as Pim kinase inhibitors PIM2, PIM1, PIM3 NTSR1 3870/4885NTSR2 3323/4885SORT1 4826/4885
US-12583825-B2 Benzo[h]quinazolin-4-amine and thieno[3,2-h]quinazolin-4-amine derivatives for the treatment of cancer H1-3, RB1, H1-2 NTSR1 473/4885NTSR2 533/4885SORT1 4882/4885
US-20220119406-A1 SUBSTITUTED ISOQUINOLINES AS ROCK KINASE INHIBITORS ROCK1, ROCK2, CIT NTSR1 3765/4885NTSR2 3243/4885SORT1 4432/4885

“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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