SCHEMBL17256253

SCHEMBL17256253

C#CCOCC(COCC#C)(COCC#C)NC(=O)O

nearest known ligand 0.41

Predicted protein targets (top 5)

geneUniProtsupporting neighboursconfidence
TSHR P16473 1/20 0.41
SLC1A3 P43003 1/20 0.32
SLC1A2 P43004 1/20 0.32
SLC1A1 P43005 1/20 0.32
POLB P06746 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
SCHEMBL18227311 0.82 TSHR (0.36) TSHR
SCHEMBL18240013 0.81 TSHR (0.39) TSHRSLC1A3SLC1A2SLC1A1
SCHEMBL19249813 0.79 TSHR (0.42) TSHR
SCHEMBL19610499 0.78 TSHR (0.33) TSHR
SCHEMBL21291238 0.78 TSHR (0.53) TSHRPOLB
SCHEMBL19249286 0.77 L3MBTL1 (0.37) TSHR
SCHEMBL17268906 0.77 CTSK (0.35) TSHR
SCHEMBL25764177 0.76 TSHR (0.46) TSHR
SCHEMBL19153446 0.74 KDM4E (0.35) TSHR
SCHEMBL19249812 0.74 HRH3 (0.40) TSHR

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20230398224-A1 TARGETED PLASMA PROTEIN DEGRADATION NOVARTIS AG (CH) 2023-12-14 US disclosed
EP-4100064-A1 TARGETED PLASMA PROTEIN DEGRADATION Novartis AG (CH) 2022-12-14 EP disclosed
WO-2021156792-A1 TARGETED PLASMA PROTEIN DEGRADATION NOVARTIS AG (CH) 2021-08-12 WO disclosed
US-10851367-B2 Tissue-specific genome engineering using CRISPR-Cas9 PFIZER INC. (US) 2020-12-01 US disclosed
EP-3145934-B1 SUBSTITUTED-6,8-DIOXABICYCLO[3.2.1]OCTANE-2,3-DIOL COMPOUNDS AS TARGETING AGENTS OF ASGPR PFIZER (US) 2020-11-11 EP disclosed
US-10813942-B2 Substituted-6,8-dioxabicyclo[3.2.1]octane-2,3-diol compounds as targeting agents of ASGPR PFIZER INC. (US) 2020-10-27 US disclosed
US-20190321382-A1 SUBSTITUTED-6,8-DIOXABICYCLO[3.2.1]OCTANE-2,3-DIOL COMPOUNDS AS TARGETING AGENTS OF ASGPR PFIZER INC. (US) 2019-10-24 US disclosed
US-10376531-B2 Substituted-6,8-dioxabicyclo[3.2.1]octane-2,3-diol compounds as targeting agents of ASGPR PFIZER INC. (US) 2019-08-13 US disclosed
US-20180296585-A1 SUBSTITUTED-6,8-DIOXABICYCLO[3.2.1]OCTANE-2,3-DIOL COMPOUNDS AS TARGETING AGENTS OF ASGPR PFIZER INC. (US) 2018-10-18 US disclosed
EP-3373979-A1 TISSUE-SPECIFIC GENOME ENGINEERING USING CRISPR-CAS9 Pfizer Inc (US) 2018-09-19 EP disclosed
US-10039778-B2 Substituted-6,8-dioxabicyclo[3.2.1]octane-2,3-diol compounds as targeting agents of ASGPR PFIZER INC. (US) 2018-08-07 US disclosed
WO-2017083368-A9 TISSUE-SPECIFIC GENOME ENGINEERING USING CRISPR-CAS9 PFIZER INC. (US) 2018-04-12 WO disclosed
US-20170165284-A1 SUBSTITUTED-6,8-DIOXABICYCLO[3.2.1]OCTANE-2,3-DIOL COMPOUNDS AS TARGETING AGENTS OF ASGPR PFIZER INC. (US) 2017-06-15 US disclosed
WO-2017083368-A1 TISSUE-SPECIFIC GENOME ENGINEERING USING CRISPR-CAS9 PFIZER INC. (US) 2017-05-18 WO disclosed
