SCHEMBL6073558

SCHEMBL6073558

CC(C)(C)c1ccc2c(c1)C(C)(C)CC2

nearest known ligand 0.40

Predicted protein targets (top 20)

geneUniProtsupporting neighboursconfidence
RXRA P19793 7/20 0.40
RXRB P28702 4/20 0.40
ALDH1A1 P00352 3/20 0.36
HPGD P15428 1/20 0.36
ALOX15 P16050 1/20 0.36
HSD17B10 Q99714 1/20 0.36
TDP1 Q9NUW8 1/20 0.36
RXRG P48443 4/20 0.35
HTR2A P28223 1/20 0.34
HTR2C P28335 1/20 0.34
MEN1 O00255 1/20 0.33
GAA P10253 1/20 0.33
MAPT P10636 1/20 0.33
PKM P14618 1/20 0.33
RECQL P46063 1/20 0.33
KMT2A Q03164 1/20 0.33
PPARA Q07869 1/20 0.33
KIF11 P52732 1/20 0.33
TSHR P16473 1/20 0.32
KDM1A O60341 1/20 0.32

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
SCHEMBL30859520 1.00 RXRA (0.40) RXRARXRBALDH1A1HPGDALOX15
SCHEMBL30859519 1.00 RXRA (0.40) RXRARXRBALDH1A1HPGDALOX15
SCHEMBL17563594 0.81 CYP11B2 (0.40) RXRARXRBALDH1A1HPGDALOX15
SCHEMBL17563596 0.81 CYP11B2 (0.40) RXRARXRBALDH1A1HPGDALOX15
SCHEMBL17563595 0.81 CYP11B2 (0.40) RXRARXRBALDH1A1HPGDALOX15
SCHEMBL24401065 0.79 KIF11 (0.36) ALDH1A1HPGDALOX15HSD17B10TDP1
SCHEMBL24648694 0.75 HSPA9 (0.52) RXRARXRBALDH1A1HPGDALOX15
SCHEMBL25100748 0.74 MAP3K14 (0.36) RXRARXRBALDH1A1HPGDALOX15
SCHEMBL22589962 0.74 ESR1 (0.35) RXRARXRBALDH1A1RXRGHTR2A
SCHEMBL9770689 0.74 CYP3A4 (0.41) RXRARXRBALDH1A1ALOX15TDP1

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

PatentTitleAssigneePublishedPriorityFilingCountryStatus
CN-117486697-A Synthetic method of salix musk 安徽金禾化学材料研究所有限公司 2024-02-02 CN claimed
CN-111285750-B Device and method for continuous flow synthesis of 1,1-dimethyl-6-tert-butyl indan 天门市德远化工科技有限公司 2022-12-06 CN claimed
CN-111285750-A Device and method for continuous flow synthesis of 1, 1-dimethyl-6-tert-butyl indan 天门市德远化工科技有限公司 2020-06-16 CN claimed
US-20030191145-A1 Unsaturated derivatives at the 4-position of 6-tert-butyl-1,1-dimethylindane and their use in human and veterinary medicine and in cosmetics GALDERMA RESEARCH & DEVELOPMENT (FR) 2003-10-09 US claimed
US-6534545-B1 Unsaturated derivatives at the 4-position of 6-tert-butyl-1,1-dimethylindane and their use in human and veterinary medicine and cosmetics GALDERMA RESEARCH & DEVELOPMENT (FR) 2003-03-18 US claimed
EP-0905118-B1 Unsaturated 6-tert-butyl-1,1-dimethylindane derivates substituted in the 4-position and their use in human and veterinary medicine as well as in cosmetics GALDERMA RES & DEV (FR) 2001-08-16 EP claimed
US-6180674-B1 THERAPY FOR SKIN DISORDERS GALDERMA RESEARCH & DEVELOPMENT (FR) 2001-01-30 US claimed
EP-0905118-A1 Unsaturated 6-tert-butyl-1,1-dimethylindane derivates substituted in the 4-position and their use in human and veterinary medicine as well as in cosmetics Galderma Research & Development, S.N.C. (FR) 1999-03-31 EP claimed
CN-117486697-A Synthetic method of salix musk 安徽金禾化学材料研究所有限公司 2024-02-02 CN disclosed
CN-117486697-A Synthetic method of salix musk 安徽金禾化学材料研究所有限公司 2024-02-02 CN disclosed
CN-111285750-B Device and method for continuous flow synthesis of 1,1-dimethyl-6-tert-butyl indan 天门市德远化工科技有限公司 2022-12-06 CN disclosed
CN-111285750-B Device and method for continuous flow synthesis of 1,1-dimethyl-6-tert-butyl indan 天门市德远化工科技有限公司 2022-12-06 CN disclosed
CN-111285750-B Device and method for continuous flow synthesis of 1,1-dimethyl-6-tert-butyl indan 天门市德远化工科技有限公司 2022-12-06 CN disclosed
WO-2020150668-A1 COMPOSITIONS AND METHODS FOR IMMUNE MODULATION AND TREATMENT OF CANCER BOARD OF TRUSTEES OF MICHIGAN STATE UNIVERSITY (US) 2020-07-23 WO disclosed
WO-1998007813-A2 LAUNDRY DETERGENT COMPOSITIONS COMPRISING β-KETOESTER PRO-FRAGRANCES THE PROCTER & GAMBLE COMPANY (US) 1998-02-26 WO disclosed
US-4987261-A Diaminoindane derivatives MITSUI TOATSU CHEMICALS, INC. (JP) 1991-01-22 US disclosed
EP-0040338-A2 Process for the preparation of acylated indanes and tetrahydronaphthalenes INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) 1981-11-25 EP disclosed
US-4178311-A Process for the production of compounds useful in perfumery INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) 1979-12-11 US disclosed
EP-0004914-A1 Process for the production of compounds useful in perfumery INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) 1979-10-31 EP disclosed
US-4162256-A Process for the production of compounds useful in perfumery INTERNATIONAL FLAVORS & FRAGRANCES INC. (US) 1979-07-24 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 (1 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-20030191145-A1 Unsaturated derivatives at the 4-position of 6-tert-butyl-1,1-dimethylindane and their use in human and veterinary medicine and in cosmetics REL, DERL1, TLR7 RXRA 30/4885RXRB 44/4885ALDH1A1 491/4885

“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.