SCHEMBL842922

SCHEMBL842922

CC(C)CN(O)C(=O)OC(C)(C)C

nearest known ligand 0.36

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
HDAC6 Q9UBN7 2/20 0.36
HDAC1 Q13547 1/20 0.36
HDAC2 Q92769 1/20 0.36
CA1 P00915 3/20 0.34
CA2 P00918 3/20 0.34
CA12 O43570 2/20 0.34
CA9 Q16790 1/20 0.34
CA7 P43166 1/20 0.34
CA14 Q9ULX7 2/20 0.33
NFKB1 P19838 1/20 0.33
NFKB2 Q00653 1/20 0.33
RELA Q04206 1/20 0.33
CTSL P07711 1/20 0.31
CTSB P07858 1/20 0.31
CTSS P25774 1/20 0.31
CTSK P43235 1/20 0.31
CYP2D6 P10635 1/20 0.31
AAK1 Q2M2I8 1/20 0.31
DGAT1 O75907 1/20 0.30
KCNA5 P22460 1/20 0.30

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
SCHEMBL23870601 0.82 HDAC6 (0.33) HDAC6HDAC1HDAC2CA1CA2
SCHEMBL20326558 0.81 CA1 (0.45) HDAC6HDAC1HDAC2CA1CA2
SCHEMBL13490197 0.79 HDAC6 (0.36) HDAC6HDAC1HDAC2CA1CA2
SCHEMBL854273 0.78 HDAC6 (0.35) HDAC6HDAC1HDAC2CA1CA2
SCHEMBL25123692 0.78 HDAC6 (0.35) HDAC6HDAC1HDAC2CA1CA2
SCHEMBL843324 0.78 HDAC6 (0.35) HDAC6HDAC1HDAC2CA1CA2
SCHEMBL19750797 0.76 CA1 (0.41) HDAC6HDAC1HDAC2CA1CA2
SCHEMBL3940725 0.76 HDAC6 (0.39) HDAC6HDAC1HDAC2CA1CA2
SCHEMBL21025722 0.75 ALDH1A1 (0.38) HDAC6HDAC1HDAC2CA1CA2
SCHEMBL20315020 0.75 CA14 (0.40) HDAC6HDAC1HDAC2CA1CA2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-4683669-A2 COMBINATIONS AND METHODS FOR ENHANCING CHECKPOINT INHIBITOR THERAPIES IN CANCER TREATMENT Purdue Research Foundation (US) 2026-01-28 EP disclosed
US-20250352652-A1 COMPOUNDS AND METHODS FOR THE TREATMENT AND PREVENTION OF FIBROTIC DISEASE STATES AND CANCER PURDUE RESEARCH FOUNDATION 2025-11-20 US disclosed
US-20250269036-A1 METHODS FOR ENHANCEMENT OF ENGINEERED CELL THERAPIES IN CANCER TREATMENT PURDUE RESEARCH FOUNDATION 2025-08-28 US disclosed
US-12397059-B2 Compounds and methods for the treatment and prevention of fibrotic disease states and cancer PURDUE RESEARCH FOUNDATION (US) 2025-08-26 US disclosed
WO-2024197318-A2 COMBINATIONS AND METHODS FOR ENHANCING CHECKPOINT INHIBITOR THERAPIES IN CANCER TREATMENT PURDUE RESEARCH FOUNDATION (US) 2024-09-26 WO disclosed
CN-117858706-A Methods of enhancing engineered cell therapies in cancer treatment 普渡研究基金会 2024-04-09 CN disclosed
EP-4271378-A1 METHODS FOR ENHANCEMENT OF ENGINEERED CELL THERAPIES IN CANCER TREATMENT Purdue Research Foundation (US) 2023-11-08 EP disclosed
EP-3898630-B1 NOVEL IMIDAZOPYRAZINE DERIVATIVES HOFFMANN LA ROCHE (CH) 2023-05-10 EP disclosed
US-20230022724-A1 NOVEL IMIDAZOPYRAZINE DERIVATIVES HOFFMANN-LA ROCHE INC. (US) 2023-01-26 US disclosed
US-20230013602-A1 NOVEL IMIDAZOPYRAZINE DERIVATIVES HOFFMANN-LA ROCHE INC. (US) 2023-01-19 US disclosed
US-20030055261-A1 Compounds with growth hormone releasing properties HELSINN THERAPEUTICS (U.S.), INC. 2003-03-20 US disclosed
US-20030040483-A1 Compounds with growth hormone releasing properties HELSINN THERAPEUTICS (U.S.), INC. 2003-02-27 US disclosed
EP-0777471-B1 INHIBITION OF LEUKOTRIENE BIOSYNTHESIS WITH UREA DERIVATIVES MINNESOTA MINING & MFG (US) 2002-11-27 EP disclosed
US-6127391-A A PEPTIDE MIMETIC COMPOUND FOR STIMULATING THE RELEASE OF GROWTH HORMONE FROM THE PITUITARY NOVO NORDISK A/S (DK) 2000-10-03 US disclosed
US-5977178-A Compounds with growth hormone releasing properties NOVO NORDISK A/S (DK) 1999-11-02 US disclosed
EP-0869974-A1 COMPOUNDS WITH GROWTH HORMONE RELEASING PROPERTIES NOVO NORDISK A/S (DK) 1998-10-14 EP disclosed
WO-1997023508-A1 COMPOUNDS WITH GROWTH HORMONE RELEASING PROPERTIES NOVO NORDISK A/S (DK) 1997-07-03 WO disclosed
EP-0777471-A1 INHIBITION OF LEUKOTRIENE BIOSYNTHESIS WITH UREA DERIVATIVES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-06-11 EP disclosed
US-5612377-A OXYUREA DERIVATIVE MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1997-03-18 US disclosed
WO-1996003983-A1 INHIBITION OF LEUKOTRIENE BIOSYNTHESIS WITH UREA DERIVATIVES MINNESOTA MINING AND MANUFACTURING COMPANY (US) 1996-02-15 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 (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-20230022724-A1 NOVEL IMIDAZOPYRAZINE DERIVATIVES MRPL21, O60361, MYD88 HDAC6 518/4885HDAC1 158/4885HDAC2 666/4885
US-20030055261-A1 Compounds with growth hormone releasing properties GHRHR, GHSR, IGFBP1 HDAC6 3764/4885HDAC1 1830/4885HDAC2 3809/4885
US-12397059-B2 Compounds and methods for the treatment and prevention of fibrotic disease states and cancer MSR1, MIF, MMP12 HDAC6 413/4885HDAC1 243/4885HDAC2 526/4885
US-20250269036-A1 METHODS FOR ENHANCEMENT OF ENGINEERED CELL THERAPIES IN CANCER TREATMENT CD47, FOLR1, CD14 HDAC6 1103/4885HDAC1 645/4885HDAC2 1006/4885
US-20230013602-A1 NOVEL IMIDAZOPYRAZINE DERIVATIVES IL4, RPS4Y1, RPS4X HDAC6 445/4885HDAC1 392/4885HDAC2 647/4885
US-20030040483-A1 Compounds with growth hormone releasing properties GHRHR, GHSR, GRPR HDAC6 3658/4885HDAC1 1467/4885HDAC2 3372/4885
US-20250352652-A1 COMPOUNDS AND METHODS FOR THE TREATMENT AND PREVENTION OF FIBROTIC DISEASE STATES AND CANCER MSR1, MIF, MMP12 HDAC6 413/4885HDAC1 243/4885HDAC2 526/4885

“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.