SCHEMBL7014148

SCHEMBL7014148

CNC1(C#N)CCN(C(=O)OC(C)(C)C)CC1

nearest known ligand 0.45

Predicted protein targets (top 16)

geneUniProtsupporting neighboursconfidence
USP2 O75604 1/20 0.45
SMN1; SMN2 Q16637 1/20 0.45
EPHX2 P34913 1/20 0.42
CTSK P43235 1/20 0.41
JAK2 O60674 3/20 0.41
JAK1 P23458 3/20 0.41
EPHX1 P07099 1/20 0.40
GPR119 Q8TDV5 1/20 0.40
MEN1 O00255 1/20 0.39
ALDH1A1 P00352 1/20 0.39
MAPT P10636 1/20 0.39
KMT2A Q03164 1/20 0.39
HPGD P15428 1/20 0.39
TSHR P16473 2/20 0.39
ALOX15 P16050 1/20 0.39
ATM Q13315 1/20 0.39

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
SCHEMBL1973674 0.83 USP2 (0.49) USP2SMN1; SMN2EPHX2CTSKEPHX1
SCHEMBL1684776 0.82 CTSS (0.43) USP2SMN1; SMN2EPHX2CTSKJAK2
SCHEMBL5751932 0.81 USP2 (0.44) USP2SMN1; SMN2EPHX2CTSKJAK2
SCHEMBL15461484 0.80 CTSK (0.40) USP2SMN1; SMN2EPHX2CTSKJAK2
SCHEMBL19625230 0.80 EPHX2 (0.39) USP2SMN1; SMN2EPHX2CTSKJAK2
SCHEMBL388054 0.80 USP2 (0.46) USP2SMN1; SMN2EPHX2CTSKJAK2
SCHEMBL22576321 0.80 KDM4E (0.45) USP2SMN1; SMN2EPHX2CTSKJAK2
SCHEMBL18319117 0.80 CTSL (0.43) USP2SMN1; SMN2EPHX2CTSKJAK2
SCHEMBL2887782 0.80 USP2 (0.49) USP2SMN1; SMN2EPHX2CTSKJAK2
SCHEMBL1118226 0.80 USP2 (0.49) USP2SMN1; SMN2EPHX2CTSKEPHX1

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 11 patents. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12624053-B2 Ras inhibitors Revolution Medicines, Inc. (US) 2026-05-12 US disclosed
US-20260070930-A1 RAS INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION, AS ADMINISTRATIVE AGENT 2026-03-12 US disclosed
US-20250388608-A1 RAS INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION, AS AGENT 2025-12-25 US disclosed
US-20250145643-A1 RAS INHIBITORS WILMINGTON TRUST, NATIONAL ASSOCIATION, AS AGENT 2025-05-08 US disclosed
CN-119798279-A RAS inhibitors 锐新医药公司 2025-04-11 CN disclosed
CN-118922423-A RAS inhibitors 锐新医药公司 2024-11-08 CN disclosed
CN-118561952-A RAS inhibitors 锐新医药公司 2024-08-30 CN disclosed
CN-118234731-A RAS inhibitors 锐新医药公司 2024-06-21 CN disclosed
EP-2433940-B9 SPIROIMIDAZOLONE DERIVATIVE CHUGAI PHARMACEUTICAL CO LTD (JP) 2015-10-28 EP disclosed
US-20030187023-A1 Sulfone derivatives, process for their production and use thereof TAKEDA PHARMACEUTICAL COMPANY LIMITED (JP) 2003-10-02 US disclosed
EP-1302462-A1 SULFONE DERIVATIVES, PROCESS FOR THEIR PRODUCTION AND USE THEREOF Takeda Chemical Industries, Ltd. (JP) 2003-04-16 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 (5 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-20260070930-A1 RAS INHIBITORS KRAS, NRAS, RIN1 USP2 2484/4885SMN1; SMN2 4241/4885EPHX2 1934/4885
US-20250145643-A1 RAS INHIBITORS KRAS, NRAS, HRAS USP2 1149/4885SMN1; SMN2 3728/4885EPHX2 3033/4885
US-12624053-B2 Ras inhibitors KRAS, NRAS, HMGCR USP2 2102/4885SMN1; SMN2 4495/4885EPHX2 2202/4885
US-20030187023-A1 Sulfone derivatives, process for their production and use thereof SULT1E1, RRS1, SHH USP2 3336/4885SMN1; SMN2 3830/4885EPHX2 2528/4885
US-20250388608-A1 RAS INHIBITORS KRAS, NRAS, HMGCR USP2 2102/4885SMN1; SMN2 4495/4885EPHX2 2202/4885

“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.