SCHEMBL4188554

SCHEMBL4188554

CC(C)(C)[Si](C)(C)OCCOS(C)(=O)=O

nearest known ligand 0.44

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
USP2 O75604 2/20 0.44
TSHR P16473 2/20 0.44
KDM4E B2RXH2 1/20 0.44
ALDH1A1 P00352 1/20 0.44
LMNA P02545 1/20 0.44
MMP9 P14780 1/20 0.44
ALOX15 P16050 1/20 0.44
DUT P33316 2/20 0.36
CA12 O43570 1/20 0.33
CA1 P00915 1/20 0.33
CA2 P00918 1/20 0.33
CA9 Q16790 1/20 0.33
CA14 Q9ULX7 1/20 0.33

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
SCHEMBL31171203 0.94 DUT (0.40) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL12013275 0.94 DUT (0.40) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL16898660 0.94 DUT (0.40) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL10982965 0.88 KDM4E (0.52) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL10949282 0.88 KDM4E (0.58) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL10943473 0.86 TSHR (0.56) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL2152291 0.86 KDM4E (0.40) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL10990981 0.86 TSHR (0.56) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL1143263 0.86 TSHR (0.56) USP2TSHRKDM4EALDH1A1LMNA
SCHEMBL4235404 0.86 TSHR (0.56) USP2TSHRKDM4EALDH1A1LMNA

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-9938297-B2 Process for the synthesis of everolimus and intermediates thereof Cipia Limited (IN) 2018-04-10 US disclosed
US-20170217988-A1 Process for the Synthesis of Everolimus and Intermediates Thereof CIPLA LIMITED (IN) 2017-08-03 US disclosed
CN-101367794-B Preparation method for quinazoline derivants and medical uses thereof SHANGHAI HENGRUI PHARM CO LTD 2013-07-10 CN disclosed
EP-1061062-B1 PROCESS FOR PRODUCING BUTANETRIOL DERIVATIVES DAISO CO LTD (JP) 2009-02-18 EP disclosed
CN-101367794-A Preparation method for quinazoline derivants and medical uses thereof SHANGHAI HENGRUI PHARM CO LTD (CN) 2009-02-18 CN disclosed
US-20040024261-A1 Process for preparing butanetriol derivative DAISO CO., LTD. (JP) 2004-02-05 US disclosed
US-6620977-B1 Reacting 1,2,4-butanetriol in multiple steps with specified reagents using selective protection and deprotection of hydroxyl groups DAISO CO., LTD. (JP) 2003-09-16 US disclosed
EP-1061062-A1 PROCESS FOR PRODUCING BUTANETRIOL DERIVATIVE DAISO CO., LTD. (JP) 2000-12-20 EP disclosed
EP-0140307-A2 7-Oxabicycloheptane ethers E.R. Squibb & Sons, Inc. (US) 1985-05-08 EP disclosed
US-4513103-A 7-Oxabicycloheptane ethers useful in the treatment of thrombolytic disease E. R. SQUIBB & SONS, INC. (US) 1985-04-23 US 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 (2 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-20170217988-A1 Process for the Synthesis of Everolimus and Intermediates Thereof MTOR, RICTOR, RPTOR USP2 4476/4885TSHR 4306/4885KDM4E 975/4885
US-20040024261-A1 Process for preparing butanetriol derivative CYP4B1, CYP11B2, CYP11B1 USP2 1419/4885TSHR 2183/4885KDM4E 2328/4885

“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.