SCHEMBL3210075

SCHEMBL3210075

N#CC(=C1CCCC1)c1ccccc1

nearest known ligand 0.50

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
NPC1 O15118 6/20 0.50
RAB9A P51151 6/20 0.50
MAPT P10636 5/20 0.50
SMN1; SMN2 Q16637 5/20 0.50
CYP1A2 P05177 3/20 0.50
CYP2C9 P11712 3/20 0.50
CYP2C19 P33261 3/20 0.50
CYP3A4 P08684 2/20 0.50
RECQL P46063 1/20 0.50
CHRNB2 P17787 1/20 0.44
CHRNA4 P43681 1/20 0.44
ALDH1A1 P00352 7/20 0.43
HPGD P15428 3/20 0.43
MEN1 O00255 3/20 0.43
KMT2A Q03164 3/20 0.43
TSHR P16473 2/20 0.43
NPSR1 Q6W5P4 2/20 0.43
HCRTR1 O43613 1/20 0.43
USP2 O75604 1/20 0.43
TP53 P04637 1/20 0.43

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
SCHEMBL586754 0.98 NPC1 (0.49) NPC1RAB9AMAPTSMN1; SMN2CYP1A2
Benzene SCHEMBL28160719 0.98 NPC1 (0.49) NPC1RAB9AMAPTSMN1; SMN2CYP1A2
Phenylethyl Alcohol SCHEMBL28050164 0.84 TDP1 (0.47) NPC1RAB9AMAPTSMN1; SMN2CYP1A2
SCHEMBL1472474 0.82 CHRNB2 (0.41) NPC1RAB9AMAPTSMN1; SMN2CYP1A2
SCHEMBL2402920 0.82 ALDH1A1 (0.46) NPC1RAB9AMAPTSMN1; SMN2CYP1A2
SCHEMBL28626730 0.80 CYP19A1 (0.43) NPC1RAB9AMAPTSMN1; SMN2CYP1A2
SCHEMBL12320787 0.80 CHRNB2 (0.45) NPC1RAB9AMAPTSMN1; SMN2CYP1A2
SCHEMBL7602039 0.80 SETD7 (0.61) RAB9ACYP1A2CYP2C9CYP2C19CHRNB2
SCHEMBL29090498 0.79 RAB9A (0.51) NPC1RAB9AMAPTSMN1; SMN2CYP1A2
SCHEMBL31512564 0.79 OGG1 (0.39) NPC1RAB9AMAPTSMN1; SMN2CYP1A2

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-20160346181-A1 ORGANIC COMPOUNDS GIVAUDAN SA (CH) 2016-12-01 US claimed
EP-1968531-B1 TOPICAL COMPOSITIONS FOR REDUCING SKIN IRRITATION GIVAUDAN SA (CH) 2014-12-31 EP claimed
CN-101262843-B Improvements in or related to organic compounds GIVAUDAN SA 2013-01-30 CN claimed
US-20120184513-A1 Organic Compounds GIVAUDAN SA (CH) 2012-07-19 US claimed
US-20100063011-A1 Organic compounds GIVAUDAN SA (CH) 2010-03-11 US claimed
EP-1968531-A2 TOPICAL COMPOSITIONS FOR REDUCING SKIN IRRITATION Givaudan SA (CH) 2008-09-17 EP claimed
CN-101262843-A Improvements in or related to organic compounds GIVAUDAN SA (CH) 2008-09-10 CN claimed
WO-2007030961-A2 TOPICAL COMPOSITIONS FOR REDUCING SKIN IRRITATION GIVAUDAN SA (CH) 2007-03-22 WO claimed
CN-116903494-A Preparation method of alpha-alkyl nitrile derivative and alpha-alkenyl nitrile derivative 浙江工业大学 2023-10-20 CN disclosed
CN-109415306-A The preparation method of 2- cyclohexylidene -2- phenylacetonitrile and its odorous analogue 阿甘香气及精细化学有限公司 2019-03-01 CN disclosed
US-20160346181-A1 ORGANIC COMPOUNDS GIVAUDAN SA (CH) 2016-12-01 US disclosed
US-9440097-B2 Organic compounds GIVAUDAN SA (CH) 2016-09-13 US disclosed
EP-1968531-B1 TOPICAL COMPOSITIONS FOR REDUCING SKIN IRRITATION GIVAUDAN SA (CH) 2014-12-31 EP disclosed
CN-101262843-B Improvements in or related to organic compounds GIVAUDAN SA 2013-01-30 CN disclosed
US-7390772-B2 1-phenyl-spiro[2.5]octane-1-carbonitrile analogues their use in fragrance formulations INTERNATIONAL FLAVOR & FRAGRANCES INC. (US) 2008-06-24 US disclosed
US-20070270328-A1 1-PHENYL-SPIRO[2.5]OCTANE-1-CARBONITRILE ANALOGUES THEIR USE IN FRAGRANCE FORMULATIONS INTERNATIONAL FLAVORS & FRAGRANCES INC. 2007-11-22 US disclosed
US-20070270328-A1 1-PHENYL-SPIRO[2.5]OCTANE-1-CARBONITRILE ANALOGUES THEIR USE IN FRAGRANCE FORMULATIONS INTERNATIONAL FLAVORS & FRAGRANCES INC. 2007-11-22 US disclosed
US-20070270328-A1 1-PHENYL-SPIRO[2.5]OCTANE-1-CARBONITRILE ANALOGUES THEIR USE IN FRAGRANCE FORMULATIONS INTERNATIONAL FLAVORS & FRAGRANCES INC. 2007-11-22 US disclosed
EP-1857437-A1 1-Phenyl-spiro[2.5]octane-1-carbonitrile analogues and their use in fragrance formulations INTERNATIONAL FLAVORS & FRAGRANCES, INC. (US) 2007-11-21 EP disclosed
WO-2007030961-A2 TOPICAL COMPOSITIONS FOR REDUCING SKIN IRRITATION GIVAUDAN SA (CH) 2007-03-22 WO 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 (3 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-20100063011-A1 Organic compounds CYP1A1, CYP1B1, OXER1 NPC1 1743/4885RAB9A 4769/4885MAPT 3556/4885
US-20120184513-A1 Organic Compounds CYP1A1, CYP1B1, OXER1 NPC1 1743/4885RAB9A 4769/4885MAPT 3556/4885
US-20160346181-A1 ORGANIC COMPOUNDS CYP1A1, CYP1B1, OXER1 NPC1 1743/4885RAB9A 4769/4885MAPT 3556/4885

“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.