SCHEMBL59435

SCHEMBL59435

CC(C)[C@@H](C(=O)O)N(C)C(=O)OC(C)(C)C

nearest known ligand 0.33

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
CA1 P00915 1/20 0.33
CA2 P00918 1/20 0.33
CA7 P43166 1/20 0.33
AAK1 Q2M2I8 2/20 0.32
MMP13 P45452 1/20 0.32
MEN1 O00255 1/20 0.32
GAA P10253 1/20 0.32
KMT2A Q03164 1/20 0.32
CTSS P25774 1/20 0.31
CTSK P43235 1/20 0.31
ADAMTS4 O75173 1/20 0.31
HDAC1 Q13547 1/20 0.31
HDAC2 Q92769 1/20 0.31
HDAC6 Q9UBN7 1/20 0.31

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
SCHEMBL67120 1.00 CA1 (0.33) CA1CA2CA7AAK1MMP13
SCHEMBL2160514 1.00 CA1 (0.33) CA1CA2CA7AAK1MMP13
SCHEMBL28058555 0.98 CA1 (0.32) CA1CA2CA7AAK1MMP13
SCHEMBL26449280 0.89 MMP13 (0.31) CA1CA2CA7AAK1MMP13
SCHEMBL26449237 0.89 MMP13 (0.31) CA1CA2CA7AAK1MMP13
SCHEMBL23749797 0.87 HDAC6 (0.32) CA1CA2CA7AAK1MMP13
SCHEMBL26449279 0.87 HDAC6 (0.32) CA1CA2CA7AAK1MMP13
SCHEMBL26449223 0.87 HDAC6 (0.32) CA1CA2CA7AAK1MMP13
SCHEMBL6843570 0.87 AAK1 (0.32) AAK1MMP13MEN1GAAKMT2A
SCHEMBL1486172 0.87 AAK1 (0.32) AAK1MMP13MEN1GAAKMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9458127-B2 Bis-acylated hydroxylamine derivatives CARDIOXYL PHARMACEUTICALS, INC. (US) 2016-10-04 US claimed
US-20150197502-A1 Bis-Acylated Hydroxylamine Derivatives THE JOHNS HOPKINS UNIVERSITY 2015-07-16 US claimed
US-20260132119-A1 Alkylphenyl Substituted Compounds, Compositions and Methods of Use DEEP APPLE THERAPEUTICS, INC. (US) 2026-05-14 US disclosed
US-12622944-B2 Compositions containing, methods involving, and uses of non-natural amino acid linked dolastatin derivatives AMBRX, INC. (US) 2026-05-12 US disclosed
WO-2026090116-A2 RAS INHIBITORS Revolution Medicines, Inc. (US) 2026-04-30 WO disclosed
EP-4558507-B1 MACROCYCLE COMPOUNDS FOR THE TREATMENT OF CANCER HOFFMANN LA ROCHE (CH) 2026-04-29 EP disclosed
US-20260108619-A1 CONJUGATION LINKERS, CELL BINDING MOLECULE-DRUG CONJUGATES CONTAINING THE LINKERS, METHODS OF MAKING AND USES SUCH CONJUGATES WITH THE LINKERS HANGZHOU DAC BIOTECH CO., LTD. (CN) 2026-04-23 US disclosed
US-20260091081-A1 A FORMULATION OF A CONJUGATE OF A TUBULYSIN ANALOG TO A CELL-BINDING MOLECULE HANGZHOU DAC BIOTECH CO., LTD (CN) 2026-04-02 US disclosed
US-12576124-B2 Formulation of a conjugate of a tubulysin analog to a cell-binding molecule HANGZHOU DAC BIOTECH CO., LTD (CN) 2026-03-17 US disclosed
WO-2026041636-A1 MACROCYCLE COMPOUNDS FOR THE TREATMENT OF CANCER F. HOFFMANN-LA ROCHE AG (CH) 2026-02-26 WO disclosed
EP-4696316-A2 RAS INHIBITORS Revolution Medicines, Inc. (US) 2026-02-18 EP disclosed
EP-0760822-A1 ANTI-FUNGAL CYCLIC DEPSIPEPTIDES SCHERING CORPORATION (US) 1997-03-12 EP disclosed
EP-0408973-B1 Antiherpes pentapeptides BIO MEGA BOEHRINGER INGELHEIM (CA) 1996-10-23 EP disclosed
US-5552384-A Antiherpes compositions and method of use BIO-MEGA BOEHRINGER INGELHEIM RESEARCH INC. (CA) 1996-09-03 US disclosed
US-5502036-A VIRICIDES BIOMEGA BOEHRINGER INGELHEIM RESEARCH INC. (CA) 1996-03-26 US disclosed
WO-1995030692-A1 ANTI-FUNGAL CYCLIC DEPSIPEPTIDES SCHERING CORPORATION (US) 1995-11-16 WO disclosed
EP-0411334-B1 Antiherpes pentapeptide derivatives having a substituted aspartic acid side chain BIO MEGA BOEHRINGER INGELHEIM (CA) 1995-02-22 EP disclosed
EP-0618221-A2 Heterocyclic inhibitors of farnesyl protein transferase BRISTOL-MYERS SQUIBB COMPANY (US) 1994-10-05 EP disclosed
EP-0493770-A2 Antiherpes compositions BIO-MEGA/BOEHRINGER INGELHEIM RESEARCH INC. (CA) 1992-07-08 EP disclosed
EP-0411334-A1 Antiherpes pentapeptide derivatives having a substituted aspartic acid side chain BIO-MEGA/BOEHRINGER INGELHEIM RESEARCH INC. (CA) 1991-02-06 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 (6 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-20150197502-A1 Bis-Acylated Hydroxylamine Derivatives CPT1A, TNNI3, NOS2 CA1 1379/4885CA2 627/4885CA7 895/4885
US-12576124-B2 Formulation of a conjugate of a tubulysin analog to a cell-binding molecule CD4, TAP1, MCTS1 CA1 317/4885CA2 354/4885CA7 1209/4885
US-12622944-B2 Compositions containing, methods involving, and uses of non-natural amino acid linked dolastatin derivatives DDOST, DMPK, KRTCAP2 CA1 2190/4885CA2 1027/4885CA7 744/4885
US-20260091081-A1 A FORMULATION OF A CONJUGATE OF A TUBULYSIN ANALOG TO A CELL-BINDING MOLECULE CD4, MALT1, LY6K CA1 336/4885CA2 492/4885CA7 173/4885
US-20260132119-A1 Alkylphenyl Substituted Compounds, Compositions and Methods of Use GIPR, MC2R, GRPR CA1 1996/4885CA2 403/4885CA7 162/4885
US-20260108619-A1 CONJUGATION LINKERS, CELL BINDING MOLECULE-DRUG CONJUGATES CONTAINING THE LINKERS, METHODS OF MAKING AND USES SUCH CONJUGATES WITH THE LINKERS DCLRE1A, CCR3, CCR8 CA1 409/4885CA2 1262/4885CA7 441/4885

“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.