SCHEMBL1920162

SCHEMBL1920162

COC(=O)C(C)C(=O)C(C)C(=O)OC

nearest known ligand 0.48

Predicted protein targets (top 19)

geneUniProtsupporting neighboursconfidence
SMN1; SMN2 Q16637 2/20 0.48
CA14 Q9ULX7 3/20 0.44
CA12 O43570 2/20 0.41
ALDH1A1 P00352 2/20 0.37
KMT2A Q03164 1/20 0.36
CA1 P00915 1/20 0.34
CA2 P00918 1/20 0.34
CA7 P43166 1/20 0.32
CA9 Q16790 1/20 0.32
ESR1 P03372 1/20 0.32
ESR2 Q92731 1/20 0.32
ZDHHC7 Q9NXF8 1/20 0.32
KEAP1 Q14145 1/20 0.32
NFE2L2 Q16236 1/20 0.32
HCAR2 Q8TDS4 1/20 0.32
TSHR P16473 1/20 0.32
MMP2 P08253 1/20 0.31
MMP9 P14780 1/20 0.31
MMP13 P45452 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
SCHEMBL27485803 0.92 SMN1; SMN2 (0.42) SMN1; SMN2CA14CA12ALDH1A1KMT2A
SCHEMBL16160087 0.88 SMN1; SMN2 (0.44) SMN1; SMN2CA14CA12ALDH1A1KMT2A
SCHEMBL275280 0.87 SMN1; SMN2 (0.52) SMN1; SMN2CA14CA12ALDH1A1KMT2A
SCHEMBL26658220 0.84 SMN1; SMN2 (0.50) SMN1; SMN2CA14CA12ALDH1A1KMT2A
SCHEMBL10805452 0.84 SMN1; SMN2 (0.50) SMN1; SMN2CA14CA12ALDH1A1KMT2A
SCHEMBL5076701 0.84 SMN1; SMN2 (0.41) SMN1; SMN2CA14CA12ALDH1A1KMT2A
SCHEMBL4476955 0.84 SMN1; SMN2 (0.41) SMN1; SMN2CA14CA12ALDH1A1KMT2A
SCHEMBL7096981 0.84 SMN1; SMN2 (0.41) SMN1; SMN2CA14CA12ALDH1A1KMT2A
SCHEMBL31175938 0.82 SMN1; SMN2 (0.35) SMN1; SMN2CA14CA12ALDH1A1KMT2A
Ammonia Solution, Strong SCHEMBL8809999 0.81 SMN1; SMN2 (0.48) SMN1; SMN2CA14CA12ALDH1A1KMT2A

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20250074890-A1 CYANOPYRIDINE AND CYANOPYRIMIDINE BCL6 DEGRADERS DANA-FARBER CANCER INSTITUTE, INC. (US) 2025-03-06 US disclosed
EP-4380919-A1 CYANOPYRIDINE AND CYANOPYRIMIDINE BCL6 DEGRADERS Dana-Farber Cancer Institute, Inc. (US) 2024-06-12 EP disclosed
CN-117980290-A Cyanopyridine and cyanopyrimidine BCL6 degrading agents 达纳-法伯癌症研究所公司 2024-05-03 CN disclosed
WO-2023015164-A1 CYANOPYRIDINE AND CYANOPYRIMIDINE BCL6 DEGRADERS DANA-FARBER CANCER INSTITUTE, INC. (US) 2023-02-09 WO disclosed
US-10428049-B2 TRPA1 modulators ALGOMEDIX, INC. (US) 2019-10-01 US disclosed
US-20190016701-A1 TRPA1 MODULATORS ALGOMEDIX, INC. (US) 2019-01-17 US disclosed
US-9951046-B2 TRPA1 modulators ALGOMEDIX, INC. (US) 2018-04-24 US disclosed
US-9951046-B2 TRPA1 modulators ALGOMEDIX, INC. (US) 2018-04-24 US disclosed
US-20170001983-A1 TRPA1 MODULATORS ALGOMEDIX, INC. 2017-01-05 US disclosed
US-20170001983-A1 TRPA1 MODULATORS ALGOMEDIX, INC. 2017-01-05 US disclosed
EP-1716135-A1 PIPERIDINYLCARBONYL-PYRROLIDINES AND THEIR USE AS MELANOCORTIN AGONISTS Pfizer Limited (GB) 2006-11-02 EP disclosed
US-7115757-B2 Capable of inducing chemiluminescence; substrates for immunoassay; stability; low background for measurement to present high sensitivity TOSOH CORPORATION (JP) 2006-10-03 US disclosed
WO-2005077935-A1 PIPERIDINYLCARBONYL-PYRROLIDINES AND THEIR USE AS MELANOCORTIN AGONISTS PFIZER LIMITED (GB) 2005-08-25 WO disclosed
US-20050176772-A1 Pharmaceutically active compounds PFIZER INC 2005-08-11 US disclosed
US-20050153365-A1 1, 2-dioxetane derivatives and reagents employing them TOSOH CORPORATION (JP) 2005-07-14 US disclosed
US-6844453-B2 1,2-Dioxetane derivatives and reagents employing them TOSOH CORPORATION (JP) 2005-01-18 US disclosed
US-20040176611-A1 1, 2-Dioxetane derivatives and reagents employing them TOSOH CORPORATION (JP) 2004-09-09 US disclosed
US-6747160-B2 CAPABLE OF INDUCING CHEMILUMINESCENCE; SUBSTRATES FOR IMMUNOASSAY; STABLE; LOW BACKGROUND FOR MEASUREMENT TO PRESENT HIGH SENSITIVITY TOSOH CORPORATION (JP) 2004-06-08 US disclosed
US-20030207329-A1 1, 2-Dioxetane derivatives and reagents employing them TOSOH CORPORATION (JP) 2003-11-06 US disclosed
EP-1342724-A1 1,2-dioxetane derivates and reagents employing them Tosoh Corporation (JP) 2003-09-10 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 (8 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-10428049-B2 TRPA1 modulators TRPA1, TRPV1, TRPV2 SMN1; SMN2 859/4885CA14 4645/4885CA12 4514/4885
US-20170001983-A1 TRPA1 MODULATORS TRPA1, TRPV1, TRPV2 SMN1; SMN2 859/4885CA14 4645/4885CA12 4514/4885
US-20050153365-A1 1, 2-dioxetane derivatives and reagents employing them DAO, AKR1B10, OXSR1 SMN1; SMN2 4357/4885CA14 2271/4885CA12 3041/4885
US-20250074890-A1 CYANOPYRIDINE AND CYANOPYRIMIDINE BCL6 DEGRADERS BCL6, BCL6B, BCOR SMN1; SMN2 2805/4885CA14 3288/4885CA12 3050/4885
US-20050176772-A1 Pharmaceutically active compounds MC4R, MC3R, MC5R SMN1; SMN2 2155/4885CA14 3173/4885CA12 4038/4885
US-20190016701-A1 TRPA1 MODULATORS TRPA1, TRPV1, TRPV2 SMN1; SMN2 859/4885CA14 4645/4885CA12 4514/4885
US-20030207329-A1 1, 2-Dioxetane derivatives and reagents employing them SRD5A1, DAO, SRD5A2 SMN1; SMN2 4205/4885CA14 1880/4885CA12 3349/4885
US-20040176611-A1 1, 2-Dioxetane derivatives and reagents employing them SRD5A1, DAO, SRD5A2 SMN1; SMN2 4205/4885CA14 1880/4885CA12 3349/4885

“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.