Mk-0893

Mk-0893

SCHEMBL29363684

COc1ccc2cc(-c3cc(-c4cc(Cl)cc(Cl)c4)nn3[C@@H](C)c3ccc(C(=O)NCCC(=O)O)cc3)ccc2c1

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

GCGR

The experimentally established mechanism targets of Mk-0893. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 12)

geneUniProtsupporting neighboursconfidence
▸ GCGR known ✓ P47871 20/20 1.00
▸ GIPR P48546 13/20 1.00
▸ VIPR2 P41587 4/20 1.00
▸ CYP1A2 P05177 1/20 1.00
▸ CYP3A4 P08684 1/20 1.00
▸ CYP2C8 P10632 1/20 1.00
▸ CYP2C9 P11712 1/20 1.00
▸ CYP2B6 P20813 1/20 1.00
▸ VIPR1 P32241 1/20 1.00
▸ DUSP2 Q05923 1/20 1.00
▸ GLP1R P43220 2/20 0.86
▸ KCNH2 Q12809 1/20 0.81

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
Mk-0893 SCHEMBL2355321 1.00 GCGR (1.00) GCGRGIPRVIPR2CYP1A2CYP3A4
Mk-0893 SCHEMBL675777 1.00 GCGR (1.00) GCGRGIPRVIPR2CYP1A2CYP3A4
SCHEMBL13644751 0.94 GCGR (0.88) GCGRGIPRVIPR2CYP1A2CYP3A4
SCHEMBL2667874 0.92 GCGR (0.84) GCGRGIPRVIPR2CYP1A2CYP3A4
SCHEMBL2667510 0.92 GCGR (0.84) GCGRGIPRVIPR2CYP1A2CYP3A4
SCHEMBL2667512 0.91 GCGR (0.83) GCGRGIPRVIPR2CYP1A2CYP3A4
SCHEMBL3251729 0.91 GCGR (0.83) GCGRGIPRVIPR2CYP1A2CYP3A4
SCHEMBL825813 0.91 GCGR (1.00) GCGRGIPRVIPR2CYP1A2CYP3A4
SCHEMBL1966239 0.91 GCGR (1.00) GCGRGIPRVIPR2CYP1A2CYP3A4
SCHEMBL827984 0.91 GCGR (1.00) GCGRGIPRVIPR2CYP1A2CYP3A4

