Results for:
chemical Classification: Tricyclo

Compound Details

Synonymous names	(?)-Kelsoene CHEMBL400313 345910-50-1
IUPAC name
SMILES	CC1CCC2C1C(C3C2(CC3)C)C(=C)C
Inchi	InChI=1S/C15H24/c1-9(2)13-12-7-8-15(12,4)11-6-5-10(3)14(11)13/h10-14H,1,5-8H2,2-4H3/t10-,11+,12+,13-,14-,15-/m1/s1
Formula	C15H24
PubChem ID	10726904
Molweight	204.357
LogP	4.15
Atoms	39
Bonds	41
H-bond Acceptor	0
H-bond Donor	0
Chemical Classification	Terpenes Tricyclo

mVOC Specific Details

Microorganisms emitting the compound	Kingdom Species Biological Function Origin/Habitat Reference Bacteria Streptomyces Caviscabies n/a Schulz and Dickschat, 2007 Bacteria Streptomyces Sp. GWS-BW-H5. n/a Dickschat et al., 2005_2
Method	Kingdom Species Growth Medium Applied Method Verification Bacteria Streptomyces Caviscabies n/a n/a Bacteria Streptomyces Sp. GWS-BW-H5. n/a n/a

(1aR,4R,4aR,7bS)-1,1,4,7-tetramethyl-1a,2,3,4,4a,5,6,7b-octahydrocyclopropa[e]azulene

Compound Details

Synonymous names	alpha-Grujunene alpha-Gurjunene C19734 DTXSID0052126 CHEBI:61699 (-)-alpha-Gurjunene ZINC59200506 FT-0632212 489-40-7 (1aR,4R,4aR,7bS)-1,1,4,7-tetramethyl-1a,2,3,4,4a,5,6,7b-octahydro-1H-cyclopropa[e]azulene
IUPAC name	(1aR,4R,4aR,7bS)-1,1,4,7-tetramethyl-1a,2,3,4,4a,5,6,7b-octahydrocyclopropa[e]azulene
SMILES	CC1CCC2C(C2(C)C)C3=C(CCC13)C
Inchi	InChI=1S/C15H24/c1-9-6-8-12-14(15(12,3)4)13-10(2)5-7-11(9)13/h9,11-12,14H,5-8H2,1-4H3/t9-,11-,12-,14-/m1/s1
Formula	C15H24
PubChem ID	15560276
Molweight	204.357
LogP	4.04
Atoms	39
Bonds	41
H-bond Acceptor	0
H-bond Donor	0
Chemical Classification	Terpenes Tricyclo Alkenes

mVOC Specific Details

Microorganisms emitting the compound	Kingdom Species Biological Function Origin/Habitat Reference Bacteria Streptomyces Caviscabies n/a Schulz and Dickschat, 2007
Method	Kingdom Species Growth Medium Applied Method Verification Bacteria Streptomyces Caviscabies n/a n/a

(4aS,7aS,7bR)-3,6,6,7b-tetramethyl-2,4,4a,5,7,7a-hexahydro-1H-cyclobuta[e]indene

Compound Details

Synonymous names	FBSBGGJQVUYUDB-ZLDLUXBVSA-N Delta6-Protoilludene 6-protoilludene Protoillud-6-ene Delta(6)-protoilludene C20476 CHEBI:68655 (3aS)-2,2,5,7beta-Tetramethyl-6,7-ethano-3aalpha,4,7,7aalpha-tetrahydroindan (4aS,7aS,7bR)-3,6,6,7b-tetramethyl-2,4,4a,5,6,7,7a,7b-octahydro-1H-cyclobuta[e]indene (4aS,7aS,7bR)-3,6,6,7b-Tetramethyl-2,4,4a,5,6,7,7a,7b-octahydro-1H-cyclobuta[1,2-e]indene InChI=1/C15H24/c1-10-7-11-8-14(2,3)9-13(11)15(4)6-5-12(10)15/h11,13H,5-9H2,1-4H3/t11-,13+,15+/m1/s
IUPAC name	(4aS,7aS,7bR)-3,6,6,7b-tetramethyl-2,4,4a,5,7,7a-hexahydro-1H-cyclobuta[e]indene
SMILES	CC1=C2CCC2(C3CC(CC3C1)(C)C)C
Inchi	InChI=1S/C15H24/c1-10-7-11-8-14(2,3)9-13(11)15(4)6-5-12(10)15/h11,13H,5-9H2,1-4H3/t11-,13+,15+/m1/s1
Formula	C15H24
PubChem ID	15939655
Molweight	204.357
LogP	4.06
Atoms	39
Bonds	41
H-bond Acceptor	0
H-bond Donor	0
Chemical Classification	Terpenes Tricyclo Alkenes

mVOC Specific Details

Microorganisms emitting the compound	Kingdom Species Biological Function Origin/Habitat Reference Fungi Fomitopsis Pinicola na Germany Rösecke et al., 2000 Bacteria Streptomyces UC5319 n/a Schulz and Dickschat, 2007
Method	Kingdom Species Growth Medium Applied Method Verification Fungi Fomitopsis Pinicola na GC/MS No Bacteria Streptomyces UC5319 n/a n/a