SCHEMBL9978095

SCHEMBL9978095

CN1CCC(OC(=O)Oc2ccc(F)cc2)CC1

nearest known ligand 0.63

Predicted protein targets (top 14)

geneUniProtsupporting neighboursconfidence
▸ MAPT P10636 1/20 0.63
▸ SMN1; SMN2 Q16637 1/20 0.63
▸ KMT2A Q03164 2/20 0.52
▸ RAB9A P51151 1/20 0.49
▸ SCN1A P35498 3/20 0.49
▸ SCN2A Q99250 3/20 0.49
▸ SCN3A Q9NY46 3/20 0.49
▸ MEN1 O00255 1/20 0.49
▸ CHRM3 P20309 3/20 0.48
▸ CHRM5 P08912 2/20 0.48
▸ CHRM1 P11229 2/20 0.48
▸ ALDH1A1 P00352 2/20 0.48
▸ CHRM4 P08173 1/20 0.48
▸ SSTR4 P31391 1/20 0.47

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
SCHEMBL313843 0.82 MAPT (0.48) MAPTSMN1; SMN2KMT2ARAB9ASCN1A
SCHEMBL18078975 0.82 MAPT (0.56) MAPTSMN1; SMN2KMT2ARAB9ASCN1A
Hydrochloric Acid SCHEMBL16694536 0.81 ALDH1A1 (0.47) MAPTSMN1; SMN2KMT2ARAB9AMEN1
Iodide SCHEMBL30309833 0.79 SMN1; SMN2 (0.53) MAPTSMN1; SMN2KMT2AALDH1A1SSTR4
SCHEMBL2015133 0.78 SMN1; SMN2 (0.39) MAPTSMN1; SMN2KMT2AMEN1
SCHEMBL1844575 0.78 SCN1A (0.77) MAPTSMN1; SMN2KMT2ASCN1ASCN2A
SCHEMBL10274500 0.77 HRH3 (0.63) MAPTSMN1; SMN2KMT2A
SCHEMBL31215478 0.77 SSTR4 (0.60) MAPTSMN1; SMN2KMT2ARAB9AMEN1
SCHEMBL1023344 0.76 SCN1A (0.53) MAPTSMN1; SMN2KMT2ARAB9ASCN1A
Fumaric Acid SCHEMBL11257173 0.75 HRH1 (0.56) MAPTSMN1; SMN2KMT2AMEN1CHRM3

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3621958-B1 PHOTOCHROMIC INDENO FUSED PHENANTHRENOPYRAN COMPOUNDS TRANSITIONS OPTICAL LTD (IE) 2024-07-10 — — EP disclosed
EP-3268375-B1 PHOTOCHROMIC THIENOCHROMENE COMPOUNDS TRANSITIONS OPTICAL INC (US) 2022-06-15 — — EP disclosed
EP-3071576-B9 PHOTOCHROMIC INDENO-FUSED RING PYRAN COMPOUNDS TRANSITIONS OPTICAL INC (US) 2021-12-22 — — EP disclosed
EP-3071576-B1 PHOTOCHROMIC INDENO-FUSED RING PYRAN COMPOUNDS TRANSITIONS OPTICAL INC (US) 2021-08-18 — — EP disclosed
US-20200048216-A1 Photochromic Indeno Fused Phenanthrenopyran Compounds TRANSITIONS OPTICAL, LTD. (IE) 2020-02-13 — — US disclosed
EP-2370420-B9 PHOTOCHROMIC COMPOUNDS TRANSITIONS OPTICAL INC (US) 2019-11-13 — — EP disclosed
EP-2370420-B1 PHOTOCHROMIC COMPOUNDS TRANSITIONS OPTICAL INC (US) 2019-05-22 — — EP disclosed
EP-2357217-B9 PHOTOCHROMIC COMPOUNDS TRANSITIONS OPTICAL INC (US) 2019-03-13 — — EP disclosed
EP-3071550-B1 METHOD OF PREPARING FUSED RING INDENO COMPOUNDS TRANSITIONS OPTICAL INC (US) 2019-03-13 — — EP disclosed
US-10005763-B2 Photochromic compounds TRANSITIONS OPTICAL, INC. (US) 2018-06-26 — — US disclosed
US-20080096049-A1 capable of switching between the two states in response to at least actinic radiation; thermally reversible TRANSITIONS OPTICAL, INC. (US) 2008-04-24 — — US disclosed
US-20080096049-A1 capable of switching between the two states in response to at least actinic radiation; thermally reversible TRANSITIONS OPTICAL, INC. (US) 2008-04-24 — — US disclosed
US-20080096048-A1 Thermally reversible; absorption ratio greater than 2.3 TRANSITIONS OPTICAL, INC. (US) 2008-04-24 — — US disclosed
US-20080096048-A1 Thermally reversible; absorption ratio greater than 2.3 TRANSITIONS OPTICAL, INC. (US) 2008-04-24 — — US disclosed
US-7342112-B2 Photochromic compounds PPG INDUSTRIES OHIO, INC. (US) 2008-03-11 — — US disclosed
US-7342112-B2 Photochromic compounds PPG INDUSTRIES OHIO, INC. (US) 2008-03-11 — — US disclosed
US-20080051575-A1 capable of switching between the two states in response to at least actinic radiation; thermally reversible TRANSITIONS OPTICAL ,INC. (US) 2008-02-28 — — US disclosed
US-20080051575-A1 capable of switching between the two states in response to at least actinic radiation; thermally reversible TRANSITIONS OPTICAL ,INC. (US) 2008-02-28 — — US disclosed
US-20080045704-A1 Thermally reversible; absorption ratio greater than 2.3; cell method TRANSITIONS OPTICAL, INC. (US) 2008-02-21 — — US disclosed
US-20080045704-A1 Thermally reversible; absorption ratio greater than 2.3; cell method TRANSITIONS OPTICAL, INC. (US) 2008-02-21 — — 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 (6 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-20200048216-A1 Photochromic Indeno Fused Phenanthrenopyran Compounds ALDH1A2, RB1, INCENP MAPT 1822/4885SMN1; SMN2 4769/4885KMT2A 1736/4885
US-20080045704-A1 Thermally reversible; absorption ratio greater than 2.3; cell method CCND3, CCND1, CCND2 MAPT 4145/4885SMN1; SMN2 1316/4885KMT2A 1511/4885
US-20080096048-A1 Thermally reversible; absorption ratio greater than 2.3 CCND1, CCND3, CCND2 MAPT 4150/4885SMN1; SMN2 1502/4885KMT2A 1838/4885
US-10005763-B2 Photochromic compounds CCR4, CCR8, CBR3 MAPT 3402/4885SMN1; SMN2 4001/4885KMT2A 2193/4885
US-20080051575-A1 capable of switching between the two states in response to at least actinic radiation; thermally reversible CCND1, CCND2, CCNE1 MAPT 4085/4885SMN1; SMN2 993/4885KMT2A 1830/4885
US-20080096049-A1 capable of switching between the two states in response to at least actinic radiation; thermally reversible CCND1, CCND2, CCNE1 MAPT 4085/4885SMN1; SMN2 993/4885KMT2A 1830/4885

“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.

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