US-20170137801-A1 TISSUE-SPECIFIC GENOME ENGINEERING USING CRISPR-CAS9 THE REGENTS OF THE UNIVERSITY OF CALIFORNIA 2017-05-18 US disclosed
US-9617293-B2 Substituted-6,8-dioxabicyclo[3.2.1]octane-2,3-diol compounds as targeting agents of ASGPR PFIZER INC. (US) 2017-04-11 US disclosed
US-20160207953-A1 SUBSTITUTED-6,8-DIOXABICYCLO[3.2.1]OCTANE-2,3-DIOL COMPOUNDS AS TARGETING AGENTS OF ASGPR PFIZER INC. (US) 2016-07-21 US disclosed
US-9340553-B2 Substituted-6,8-dioxabicyclo[3.2.1]octane-2,3-diol compounds as targeting agents of ASGPR PFIZER INC. (US) 2016-05-17 US disclosed
US-20150329555-A1 SUBSTITUTED-6,8-DIOXABICYCLO[3.2.1]OCTANE-2,3-DIOL COMPOUNDS AS TARGETING AGENTS OF ASGPR PFIZER INC. (US) 2015-11-19 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 (10 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-20160207953-A1 SUBSTITUTED-6,8-DIOXABICYCLO[3.2.1]OCTANE-2,3-DIOL COMPOUNDS AS TARGETING AGENTS OF ASGPR ASGR1, MRGPRX2, LDLR TSHR 319/4885SLC1A3 1654/4885SLC1A2 1603/4885
US-20170165284-A1 SUBSTITUTED-6,8-DIOXABICYCLO[3.2.1]OCTANE-2,3-DIOL COMPOUNDS AS TARGETING AGENTS OF ASGPR ASGR1, MRGPRX2, LDLR TSHR 319/4885SLC1A3 1654/4885SLC1A2 1603/4885
US-20150329555-A1 SUBSTITUTED-6,8-DIOXABICYCLO[3.2.1]OCTANE-2,3-DIOL COMPOUNDS AS TARGETING AGENTS OF ASGPR ASGR1, MRGPRX2, LDLR TSHR 319/4885SLC1A3 1654/4885SLC1A2 1603/4885
US-10813942-B2 Substituted-6,8-dioxabicyclo[3.2.1]octane-2,3-diol compounds as targeting agents of ASGPR ASGR1, MRGPRX2, LDLR TSHR 319/4885SLC1A3 1654/4885SLC1A2 1603/4885
US-10851367-B2 Tissue-specific genome engineering using CRISPR-Cas9 ASGR1, LDLR, HAVCR2 TSHR 823/4885SLC1A3 3855/4885SLC1A2 3636/4885
US-20190321382-A1 SUBSTITUTED-6,8-DIOXABICYCLO[3.2.1]OCTANE-2,3-DIOL COMPOUNDS AS TARGETING AGENTS OF ASGPR ASGR1, MRGPRX2, LDLR TSHR 319/4885SLC1A3 1654/4885SLC1A2 1603/4885
US-20180296585-A1 SUBSTITUTED-6,8-DIOXABICYCLO[3.2.1]OCTANE-2,3-DIOL COMPOUNDS AS TARGETING AGENTS OF ASGPR ASGR1, MRGPRX2, LDLR TSHR 319/4885SLC1A3 1654/4885SLC1A2 1603/4885
US-10039778-B2 Substituted-6,8-dioxabicyclo[3.2.1]octane-2,3-diol compounds as targeting agents of ASGPR ASGR1, MRGPRX2, LDLR TSHR 319/4885SLC1A3 1654/4885SLC1A2 1603/4885
US-10376531-B2 Substituted-6,8-dioxabicyclo[3.2.1]octane-2,3-diol compounds as targeting agents of ASGPR ASGR1, MRGPRX2, LDLR TSHR 319/4885SLC1A3 1654/4885SLC1A2 1603/4885
US-20230398224-A1 TARGETED PLASMA PROTEIN DEGRADATION M6PR, ASGR1, IGF2R TSHR 452/4885SLC1A3 1818/4885SLC1A2 1472/4885

“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.