SCHEMBL2837530

SCHEMBL2837530

COC(=O)C(N)CNC(=O)OC(C)(C)C

nearest known ligand 0.44

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
MEN1 O00255 1/20 0.44
GAA P10253 1/20 0.44
KMT2A Q03164 1/20 0.44
TDP1 Q9NUW8 1/20 0.42
CA12 O43570 4/20 0.41
CA14 Q9ULX7 2/20 0.41
SYK P43405 1/20 0.41
SERPINE1 P05121 1/20 0.41
MAOA P21397 1/20 0.41
MAOB P27338 1/20 0.41
CA2 P00918 4/20 0.39
CA1 P00915 3/20 0.39
CA9 Q16790 2/20 0.39
CASR P41180 1/20 0.38
CA7 P43166 1/20 0.38
CTSL P07711 1/20 0.37
CTSB P07858 1/20 0.37
CTSS P25774 1/20 0.37
CTSK P43235 1/20 0.37
AAK1 Q2M2I8 1/20 0.36

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
SCHEMBL1854219 1.00 MEN1 (0.44) MEN1GAAKMT2ATDP1CA12
SCHEMBL584353 1.00 MEN1 (0.44) MEN1GAAKMT2ATDP1CA12
Hydrochloric Acid SCHEMBL584352 0.98 MEN1 (0.42) MEN1GAAKMT2ATDP1CA12
Hydrochloric Acid SCHEMBL2681080 0.98 MEN1 (0.42) MEN1GAAKMT2ATDP1CA12
Hydrochloric Acid SCHEMBL584354 0.98 MEN1 (0.42) MEN1GAAKMT2ATDP1CA12
Hydrochloric Acid SCHEMBL23575089 0.98 MEN1 (0.42) MEN1GAAKMT2ATDP1CA12
SCHEMBL27711551 0.91 MEN1 (0.45) MEN1GAAKMT2ATDP1CA12
Hydrochloric Acid SCHEMBL3894157 0.89 MEN1 (0.44) MEN1GAAKMT2ATDP1CA12
SCHEMBL20999543 0.89 MAOA (0.39) MEN1GAAKMT2ATDP1CA12
SCHEMBL23455567 0.89 MAOA (0.39) MEN1GAAKMT2ATDP1CA12

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-118307534-A LTA4H inhibitors and uses thereof 上海海雁医药科技有限公司 2024-07-09 CN disclosed
US-20230226207-A1 Camptothecin Drug Having High-Stability Hydrophilic Connecting Unit And Conjugate Thereof SYSTIMMUNE, INC. 2023-07-20 US disclosed
CN-115942872-A Method for inducing environmental stress tolerance in plants 味之素株式会社 2023-04-07 CN disclosed
CN-115916784-A Novel imidazopyrazine derivatives 豪夫迈·罗氏有限公司 2023-04-04 CN disclosed
CN-114380887-A Liquid phase fragment synthesis method of snake venom-like tripeptide 深圳翰宇药业股份有限公司 2022-04-22 CN disclosed
WO-2021136808-A1 CONJUGATES UNDERGOING INTRAMOLECULAR REARRANGEMENTS ASCENDIS PHARMA A/S (DK) 2021-07-08 WO disclosed
US-9676785-B2 HCV protease inhibitors and uses thereof CELGENE CAR LLC (BM) 2017-06-13 US disclosed
US-9676785-B2 HCV protease inhibitors and uses thereof CELGENE CAR LLC (BM) 2017-06-13 US disclosed
US-9663488-B2 Metalloenzyme inhibitor compounds VIAMET PHARMACEUTICALS, INC. (US) 2017-05-30 US disclosed
US-9663488-B2 Metalloenzyme inhibitor compounds VIAMET PHARMACEUTICALS, INC. (US) 2017-05-30 US disclosed
US-6274620-B1 2-BENZENESULFONYLAMINO-3-((5-BROMO-THIOPHENE-2-CARBONYL)-AMINO )PROPIONIC ACID-TERT-BUTYL ESTERS AS ANGIOGENESIS INHIBITORS; ANTICARCINOGENIC AGENTS; OSTEOPOROSIS, RESTENOSIS, AND OCULAR NEOVASCULARIZATION BIOCHEM PHARMA INC. (CA) 2001-08-14 US disclosed
EP-1115724-A1 QUINOLIZINONES AS INTEGRIN INHIBITORS Shire Biochem Inc. (CA) 2001-07-18 EP disclosed
WO-2000075129-A1 THIOPHENE INTEGRIN INHIBITORS SHIRE BIOCHEM INC. (CA) 2000-12-14 WO disclosed
WO-2000017197-A1 QUINOLIZINONES AS INTEGRIN INHIBITORS BIOCHEM PHARMA INC. (US) 2000-03-30 WO disclosed
US-5972984-A LOW MOLECULAR WEIGHT PEPTIDYL COMPOUNDS THAT DO NOT HAVE A THIOL MOIETY. MERCK & CO., INC. (US) 1999-10-26 US disclosed
EP-0833633-A4 INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE MERCK & CO INC (US) 1999-03-24 EP disclosed
US-5760028-A TREATING CANCER METASTASIS, DIABETIC RETINOPATHY, NEOVASCULAR GLAUCOMA, THROMBOSIS, RESTENOSIS, OSTEOPOROSIS, MACULAR DEGENERATION THE DUPONT MERCK PHARMACEUTICAL COMPANY (US) 1998-06-02 US disclosed
US-5756528-A ANTICARCINOGENIC AGENTS MERCK & CO., INC. (US) 1998-05-26 US disclosed
EP-0833633-A1 INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE Merck & Co., Inc. (US) 1998-04-08 EP disclosed
WO-1996039137-A1 INHIBITORS OF FARNESYL-PROTEIN TRANSFERASE MERCK & CO., INC. (US) 1996-12-12 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 (1 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-20230226207-A1 Camptothecin Drug Having High-Stability Hydrophilic Connecting Unit And Conjugate Thereof SLC7A1, CD44, DCLRE1A MEN1 753/4885GAA 3473/4885KMT2A 3696/4885

“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.