SCHEMBL9933229

SCHEMBL9933229

C#CC(O)(c1ccccc1)c1ccc(OCCCC)cc1

nearest known ligand 0.51

Predicted protein targets (top 13)

geneUniProtsupporting neighboursconfidence
LTA4H P09960 3/20 0.51
MEN1 O00255 5/20 0.48
KMT2A Q03164 4/20 0.48
SMN1; SMN2 Q16637 1/20 0.44
KDM4E B2RXH2 3/20 0.44
ALDH1A1 P00352 2/20 0.44
HTT P42858 1/20 0.44
NPC1 O15118 1/20 0.43
RAB9A P51151 1/20 0.43
NR5A1 Q13285 1/20 0.42
TP53 P04637 1/20 0.42
TSHR P16473 1/20 0.42
POLB P06746 1/20 0.42

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
SCHEMBL28365758 1.00 LTA4H (0.51) LTA4HMEN1KMT2ASMN1; SMN2KDM4E
SCHEMBL10262594 0.94 LTA4H (0.47) LTA4HSMN1; SMN2ALDH1A1RAB9ANR5A1
SCHEMBL25877173 0.89 NR5A1 (0.56) LTA4HNPC1RAB9ANR5A1TP53
SCHEMBL1818269 0.88 AHR (0.43) LTA4HSMN1; SMN2ALDH1A1NR5A1TSHR
SCHEMBL28370253 0.88 AHR (0.43) LTA4HSMN1; SMN2ALDH1A1NR5A1TSHR
SCHEMBL15763651 0.88 LTA4H (0.42) LTA4HMEN1KMT2ASMN1; SMN2ALDH1A1
SCHEMBL1812486 0.88 KIF11 (0.49) LTA4HMEN1KMT2ASMN1; SMN2KDM4E
SCHEMBL10261885 0.87 LTA4H (0.47) LTA4HMEN1KMT2AALDH1A1HTT
SCHEMBL1959801 0.87 FAAH (0.47) LTA4HSMN1; SMN2KDM4EALDH1A1NR5A1
SCHEMBL719359 0.86 ALDH1A1 (0.55) LTA4HMEN1KMT2ASMN1; SMN2KDM4E

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
EP-3621958-B9 PHOTOCHROMIC INDENO FUSED PHENANTHRENOPYRAN COMPOUNDS TRANSITIONS OPTICAL LTD (IE) 2024-09-25 EP disclosed
EP-3621958-B1 PHOTOCHROMIC INDENO FUSED PHENANTHRENOPYRAN COMPOUNDS TRANSITIONS OPTICAL LTD (IE) 2024-07-10 EP disclosed
CN-113150007-B Photochromic indeno-fused ring pyran compounds 光学转变公司 2024-03-08 CN disclosed
CN-110730778-B Photochromic indeno-fused phenanthropyran compounds 光学转变有限公司 2023-09-12 CN disclosed
US-11453654-B2 Photochromic indeno fused phenanthrenopyran compounds TRANSITIONS OPTICAL, LTD. (IE) 2022-09-27 US 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
US-20210317129-A1 Indolenaphthopyrans TRANSITIONS OPTICAL, LTD. (IE) 2021-10-14 US disclosed
EP-3071576-B1 PHOTOCHROMIC INDENO-FUSED RING PYRAN COMPOUNDS TRANSITIONS OPTICAL INC (US) 2021-08-18 EP disclosed
CN-113227099-A Articles comprising indole naphthopyrans 光学转变有限公司 2021-08-06 CN disclosed
US-20150141661-A1 Photochromic Indeno-Fused Ring Pyran Compounds TRANSITIONS OPTICAL, INC. (US) 2015-05-21 US disclosed
US-20150141663-A1 Fused Ring Indeno Compounds For Preparation Of Photochromic Compounds TRANSITIONS OPTICAL, INC. (US) 2015-05-21 US disclosed
US-20150141662-A1 Method Of Preparing Fused Ring Indeno Compounds TRANSITIONS OPTICAL, INC. (US) 2015-05-21 US disclosed
EP-2651914-B1 PHOTOCHROMIC COMPOUNDS AND COMPOSITIONS TRANSITIONS OPTICAL INC (US) 2015-05-13 EP disclosed
US-9029565-B1 Fused ring indeno compounds for preparation of photochromic compounds TRANSITIONS OPTICAL, INC. (US) 2015-05-12 US disclosed
US-8920928-B2 Photochromic compounds and compositions TRANSITIONS OPTICAL, INC. (US) 2014-12-30 US disclosed
EP-2651914-A1 PHOTOCHROMIC COMPOUNDS AND COMPOSITIONS Transitions Optical, Inc. (US) 2013-10-23 EP disclosed
WO-2012082999-A1 PHOTOCHROMIC COMPOUNDS AND COMPOSITIONS TRANSITIONS OPTICAL, INC. (US) 2012-06-21 WO disclosed
US-20120156508-A1 PHOTOCHROMIC COMPOUNDS AND COMPOSITIONS TRANSITIONS OPTICAL, INC. (US) 2012-06-21 US disclosed
US-20120153333-A1 Light-Emitting Device and Lighting Device SEMICONDUCTOR ENERGY LABORATORY CO., LTD. 2012-06-21 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-20150141662-A1 Method Of Preparing Fused Ring Indeno Compounds INHA, INTS9, CA9 LTA4H 283/4885MEN1 657/4885KMT2A 1445/4885
US-20150141663-A1 Fused Ring Indeno Compounds For Preparation Of Photochromic Compounds IPO5, INCENP, NQO1 LTA4H 1836/4885MEN1 2514/4885KMT2A 1702/4885
US-20210317129-A1 Indolenaphthopyrans AHR, TDO2, TPH2 LTA4H 2688/4885MEN1 3107/4885KMT2A 2760/4885
US-20150141661-A1 Photochromic Indeno-Fused Ring Pyran Compounds INF2, INCENP, RB1 LTA4H 2078/4885MEN1 1330/4885KMT2A 1384/4885
US-11453654-B2 Photochromic indeno fused phenanthrenopyran compounds ALDH1A2, RB1, INCENP LTA4H 1820/4885MEN1 1633/4885KMT2A 1736/4885
US-20120156508-A1 PHOTOCHROMIC COMPOUNDS AND COMPOSITIONS CRY2, CRY1, IPO4 LTA4H 691/4885MEN1 3275/4885KMT2A 2088/4885

“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.