SCHEMBL8640905

SCHEMBL8640905

COC(=O)[C@H]1O[C@H](COCc2ccccc2)[C@@H]1OCc1ccccc1

nearest known ligand 0.50

Predicted protein targets (top 15)

geneUniProtsupporting neighboursconfidence
▸ TACR2 P21452 3/20 0.48
▸ NT5E P21589 1/20 0.48
▸ PTPN1 P18031 8/20 0.46
▸ CDC25B P30305 5/20 0.46
▸ SSTR4 P31391 2/20 0.45
▸ SSTR1 P30872 1/20 0.45
▸ SSTR2 P30874 1/20 0.45
▸ SSTR3 P32745 1/20 0.45
▸ SSTR5 P35346 1/20 0.45
▸ PTPN2 P17706 4/20 0.44
▸ HTR1A P08908 1/20 0.44
▸ PTPN11 Q06124 3/20 0.44
▸ PTPN6 P29350 2/20 0.44
▸ GJB2 P29033 1/20 0.44
▸ BCHE P06276 1/20 0.44

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
SCHEMBL22288949 0.83 TACR2 (0.52) TACR2NT5EPTPN1CDC25BSSTR4
SCHEMBL7151712 0.82 TACR2 (0.51) TACR2NT5EPTPN1CDC25BSSTR4
SCHEMBL13956411 0.82 TACR2 (0.47) TACR2PTPN1CDC25BSSTR4SSTR1
SCHEMBL8723296 0.82 NT5E (0.53) TACR2NT5EPTPN1CDC25BSSTR4
SCHEMBL13956413 0.81 PTPN1 (0.41) TACR2NT5EPTPN1CDC25BSSTR4
SCHEMBL20473776 0.81 PTPN1 (0.50) TACR2NT5EPTPN1CDC25BSSTR4
SCHEMBL28516241 0.81 PTPN1 (0.50) TACR2NT5EPTPN1CDC25BSSTR4
SCHEMBL22288956 0.80 TACR2 (0.47) TACR2NT5EPTPN1CDC25BSSTR4
SCHEMBL30712002 0.80 NT5E (0.48) TACR2NT5EPTPN1CDC25BPTPN2
SCHEMBL9699456 0.79 PDPK1 (0.44) PTPN1SSTR4SSTR1SSTR2SSTR3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-5750735-A CHEMICAL INTERMEDIATES FOR ANTIBIOTICS AMERICAN CYANAMID COMPANY (US) 1998-05-12 — — US disclosed
US-5744465-A Method of inhibiting a β-lactamase enzyme by administering novel 2-thiosubstituted carbapenems AMERICAN CYANAMID COMPANY (US) 1998-04-28 — — US disclosed
US-5623081-A USING BENZYLOXYACETALDEHYDE DIMETHYL ETHER, HALOGENATED 1-PHENYLMETHOXY-4-PENTEN-2-OL; CYCLIZATION LIN YANG-I (US) 1997-04-22 — — US disclosed
US-5602118-A A 2-((2-SUBSTITUTED ALKYL)FUR-3-YL)-THIO-),3-CARBOXY-2-CARBOPENEM DERIVATIVES; EFFECTIVE AGAINST BETA-LACTAM ANTIBIOTIC-RESISTANT BACTERIA AMERICAN CYANAMID COMPANY (US) 1997-02-11 — — US disclosed
EP-0617036-A2 Novel 2-thiosubstituted carbapenems AMERICAN CYANAMID COMPANY (US) 1994-09-28 — — EP disclosed
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