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-114504573-A Application of MK-0893 in preparing products for inhibiting coronavirus and medicines for resisting coronavirus infection 山东大学 2022-05-17 — — CN claimed
US-12624116-B2 Methods of treating severe insulin resistance by interfering with glucagon receptor signaling REGENERON PHARMACEUTICALS, INC. (US) 2026-05-12 — — US disclosed
EP-4735449-A1 TETRACYCLIC COMPOUNDS CONTAINING A FUSED INDOLE FOR TREATING APOL1-MEDIATED CHRONIC KIDNEY DISEASE OmniAB, Inc. (US) 2026-05-06 — — EP disclosed
EP-4727552-A2 PASSIVE PERMEABLE PCSK9 ANTAGONIST COMPOUNDS Merck Sharp & Dohme LLC (US) 2026-04-22 — — EP disclosed
US-12577259-B2 PCSK9 antagonist compounds MERCK SHARP & DOHME LLC (US) 2026-03-17 — — US disclosed
EP-4705296-A1 HETEROARYLINDOLE INHIBITORS OF APOL-1 OmniAB, Inc. (US) 2026-03-11 — — EP disclosed
US-12540132-B2 Preparation of tetrahydroindazole derivatives as novel diacylglyceride O-acyltransferase 2 inhibitors MERCK SHARP & DOHME LLC (US) 2026-02-03 — — US disclosed
US-20260022125-A1 PYRROLOPYRIDAZINE VEGFR INHIBITORS MERCK SHARP & DOHME LLC (US) 2026-01-22 — — US disclosed
EP-4225739-B1 PREPARATION OF BENZIMIDAZOLONE DERIVATIVES AS NOVEL DIACYLGLYCERIDE O-ACYLTRANSFERASE 2 INHIBITORS MERCK SHARP & DOHME LLC (US) 2026-01-21 — — EP disclosed
EP-3954436-B1 METHOD FOR PRODUCING BIOTISSUE-LIKE STRUCTURE ORIZURU THERAPEUTICS INC (JP) 2026-01-07 — — EP disclosed
US-11319376-B2 Combination of glucagon receptor antagonists and PI3K pathway inhibitors for the treatment of cancer REMD BIOTHERAPEUTICS, INC. (US) 2022-05-03 — — US disclosed
US-11306125-B2 PCSK9 antagonists bicyclo-compounds MERCK SHARP & DOHME CORP. (US) 2022-04-19 — — US disclosed
US-20220112182-A1 PREPARATION OF BENZIMIDAZOLONE DERIVATIVES AS NOVEL DIACYLGLYCERIDE O-ACYLTRANSFERASE 2 INHIBITORS MERCK SHARP & DOHME CORP. (US) 2022-04-14 — — US disclosed
US-20220112181-A1 PREPARATION OF OXINDOLE DERIVATIVES AS NOVEL DIACYLGLYCERIDE O-ACYLTRANSFERASE 2 INHIBITORS MERCK SHARP & DOHME CORP. (US) 2022-04-14 — — US disclosed
EP-3974413-A1 ANTIDIABETIC SUBSTITUTED HETEROARYL COMPOUNDS MERCK SHARP & DOHME CORP. (US) 2022-03-30 — — EP disclosed
CN-106573966-B Compositions and methods for treating metabolic abnormalities NGM生物制药有限公司 2022-03-01 — — CN disclosed
EP-3954436-A1 METHOD FOR PRODUCING BIOTISSUE-LIKE STRUCTURE Orizuru Therapeutics, Inc. (JP) 2022-02-16 — — EP disclosed
US-20220041684-A1 ENGINEERED PLATELETS FOR TARGETED DELIVERY OF A THERAPEUTIC AGENT JPV01 LTD. (GB) 2022-02-10 — — US disclosed
EP-3947434-A2 ENGINEERED PLATELETS FOR TARGETED DELIVERY OF A THERAPEUTIC AGENT JPV01 Ltd (GB) 2022-02-09 — — EP disclosed
CN-113993528-A Method for producing living body-like tissue structure 千纸鹤治疗公司 2022-01-28 — — CN 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-12624116-B2 Methods of treating severe insulin resistance by interfering with glucagon receptor signaling GCGR, INSR, INSRR GCGR 1/4885GIPR 6/4885VIPR2 78/4885
US-12540132-B2 Preparation of tetrahydroindazole derivatives as novel diacylglyceride O-acyltransferase 2 inhibitors DGAT2, DGAT1, ACAT2 GCGR 128/4885GIPR 501/4885VIPR2 3703/4885
US-11306125-B2 PCSK9 antagonists bicyclo-compounds PCSK9, PCSK7, PCSK6 GCGR 190/4885GIPR 181/4885VIPR2 2037/4885
US-20260022125-A1 PYRROLOPYRIDAZINE VEGFR INHIBITORS FLT1, KDR, FLT4 GCGR 407/4885GIPR 237/4885VIPR2 1355/4885
US-20220112182-A1 PREPARATION OF BENZIMIDAZOLONE DERIVATIVES AS NOVEL DIACYLGLYCERIDE O-ACYLTRANSFERASE 2 INHIBITORS DGAT2, DGAT1, ACAT2 GCGR 210/4885GIPR 665/4885VIPR2 3170/4885
US-12577259-B2 PCSK9 antagonist compounds PCSK9, LDLR, PCSK6 GCGR 112/4885GIPR 100/4885VIPR2 2960/4885
US-20220112181-A1 PREPARATION OF OXINDOLE DERIVATIVES AS NOVEL DIACYLGLYCERIDE O-ACYLTRANSFERASE 2 INHIBITORS DGAT2, DGAT1, MOGAT2 GCGR 338/4885GIPR 675/4885VIPR2 1923/4885

“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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